SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs387673028 | in-del | -/T | | | intron-variant | Asb9 | Mm_Celera | X:164501876 | TTTCTTATTTTTTTT[-/T]CATAGTGACATTTTC | 69299 |
rs387692311 | in-del | -/GTGT | | | intron-variant | Asb9 | Mm_Celera | X:164524862 | TGTGTGTGTGTGTGT[-/GTGT]ATTTGAATGTATTCA | 69299 |
rs387695431 | snp | C/G | | | intron-variant | Asb9 | GRCm38.p3 | X:164537142 | TTTGTTTCTTTCTTT[C/G]TTTGTTTCTTTCTTT | 69299 |
rs387714353 | in-del | -/AAA | | | intron-variant | Asb9 | Mm_Celera | X:164508318 | CCAAAAAAAAAAAAA[-/AAA]TAGGAAGGGATTTTG | 69299 |
rs387741941 | in-del | -/CAGTGCCTGCT | | | upstream-variant-2KB | Asb9 | GRCm38.p3 | X:164497163 | AGATGAAGAACTAGA[-/CAGTGCCTGCT]GAGAGAATCAGTCTT | 69299 |
rs387752725 | in-del | -/GTGT | | | intron-variant | Asb9 | Mm_Celera | X:164507039 | TGTGTGTGTGTGTGT[-/GTGT]ATTATAGGAACACTG | 69299 |
rs387901354 | in-del | -/A | | | intron-variant | Asb9 | Mm_Celera | X:164530282 | AAGTATTGGAAAAAA[-/A]TGGCCTCCATCTTGT | 69299 |
rs578319183 | snp | A/G | | | intron-variant | Asb9 | GRCm38.p3 | X:164529357 | TCAGAGGACCAACCC[A/G]AGGGCACTGCTGCCT | 69299 |
rs578329507 | snp | C/G | | | intron-variant | Asb9 | GRCm38.p3 | X:164517527 | TGATTCTTGATCTTA[C/G]AGCACAAGCCATTGA | 69299 |
rs578417678 | snp | A/T | | | intron-variant | Asb9 | GRCm38.p3 | X:164518262 | TATTTGTGACTATTG[A/T]GAAGGGTGTTGTTTC | 69299 |
rs578484038 | snp | C/T | | | intron-variant | Asb9 | GRCm38.p3 | X:164499547 | ATATATACATATATA[C/T]ATGTATGGATAAATA | 69299 |
rs578681266 | snp | G/T | | | intron-variant | Asb9 | GRCm38.p3 | X:164534336 | TGACCAGGCGACTGG[G/T]CATTGTGTGTGTGTG | 69299 |
rs578685385 | snp | A/G | | | intron-variant | Asb9 | GRCm38.p3 | X:164519530 | ATTTGATTATTTCCT[A/G]CCATCTACTTCTCTT | 69299 |
rs578688660 | snp | A/G | | | upstream-variant-2KB | Asb9 | GRCm38.p3 | X:164497002 | CAAGGTATATCACTA[A/G]CACTTGCTAAAATAG | 69299 |
rs578696447 | snp | A/T | | | intron-variant | Asb9 | GRCm38.p3 | X:164516287 | ACTGGTTAGTTCATA[A/T]TGTTGTTCCACCTAT | 69299 |
rs578715822 | snp | C/T | | | intron-variant | Asb9 | GRCm38.p3 | X:164518723 | GGGTGTTGGATTTTG[C/T]CAAATGCTTTCTCGG | 69299 |
rs578726731 | snp | A/G | | | intron-variant | Asb9 | GRCm38.p3 | X:164526101 | AGTTCTGGGGGTACT[A/G]GTTAGTTCATATTGT | 69299 |
rs578729488 | snp | C/T | | | intron-variant | Asb9 | GRCm38.p3 | X:164499794 | AAGTGTGCACCACTC[C/T]ACCAAAGTATTATCT | 69299 |
rs578738808 | snp | C/T | | | intron-variant | Asb9 | GRCm38.p3 | X:164517146 | TCTCCACATCCTCGA[C/T]AGCATCTGCTGTCAC | 69299 |
rs578898883 | snp | C/G | | | intron-variant | Asb9 | GRCm38.p3 | X:164522855 | ACACACACACACACA[C/G]ACACACACACACACA | 69299 |
rs579044425 | snp | A/G | | | intron-variant | Asb9 | GRCm38.p3 | X:164516363 | TCCATTGGGGGCCCT[A/G]TGTTCCATCCAATAG | 69299 |
rs579096399 | snp | G/T | | | intron-variant | Asb9 | GRCm38.p3 | X:164518126 | ATCCTGCCAATCCAT[G/T]AACATGGGAGATCTT | 69299 |
rs579241241 | snp | C/T | | | intron-variant | Asb9 | GRCm38.p3 | X:164517378 | CTTGAGTTCTTTATA[C/T]ATATTGGATATTAGT | 69299 |
rs579265525 | snp | C/T | | | intron-variant | Asb9 | GRCm38.p3 | X:164523500 | TGGCATTCCCCTGTA[C/T]TGAGGCATATAAAGT | 69299 |
rs579275463 | snp | A/G | | | intron-variant | Asb9 | GRCm38.p3 | X:164528294 | GTCAGGAATTCAAAC[A/G]TTTTGTTAGGGCAGG | 69299 |
rs579321819 | snp | C/T | | | intron-variant | Asb9 | GRCm38.p3 | X:164532954 | CAGGCACTGGCATAG[C/T]CTCATATGAGACAGC | 69299 |
rs579322968 | snp | A/T | | | intron-variant | Asb9 | GRCm38.p3 | X:164516507 | TTTGGAGGCTGATTA[A/T]GGGATGGATCCCCGG | 69299 |
rs579331388 | snp | A/G | | | intron-variant | Asb9 | GRCm38.p3 | X:164518197 | CTTGAAGTTCTTATC[A/G]TACAGACCTTTCACT | 69299 |
rs579341735 | snp | G/T | | | upstream-variant-2KB | Asb9 | GRCm38.p3 | X:164496777 | TAGGGGAGTGGGGGT[G/T]GGTGGGTATGGGGGA | 69299 |
rs579453536 | snp | A/G | | | intron-variant | Asb9 | GRCm38.p3 | X:164507021 | TGTGTGTGTGTGTGT[A/G]TGTGTGTGTGTGTGT | 69299 |
rs579460589 | snp | A/G | | | intron-variant | Asb9 | GRCm38.p3 | X:164532688 | CTTCTTGGCCCTGGC[A/G]TTCCCCTGTACTGGG | 69299 |
rs579495680 | snp | A/C | | | intron-variant | Asb9 | GRCm38.p3 | X:164519012 | TAATTGTGGCTTCAT[A/C]GAATGAATTGCGTAG | 69299 |
rs579749131 | snp | A/C | | | intron-variant | Asb9 | GRCm38.p3 | X:164518480 | TTTCCAATTTGTATC[A/C]CATTGATCTCCTTTT | 69299 |
rs579785835 | snp | C/G | | | intron-variant | Asb9 | GRCm38.p3 | X:164537134 | TTTCTTTCTTTGTTT[C/G]TTTCTTTCTTTGTTT | 69299 |
rs579788726 | snp | C/T | | | intron-variant | Asb9 | GRCm38.p3 | X:164499099 | TCCAGGTTACTGTCC[C/T]GACTTTTTTTAATGA | 69299 |
rs579835863 | snp | A/T | | | intron-variant | Asb9 | GRCm38.p3 | X:164516553 | GATGGTCCATCCTTT[A/T]GTCCCAGCTCCAAAC | 69299 |
rs579842034 | snp | C/G | | | intron-variant | Asb9 | GRCm38.p3 | X:164523656 | TGCAGACCCCTTCAG[C/G]TCTTTGGGTACTTTC | 69299 |
rs579854721 | snp | C/T | | | intron-variant | Asb9 | GRCm38.p3 | X:164517562 | CTATTCAGTAATAGT[C/T]CCCCTGTGCCCACAT | 69299 |
rs579883742 | snp | A/G | | | intron-variant | Asb9 | GRCm38.p3 | X:164532308 | AGGAGAGAGAGAGAG[A/G]GAGAGAGAGAGAAGA | 69299 |
rs579887639 | snp | A/G | | | intron-variant | Asb9 | GRCm38.p3 | X:164510377 | TTGCAAGACCAAGGG[A/G]CCTCTCTTCCCAATG | 69299 |
rs579991716 | snp | C/T | | | intron-variant | Asb9 | GRCm38.p3 | X:164516886 | GTTTTCTGTAACCAT[C/T]CCTCTGTTGAGGGGC | 69299 |
rs580005748 | snp | C/T | | | intron-variant | Asb9 | GRCm38.p3 | X:164536034 | TCCCTGTGAAAGCCA[C/T]TCAACCTTCTAAGGG | 69299 |
rs580027978 | snp | C/T | | | intron-variant | Asb9 | GRCm38.p3 | X:164519132 | CATCTCGTCCTGCGC[C/T]TTTTTTTTGGTTGGG | 69299 |
rs580046547 | snp | A/T | | | intron-variant | Asb9 | GRCm38.p3 | X:164518302 | TTTCTCAGCCTGTTT[A/T]TCCTTTGTGTAGAGA | 69299 |
rs580064418 | snp | C/T | | | intron-variant | Asb9 | GRCm38.p3 | X:164524678 | TTCCTTTCCTTTCCT[C/T]TCCTTTCCTTTTCTC | 69299 |
rs580152517 | snp | A/G | | | upstream-variant-2KB | Asb9 | GRCm38.p3 | X:164497420 | GCTGTACGGTTTGAA[A/G]TAATTATTTGTAGTC | 69299 |
rs580323760 | snp | A/G | | | intron-variant | Asb9 | GRCm38.p3 | X:164517716 | TCCTATATGATAACC[A/G]CCATTTGTGCCAGCA | 69299 |
rs580375666 | snp | C/T | | | intron-variant | Asb9 | GRCm38.p3 | X:164532684 | CCCACTTCTTGGCCC[C/T]GGCATTCCCCTGTAC | 69299 |
rs580491237 | snp | A/G | | | intron-variant | Asb9 | GRCm38.p3 | X:164502807 | AACATGCACCCATGC[A/G]CACACACACACACAC | 69299 |
rs580497200 | snp | A/G | | | intron-variant | Asb9 | GRCm38.p3 | X:164518921 | TTATTGAGTATTTTT[A/G]CATTGATATTCATAA | 69299 |
rs580533456 | snp | A/G | | | intron-variant | Asb9 | GRCm38.p3 | X:164518398 | TAGGAGTTCTCTGGT[A/G]GAAATTTTAGGGTCA | 69299 |
rs580543759 | snp | A/G | | | intron-variant | Asb9 | GRCm38.p3 | X:164498482 | TCAGTAAATGTGGTT[A/G]AATCCTCAGGAACTG | 69299 |
rs580549029 | snp | A/T | | | intron-variant | Asb9 | GRCm38.p3 | X:164516258 | ATGCAACTAGAGACA[A/T]GAGCTCCAGGGGTAC | 69299 |
rs580594631 | snp | A/C | | | intron-variant | Asb9 | GRCm38.p3 | X:164519447 | GATTTTCTCAAAAAA[A/C]CAGCTCCTTGTTTGG | 69299 |
rs580605304 | snp | A/C/G | | | intron-variant | Asb9 | GRCm38.p3 | X:164518599 | TGGGATTTCTTCCAG[A/C/G]TTCTCACCATTTACT | 69299 |
rs580667810 | snp | C/T | | | intron-variant | Asb9 | GRCm38.p3 | X:164537071 | CTTCCTTCCTTCCTT[C/T]CTTCCTTCCTTCCTT | 69299 |
rs580715459 | snp | C/T | | | intron-variant | Asb9 | GRCm38.p3 | X:164517914 | TCTGAAGTACAGCTT[C/T]AGGTCAGGCATGGTG | 69299 |
rs581048683 | snp | C/T | | | intron-variant | Asb9 | GRCm38.p3 | X:164517143 | CTTTCTCCACATCCT[C/T]GACAGCATCTGCTGT | 69299 |
rs581052804 | snp | C/G | | | intron-variant | Asb9 | GRCm38.p3 | X:164525993 | GGGCCTCTCTTCCCA[C/G]TGATGACTGACTAGG | 69299 |
rs581067546 | snp | G/T | | | intron-variant | Asb9 | GRCm38.p3 | X:164532786 | ACATATGCAGCTAGA[G/T]ACACAAGCTCTGAGG | 69299 |
rs581105520 | snp | C/G | | | intron-variant | Asb9 | GRCm38.p3 | X:164537146 | TTTCTTTCTTTCTTT[C/G]TTTCTTTCTTTCTTT | 69299 |
rs581109038 | snp | A/G | | | intron-variant | Asb9 | GRCm38.p3 | X:164517172 | GTCACCTGAATTTTT[A/G]ATCTTAGCCATTCTG | 69299 |
rs581151610 | snp | A/C | | | intron-variant | Asb9 | GRCm38.p3 | X:164518079 | TGAATCTGTAGATTG[A/C]TTTTGGCAAGACAGC | 69299 |
rs581172766 | snp | C/T | | | intron-variant | Asb9 | GRCm38.p3 | X:164526142 | ATGGGGCTGCAAACC[C/T]CTTCAGCTCCTTGGA | 69299 |
rs581228184 | snp | C/T | | | intron-variant | Asb9 | GRCm38.p3 | X:164519545 | GCCATCTACTTCTCT[C/T]GGGTGAATTTTCTTC | 69299 |
rs581242434 | snp | C/G | | | intron-variant | Asb9 | GRCm38.p3 | X:164518518 | AATTGCTCTGGCTAG[C/G]ACATCAAGTACTATG | 69299 |
rs581260635 | snp | C/T | | | intron-variant | Asb9 | GRCm38.p3 | X:164499263 | ATATATACTAACAGT[C/T]TTAAAAATTTAGAAT | 69299 |
rs581289667 | snp | C/G | | | intron-variant | Asb9 | GRCm38.p3 | X:164518173 | TTCTTTAATTTCTTT[C/G]TACAGAGACTTGAAG | 69299 |
rs581376634 | snp | A/G | | | intron-variant | Asb9 | GRCm38.p3 | X:164532871 | TCCTTGGACACTTTC[A/G]CTGGCTCCTCCATTG | 69299 |
rs581581667 | snp | C/T | | | intron-variant | Asb9 | GRCm38.p3 | X:164519271 | ATTTCATCCCGGTTT[C/T]CCAGTTCTGTTGAGT | 69299 |
rs581594496 | snp | C/T | | | intron-variant | Asb9 | GRCm38.p3 | X:164516171 | GGCCCTGATGTTCCC[C/T]TGTACTGAGGCATAT | 69299 |
rs581630988 | snp | A/T | | | intron-variant | Asb9 | GRCm38.p3 | X:164525475 | TGTGTGTGTGTGTGT[A/T]GGGATAGTGAAAGGA | 69299 |
rs581651691 | snp | A/G | | | intron-variant | Asb9 | GRCm38.p3 | X:164516510 | GGAGGCTGATTATGG[A/G]ATGGATCCCCGGGTA | 69299 |
rs581745872 | snp | C/G | | | intron-variant | Asb9 | GRCm38.p3 | X:164517031 | TTGTGGGATCCTCCG[C/G]TAGTACTATGTCCAA | 69299 |
rs581786449 | snp | C/T | | | intron-variant | Asb9 | GRCm38.p3 | X:164499429 | TTTCCTAACCTAATA[C/T]ATATATATACACATA | 69299 |
rs581793433 | snp | A/G | | | intron-variant | Asb9 | GRCm38.p3 | X:164518547 | TGTTTAATAGGTAGG[A/G]AGAAAGTGGGCAGCC | 69299 |
rs581815798 | snp | G/T | | | intron-variant | Asb9 | GRCm38.p3 | X:164533991 | GTGTTTTGTTTGTTT[G/T]TTTTTTTTTCTTGAA | 69299 |
rs581826344 | snp | C/T | | | intron-variant | Asb9 | GRCm38.p3 | X:164518229 | CCTTAGTTAGAGTCA[C/T]GCCAAGGTGTTTTAT | 69299 |
rs581833418 | snp | C/T | | | intron-variant | Asb9 | GRCm38.p3 | X:164518607 | CTTCCAGCTTCTCAC[C/T]ATTTACTCTGATGTT | 69299 |
rs581834630 | snp | A/T | | | upstream-variant-2KB | Asb9 | GRCm38.p3 | X:164496902 | TATGCACAATGAATA[A/T]TTTTTCAGGGGAAAA | 69299 |
rs581892124 | snp | A/G | | | intron-variant | Asb9 | GRCm38.p3 | X:164523622 | TGGTTAGTTCATATT[A/G]TTGTTCCACCTATAG | 69299 |
rs581964413 | snp | A/G | | | intron-variant | Asb9 | GRCm38.p3 | X:164499550 | TATACATATATACAT[A/G]TATGGATAAATATAT | 69299 |
rs581997018 | snp | A/T | | | intron-variant | Asb9 | GRCm38.p3 | X:164530283 | AAGTATTGGAAAAAA[A/T]GGCCTCCATCTTGTG | 69299 |
rs582008327 | snp | A/T | | | intron-variant | Asb9 | GRCm38.p3 | X:164517531 | TCTTGATCTTACAGC[A/T]CAAGCCATTGATGTT | 69299 |
rs582163578 | snp | A/G | | | upstream-variant-2KB | Asb9 | GRCm38.p3 | X:164497124 | CCAGTCTGCAGAGGT[A/G]GAATTTCACAAGGTC | 69299 |
rs582290646 | snp | G/T | | | intron-variant | Asb9 | GRCm38.p3 | X:164518294 | CTAATTTCTTTCTCA[G/T]CCTGTTTTTCCTTTG | 69299 |
rs582393415 | snp | C/T | | | intron-variant | Asb9 | GRCm38.p3 | X:164523428 | TTCCTCTCTGAAAGT[C/T]CCCTATACCCTCCCC | 69299 |
rs582393978 | snp | A/T | | | intron-variant | Asb9 | GRCm38.p3 | X:164516311 | CACCTATAGGGTTGC[A/T]GACCCCTTTAGCTCC | 69299 |
rs582431324 | snp | A/C | | | intron-variant | Asb9 | GRCm38.p3 | X:164518745 | CTTTCTCGGCATCTA[A/C]TGAGATGATCATGTG | 69299 |
rs582438936 | snp | A/C | | | intron-variant | Asb9 | GRCm38.p3 | X:164499796 | GTGTGCACCACTCCA[A/C]CAAAGTATTATCTTT | 69299 |
rs582549531 | snp | A/C | | | intron-variant | Asb9 | GRCm38.p3 | X:164516383 | CCATCCAATAGCTGA[A/C]TATGAGCATCCACTT | 69299 |
rs582593789 | snp | C/T | | | intron-variant | Asb9 | GRCm38.p3 | X:164537027 | TTTTTTTCCTTTCTT[C/T]CTTCCTTCCTTCCTT | 69299 |
rs582604222 | snp | C/T | | | intron-variant | Asb9 | GRCm38.p3 | X:164518304 | TCTCAGCCTGTTTTT[C/T]CTTTGTGTAGAGAAA | 69299 |
rs582620671 | snp | C/T | | | intron-variant | Asb9 | GRCm38.p3 | X:164498408 | AAATATTTAAGTCTA[C/T]GGGTGTTTTGCCTAT | 69299 |
rs582718392 | snp | A/G | | | intron-variant | Asb9 | GRCm38.p3 | X:164502844 | ACACACACACACACA[A/G]ATGAGCACAATAGGG | 69299 |
rs582732872 | snp | C/G | | | intron-variant | Asb9 | GRCm38.p3 | X:164528384 | CTCACTGAGGCAGCA[C/G]CTGACAAGATCCCAT | 69299 |
rs582883085 | snp | C/T | | | intron-variant | Asb9 | GRCm38.p3 | X:164517382 | AGTTCTTTATATATA[C/T]TGGATATTAGTCCCC | 69299 |
rs582946568 | snp | C/G | | | intron-variant | Asb9 | GRCm38.p3 | X:164519023 | TCATAGAATGAATTG[C/G]GTAGAGTACCTTCTG | 69299 |
rs582967468 | snp | A/T | | | intron-variant | Asb9 | GRCm38.p3 | X:164518929 | TATTTTTGCATTGAT[A/T]TTCATAAGGGAAATA | 69299 |
rs583050134 | snp | G/T | | | intron-variant | Asb9 | GRCm38.p3 | X:164525954 | ATTCCCCTATACTGG[G/T]GCATAGAACCTTCAT | 69299 |
rs583116250 | snp | A/G | | | intron-variant | Asb9 | GRCm38.p3 | X:164517054 | ATGTCCAATTTTCTG[A/G]GGAACCACCAGACTG | 69299 |
rs583122887 | snp | A/T | | | intron-variant | Asb9 | GRCm38.p3 | X:164507779 | GTACACGCTCATGTG[A/T]GTGTGTGTACAGAAG | 69299 |
rs583128354 | snp | C/T | | | intron-variant | Asb9 | GRCm38.p3 | X:164537084 | TTCCTTCCTTCCTTC[C/T]TTTTTTCTTTTTCTT | 69299 |
rs583135464 | snp | C/T | | | intron-variant | Asb9 | GRCm38.p3 | X:164498488 | AATGTGGTTGAATCC[C/T]CAGGAACTGGGGTTA | 69299 |
rs583139785 | snp | A/G | | | intron-variant | Asb9 | GRCm38.p3 | X:164518410 | GGTAGAAATTTTAGG[A/G]TCACTTATATGTACT | 69299 |
rs583160728 | snp | A/T | | | intron-variant | Asb9 | GRCm38.p3 | X:164532719 | GCATATAAAGTTTGC[A/T]AGACCAAAGAGCCTC | 69299 |
rs583174081 | snp | C/T | | | intron-variant | Asb9 | GRCm38.p3 | X:164518048 | AATTGAGTTGGAATT[C/T]TAATGGGGGTTCCAT | 69299 |
rs583270050 | snp | G/T | | | intron-variant | Asb9 | GRCm38.p3 | X:164499123 | TTAATGATGAACAGT[G/T]ATGTGGAAGAGTAAG | 69299 |
rs583293168 | snp | A/C | | | intron-variant | Asb9 | GRCm38.p3 | X:164518482 | TCCAATTTGTATCAC[A/C]TTGATCTCCTTTTGT | 69299 |
rs583476622 | snp | C/T | | | intron-variant | Asb9 | GRCm38.p3 | X:164517615 | CTCCTGTATAAGTTT[C/T]ACTATCTCTGGTTTT | 69299 |
rs583495918 | snp | C/T | | | intron-variant | Asb9 | GRCm38.p3 | X:164524690 | CCTTTCCTTTCCTTT[C/T]CTCTGTCTGTCTGTC | 69299 |
rs583543300 | snp | A/G | | | intron-variant | Asb9 | GRCm38.p3 | X:164516744 | GTGAGTACATATCAT[A/G]TGAGTTTTTTTGTGA | 69299 |
rs583656097 | snp | C/T | | | intron-variant | Asb9 | GRCm38.p3 | X:164532649 | TACCCTCCCTGCCCC[C/T]ACTCCCCTACCCACC | 69299 |
rs583699159 | snp | G/T | | | intron-variant | Asb9 | GRCm38.p3 | X:164516955 | GCTGCTATGAACATA[G/T]TGGTGCATGTGTCCT | 69299 |
rs583734265 | snp | A/G | | | intron-variant | Asb9 | GRCm38.p3 | X:164510564 | ATCCAATAGCTGACT[A/G]TGAGCATCCACTTCT | 69299 |
rs583738292 | snp | C/G | | | intron-variant | Asb9 | GRCm38.p3 | X:164519149 | TTTTTTTGGTTGGGA[C/G]ACTATTAATGACTGC | 69299 |
rs583835417 | snp | A/G | | | intron-variant | Asb9 | GRCm38.p3 | X:164532685 | CCACTTCTTGGCCCT[A/G]GCATTCCCCTGTACT | 69299 |
rs584007659 | snp | A/C/T | | | intron-variant | Asb9 | GRCm38.p3 | X:164518573 | CAGCCTTGTCTAGTC[A/C/T]CTGATTTTAGTGGGA | 69299 |
rs584046683 | snp | C/T | | | intron-variant | Asb9 | GRCm38.p3 | X:164519456 | AAAAAACCAGCTCCT[C/T]GTTTGGTTGATTCTT | 69299 |
rs584115830 | snp | A/C | | | intron-variant | Asb9 | GRCm38.p3 | X:164517831 | TCATTTCTGGGTCTT[A/C]AATTCTATTCCATTG | 69299 |
rs584204603 | snp | A/G | | | intron-variant | Asb9 | GRCm38.p3 | X:164499434 | TAACCTAATACATAT[A/G]TATACACATATATAT | 69299 |
rs584230069 | snp | C/T | | | intron-variant | Asb9 | GRCm38.p3 | X:164499792 | AAAAGTGTGCACCAC[C/T]CCACCAAAGTATTAT | 69299 |
rs584264189 | snp | G/T | | | intron-variant | Asb9 | GRCm38.p3 | X:164516274 | GAGCTCCAGGGGTAC[G/T]GGTTAGTTCATATTG | 69299 |
rs584431485 | snp | C/T | | | intron-variant | Asb9 | GRCm38.p3 | X:164518672 | TTTAGGTATGGGCCT[C/T]GAATTCCTGATCTTT | 69299 |
rs584481910 | snp | A/G | | | intron-variant | Asb9 | GRCm38.p3 | X:164534330 | ATTTGTTGACCAGGC[A/G]ACTGGGCATTGTGTG | 69299 |
rs584494356 | snp | A/G | | | intron-variant | Asb9 | GRCm38.p3 | X:164518245 | GCCAAGGTGTTTTAT[A/G]TTATTTGTGACTATT | 69299 |
rs584533294 | snp | C/T | | | intron-variant | Asb9 | GRCm38.p3 | X:164526045 | GCTAGAGCCATGAGT[C/T]CCACCATGTGTTTTG | 69299 |
rs584545003 | snp | A/C | | | intron-variant | Asb9 | GRCm38.p3 | X:164517145 | TTCTCCACATCCTCG[A/C]CAGCATCTGCTGTCA | 69299 |
rs584572174 | snp | A/T | | | intron-variant | Asb9 | GRCm38.p3 | X:164518101 | CAAGACAGCCATTTT[A/T]ACTATATTTATCCTG | 69299 |
rs584733149 | snp | C/T | | | intron-variant | Asb9 | GRCm38.p3 | X:164528265 | AACAGACATGTGGGT[C/T]TGTTAACAACTCTGT | 69299 |
rs584795888 | snp | A/G | | | intron-variant | Asb9 | GRCm38.p3 | X:164532799 | GATACACAAGCTCTG[A/G]GGCTACTGGTTAGTT | 69299 |
rs584802135 | snp | A/C | | | intron-variant | Asb9 | GRCm38.p3 | X:164516228 | CTTTCCAATGATGGC[A/C]GACTTCTGATACATA | 69299 |
rs584846246 | snp | A/G | | | intron-variant | Asb9 | GRCm38.p3 | X:164517319 | TTTGTTTAGCTCTGA[A/G]CTCCATTTTTAATTG | 69299 |
rs584868518 | snp | A/T | | | intron-variant | Asb9 | GRCm38.p3 | X:164516337 | GCTCCTTGGGTACTT[A/T]CTCTAGCTCCTCCAT | 69299 |
rs584876639 | snp | A/G | | | intron-variant | Asb9 | GRCm38.p3 | X:164519589 | GCTTTTAGGTGTTTT[A/G]TCAAGCTGCTAGTGT | 69299 |
rs584925343 | snp | C/T | | | intron-variant | Asb9 | GRCm38.p3 | X:164534358 | GTGTGTGTGGAGTCC[C/T]TAGTTCAGGTAAAAA | 69299 |
rs584965789 | snp | A/T | | | intron-variant | Asb9 | GRCm38.p3 | X:164518521 | TGCTCTGGCTAGCAC[A/T]TCAAGTACTATGTTT | 69299 |
rs584975680 | snp | C/T | | | intron-variant | Asb9 | GRCm38.p3 | X:164499286 | TTTAGAATGTATGCA[C/T]AATGAATAATTTTTC | 69299 |
rs585046980 | snp | A/C | | | intron-variant | Asb9 | GRCm38.p3 | X:164519291 | TTCTGTTGAGTATAG[A/C]CTTTTGTAGAAGGAT | 69299 |
rs585144102 | snp | A/G | | | intron-variant | Asb9 | GRCm38.p3 | X:164532933 | AGCATCCACTTCTGT[A/G]TTTGCCAGGCACTGG | 69299 |
rs585155057 | snp | A/G | | | intron-variant | Asb9 | GRCm38.p3 | X:164518186 | TTGTACAGAGACTTG[A/G]AGTTCTTATCATACA | 69299 |
rs585267833 | snp | A/G | | | intron-variant | Asb9 | GRCm38.p3 | X:164523638 | TTGTTCCACCTATAG[A/G]GTTGCAGACCCCTTC | 69299 |
rs585281078 | snp | A/T | | | upstream-variant-2KB | Asb9 | GRCm38.p3 | X:164496973 | TTCATAATGCTAGGA[A/T]AGCATTGTATCACCA | 69299 |
rs585362767 | snp | A/G | | | intron-variant | Asb9 | GRCm38.p3 | X:164504068 | TTTTTTAATTGAGAT[A/G]TGTGTGTGTGTGTGT | 69299 |
rs585496935 | snp | A/G | | | intron-variant | Asb9 | GRCm38.p3 | X:164517410 | CCCTATCTGATTTAG[A/G]ATTGGTAAAGATACT | 69299 |
rs585504081 | snp | A/G | | | intron-variant | Asb9 | GRCm38.p3 | X:164528611 | AAGCAAATATTGACA[A/G]GAATAAGGCTGGGGG | 69299 |
rs585630579 | snp | A/C | | | intron-variant | Asb9 | GRCm38.p3 | X:164518295 | TAATTTCTTTCTCAG[A/C]CTGTTTTTCCTTTGT | 69299 |
rs585701932 | snp | C/T | | | intron-variant | Asb9 | GRCm38.p3 | X:164516520 | TATGGGATGGATCCC[C/T]GGGTATGGCAGTCTC | 69299 |
rs585734556 | snp | A/G | | | intron-variant | Asb9 | GRCm38.p3 | X:164531343 | GATTCAAGACCCCGA[A/G]AGAGGGCAGGGAAGA | 69299 |
rs585748521 | snp | G/T | | | intron-variant | Asb9 | GRCm38.p3 | X:164517555 | TGATGTTCTATTCAG[G/T]AATAGTTCCCCTGTG | 69299 |
rs585809520 | snp | A/G | | | intron-variant | Asb9 | GRCm38.p3 | X:164532650 | ACCCTCCCTGCCCCC[A/G]CTCCCCTACCCACCC | 69299 |
rs585879139 | snp | A/G | | | intron-variant | Asb9 | GRCm38.p3 | X:164516495 | ATGGTGTCAGCTTTT[A/G]GAGGCTGATTATGGG | 69299 |
rs585916393 | snp | A/G | | | intron-variant | Asb9 | GRCm38.p3 | X:164523922 | CAAGAACTGATACAC[A/G]GGCAACAGAGGAAGG | 69299 |
rs585928661 | snp | C/T | | | intron-variant | Asb9 | GRCm38.p3 | X:164516752 | ATATCATGTGAGTTT[C/T]TTTGTGATTGGGTTA | 69299 |
rs585970630 | snp | C/T | | | upstream-variant-2KB | Asb9 | GRCm38.p3 | X:164497238 | CCCAAATGGTCAGCC[C/T]TAAACACATGTACTT | 69299 |
rs586038616 | snp | G/T | | | intron-variant | Asb9 | GRCm38.p3 | X:164519002 | GGCATCAGAGTAATT[G/T]TGGCTTCATAGAATG | 69299 |
rs586161581 | snp | G/T | | | intron-variant | Asb9 | GRCm38.p3 | X:164517681 | AGTACAAGGAGATAG[G/T]AATGGATCAATTCAC | 69299 |
rs586213701 | snp | A/C | | | intron-variant | Asb9 | GRCm38.p3 | X:164523466 | GCTCCCCTACCCACC[A/C]ACTCCCACTTCTTGG | 69299 |
rs586218862 | snp | C/T | | | intron-variant | Asb9 | GRCm38.p3 | X:164502042 | TCTTTTTTTAAAGTC[C/T]AGTTCCATGGTTACA | 69299 |
rs586221081 | snp | C/T | | | intron-variant | Asb9 | GRCm38.p3 | X:164518894 | TGTTTTTGGATTCGA[C/T]TAGTGAGAATTTTAT | 69299 |
rs586243901 | snp | C/T | | | intron-variant | Asb9 | GRCm38.p3 | X:164537067 | CTTCCTTCCTTCCTT[C/T]CTTCCTTCCTTCCTT | 69299 |
rs586258045 | snp | A/G | | | intron-variant | Asb9 | GRCm38.p3 | X:164518388 | TTATCAGGTTTAGGA[A/G]TTCTCTGGTAGAAAT | 69299 |
rs586265736 | snp | G/T | | | intron-variant | Asb9 | GRCm38.p3 | X:164498462 | GTGCCTAGTTCTCCT[G/T]GAGATCAGTAAATGT | 69299 |
rs586367241 | snp | C/T | | | intron-variant | Asb9 | GRCm38.p3 | X:164498748 | TTCTTAAGGACTCTT[C/T]GACTTTCTCTCTTTT | 69299 |
rs586417523 | snp | A/G | | | intron-variant | Asb9 | GRCm38.p3 | X:164518050 | TTGAGTTGGAATTTT[A/G]ATGGGGGTTCCATTG | 69299 |
rs586597270 | snp | C/T | | | intron-variant | Asb9 | GRCm38.p3 | X:164518501 | ATCTCCTTTTGTTGT[C/T]GAATTGCTCTGGCTA | 69299 |
rs586734138 | snp | A/G | | | intron-variant | Asb9 | GRCm38.p3 | X:164517070 | GGAACCACCAGACTG[A/G]TTCTAAAAGAGTGGC | 69299 |
rs586741909 | snp | A/T | | | intron-variant | Asb9 | GRCm38.p3 | X:164525962 | ATACTGGGGCATAGA[A/T]CCTTCATAGGACCAA | 69299 |
rs586747244 | snp | C/G | | | intron-variant | Asb9 | GRCm38.p3 | X:164537130 | TTTCTTTCTTTCTTT[C/G]TTTCTTTCTTTCTTT | 69299 |
rs586761875 | snp | A/C | | | intron-variant | Asb9 | GRCm38.p3 | X:164518479 | CTTTCCAATTTGTAT[A/C]ACATTGATCTCCTTT | 69299 |
rs586804026 | snp | C/T | | | intron-variant | Asb9 | GRCm38.p3 | X:164519105 | AGGTCTGATAGAACT[C/T]TGTACTAAATCCATC | 69299 |
rs586904774 | snp | C/T | | | intron-variant | Asb9 | GRCm38.p3 | X:164532864 | CTTTAGCTCCTTGGA[C/T]ACTTTCACTGGCTCC | 69299 |
rs586936106 | snp | A/G | | | intron-variant | Asb9 | GRCm38.p3 | X:164532729 | TTTGCAAGACCAAAG[A/G]GCCTCTCTTCCCAAT | 69299 |
rs586943512 | snp | C/T | | | intron-variant | Asb9 | GRCm38.p3 | X:164509938 | CAAAATTGAGTCTAC[C/T]GAATTAGAAAAAAAA | 69299 |
rs586973728 | snp | A/C | | | intron-variant | Asb9 | GRCm38.p3 | X:164517026 | AGGTATTGTGGGATC[A/C]TCCGGTAGTACTATG | 69299 |
rs587003712 | snp | A/C | | | intron-variant | Asb9 | GRCm38.p3 | X:164499176 | AAGTTGCTTTTGATC[A/C]TGATGTTTTTATCAT | 69299 |
rs587149081 | snp | C/G | | | intron-variant | Asb9 | GRCm38.p3 | X:164519378 | TATTTTGTTAACTAG[C/G]ATGCTGTCCCTGTGC | 69299 |
rs587357941 | snp | C/T | | | intron-variant | Asb9 | GRCm38.p3 | X:164525432 | AAAGCATAGTTTGTG[C/T]GTGTGTGTGTGTGTG | 69299 |
rs587415670 | snp | G/T | | | intron-variant | Asb9 | GRCm38.p3 | X:164511769 | ATACTCCAGTGCCCT[G/T]AGATTTGCTGAAGCA | 69299 |
rs587420254 | snp | C/T | | | intron-variant | Asb9 | GRCm38.p3 | X:164519265 | TTGTCCATTTCATCC[C/T]GGTTTTCCAGTTCTG | 69299 |
rs587453571 | snp | A/G | | | intron-variant | Asb9 | GRCm38.p3 | X:164499425 | ATATTTTCCTAACCT[A/G]ATACATATATATACA | 69299 |
rs587462535 | snp | C/T | | | intron-variant | Asb9 | GRCm38.p3 | X:164532687 | ACTTCTTGGCCCTGG[C/T]ATTCCCCTGTACTGG | 69299 |
rs587471608 | snp | C/T | | | intron-variant | Asb9 | GRCm38.p3 | X:164517834 | TTTCTGGGTCTTCAA[C/T]TCTATTCCATTGGTC | 69299 |
rs587504936 | snp | A/T | | | intron-variant | Asb9 | GRCm38.p3 | X:164516255 | CATATGCAACTAGAG[A/T]CATGAGCTCCAGGGG | 69299 |
rs587548752 | snp | C/T | | | intron-variant | Asb9 | GRCm38.p3 | X:164518523 | CTCTGGCTAGCACAT[C/T]AAGTACTATGTTTAA | 69299 |