SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs3674523 | snp | C/G | 0.408163 | 0.193609 | intron-variant | Cd2ap | Mm_Celera | 17:42846906 | GGTAGGAGGATAGCA[C/G]GGATTTCTCCTACTT | 12488 |
rs3685040 | snp | A/T | 0.5 | 0 | intron-variant | Cd2ap | Mm_Celera | 17:42851439 | AATAATTTATTTTTT[A/T]AAATAATTTTTTAAA | 12488 |
rs3685544 | snp | C/G | 0.5 | 0 | intron-variant | Cd2ap | Mm_Celera | 17:42851492 | ATCTACATCTTTTCT[C/G]AATTACTTGACTAAG | 12488 |
rs3685750 | snp | A/G | 0.290657 | 0.246672 | intron-variant | Cd2ap | GRCm38.p3 | 17:42751821 | ATTTATACAGCTGGC[A/G]TGTCAGTGAAAGTCA | 12488 |
rs3686200 | snp | A/C | 0.5 | 0 | intron-variant | Cd2ap | Mm_Celera | 17:42851622 | AAAATTTGAATTACT[A/C]GGAAAACAAATACTA | 12488 |
rs3686273 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Cd2ap | Mm_Celera | 17:42851651 | TAAGCATGCATTCTA[C/T]AAAATACTACTGTGC | 12488 |
rs3688993 | snp | A/G | 0.5 | 0 | upstream-variant-2KB | Cd2ap | GRCm38.p3 | 17:42877297 | ATGAAGGCCGGCGTA[A/G]GATTATTGTAATCAA | 12488 |
rs3689060 | snp | A/C | 0.5 | 0 | upstream-variant-2KB | Cd2ap | GRCm38.p3 | 17:42877327 | AACACGAGCTTTCTT[A/C]AACTTATTGACAAAT | 12488 |
rs3689094 | snp | A/T | 0.5 | 0 | upstream-variant-2KB | Cd2ap | GRCm38.p3 | 17:42877352 | ACAAATTTAATTAAT[A/T]TGACCTTAATTTTCC | 12488 |
rs3695689 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Cd2ap | Mm_Celera | 17:42848026 | ACAAACAATAGGTTT[C/T]TCTGATTTTAAGTCA | 12488 |
rs3704191 | snp | C/G | 0.5 | 0 | upstream-variant-2KB | Cd2ap | GRCm38.p3 | 17:42877514 | ATTCTCACAGCTACC[C/G]GACACTTAAACTGCT | 12488 |
rs3704806 | snp | A/C | 0.5 | 0 | upstream-variant-2KB | Cd2ap | GRCm38.p3 | 17:42877616 | GGGTGAATGAACCTG[A/C]CTGGAGCTTTAGCAG | 12488 |
rs3704867 | snp | C/G | 0.5 | 0 | upstream-variant-2KB | Cd2ap | GRCm38.p3 | 17:42877651 | TGTGTTAAAAGAAAT[C/G]TTTATTTACAGTGTA | 12488 |
rs3704912 | snp | A/T | 0.5 | 0 | upstream-variant-2KB | Cd2ap | GRCm38.p3 | 17:42877677 | GTGTAGAACAAGAGT[A/T]GAGACTTTGTAAATA | 12488 |
rs3708927 | snp | A/G | 0.290657 | 0.246672 | intron-variant | Cd2ap | GRCm38.p3 | 17:42790296 | CGGTGTGTGTTGTGT[A/G]TGTTCATAGGCTATG | 12488 |
rs4136050 | snp | A/G | 0.290657 | 0.246672 | intron-variant | Cd2ap | GRCm38.p3 | 17:42790352 | GGAATATTGGAAGTA[A/G]TGTGACCAGATCTGT | 12488 |
rs6243792 | snp | A/G | 0.5 | 0 | intron-variant | Cd2ap | GRCm38.p3 | 17:42785490 | caacttttggatcag[A/G]atataagctctcagc | 12488 |
rs6244502 | snp | A/G | 0.5 | 0 | intron-variant | Cd2ap | GRCm38.p3 | 17:42785662 | tgaaatagaaaaata[A/G]ctaagataGCATCCA | 12488 |
rs6259068 | snp | C/T | 0.5 | 0 | intron-variant | Cd2ap | Mm_Celera | 17:42824890 | ACAACTCCCAGATCA[C/T]TGAGTTTGAGGCCAG | 12488 |
rs6259635 | snp | A/G | 0.5 | 0 | intron-variant | Cd2ap | Mm_Celera | 17:42825012 | ACAGAATTATAGAAA[A/G]NGTAAATATTTATTA | 12488 |
rs6259636 | snp | A/G | 0.5 | 0 | intron-variant | Cd2ap | Mm_Celera | 17:42825013 | CAGAATTATAGAAAN[A/G]GTAAATATTTATTAT | 12488 |
rs6272982 | snp | A/C | 0.244898 | 0.249948 | intron-variant | Cd2ap | Mm_Celera | 17:42831723 | AGTACCATGTTGTTT[A/C]TTGTCACAAATATTT | 12488 |
rs6273036 | snp | A/T | 0.5 | 0 | intron-variant | Cd2ap | Mm_Celera | 17:42831751 | TTTGTAATGTGTCAA[A/T]CTATATTAACNTTGA | 12488 |
rs6273059 | snp | A/G | 0.5 | 0 | intron-variant | Cd2ap | Mm_Celera | 17:42831762 | TCAANCTATATTAAC[A/G]TTGACCTATTTAATA | 12488 |
rs6273586 | snp | C/T | 0.5 | 0 | intron-variant | Cd2ap | Mm_Celera | 17:42831838 | GGGAAGTTGctttct[C/T]attaatcactgaatc | 12488 |
rs6273648 | snp | C/G | 0.5 | 0 | intron-variant | Cd2ap | Mm_Celera | 17:42831873 | gagtctggcacagtA[C/G]AAGCACTCAATATAC | 12488 |
rs6308576 | snp | C/T | 0.5 | 0 | intron-variant | Cd2ap | Mm_Celera | 17:42873577 | ACAAACAAAAAAAGA[C/T]TTATTTTTATTTAGT | 12488 |
rs6321139 | snp | A/G | 0.5 | 0 | intron-variant | Cd2ap | GRCm38.p3 | 17:42873603 | TTAGTGACAAATTAG[A/G]TAAAACATGAGTATT | 12488 |
rs6322392 | snp | C/T | 0.5 | 0 | intron-variant | Cd2ap | Mm_Celera | 17:42873867 | GGACAGTAAGgccta[C/T]aatcccagcagccaa | 12488 |
rs6323412 | snp | A/T | 0.5 | 0 | intron-variant | Cd2ap | Mm_Celera | 17:42874032 | AACTTGAATTTGAGG[A/T]TTTTAATGAATACAC | 12488 |
rs6351867 | snp | A/G | 0.5 | 0 | intron-variant | Cd2ap | Mm_Celera | 17:42803625 | aagatcaggttcaag[A/G]tcataactaatccaa | 12488 |
rs6365210 | snp | A/C | 0.5 | 0 | intron-variant | Cd2ap | Mm_Celera | 17:42803851 | TATCAAATAACAAAT[A/C]CTGTAATCATAATAT | 12488 |
rs6366281 | snp | G/T | 0.297521 | 0.245442 | intron-variant | Cd2ap | Mm_Celera | 17:42804043 | CTAAATAAAAACTTT[G/T]TTCCCAAGTGTTATT | 12488 |
rs6367333 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Cd2ap | GRCm38.p3 | 17:42804216 | CCACTTCTTTTTTAA[C/T]AGAATCCTAAGATTG | 12488 |
rs6367444 | snp | A/G | 0.5 | 0 | intron-variant | Cd2ap | Mm_Celera | 17:42804274 | TTAAACTCAGGGTCT[A/G]GGCATGAATTTTTTA | 12488 |
rs6368423 | snp | C/G | 0.391111 | 0.206368 | intron-variant | Cd2ap | Mm_Celera | 17:42804380 | TTAGTTAGACGAGCT[C/G]ATCTTTCATCTGATT | 12488 |
rs6370095 | snp | C/T | 0.5 | 0 | intron-variant | Cd2ap | Mm_Celera | 17:42831605 | TTGAAAAGCCTATGT[C/T]TTTCCTTCACTCTTA | 12488 |
rs6370548 | snp | A/G | 0.5 | 0 | intron-variant | Cd2ap | Mm_Celera | 17:42831667 | GCCTCAATAACATAA[A/G]TGACTTCTTCAAAAA | 12488 |
rs6398219 | snp | C/G | 0.5 | 0 | intron-variant | Cd2ap | GRCm38.p3 | 17:42773204 | tctaagagggaaact[C/G]atagctctgagtgcc | 12488 |
rs13461535 | snp | A/C | | | utr-variant-3-prime, intron-variant | Cd2ap | GRCm38.p3 | 17:42794951 | ATCATGCTTAAAAAA[A/C]CAATACATTTTCTTT | 12488 |
rs13461536 | snp | A/G | 0.444444 | 0.157135 | utr-variant-3-prime, intron-variant | Cd2ap | GRCm38.p3 | 17:42793589 | TAGTTCAGATTTGCT[A/G]GTCTTTGAAACACAG | 12488 |
rs13461537 | snp | A/G | 0.375 | 0.216506 | utr-variant-3-prime, intron-variant | Cd2ap | GRCm38.p3 | 17:42794394 | GAAAGGTCTAATAAC[A/G]GTAAAAAGTAACATA | 12488 |
rs13461538 | snp | A/T | | | utr-variant-3-prime, intron-variant | Cd2ap | Mm_Celera | 17:42794443 | CTCCTGCATTCCCAA[A/T]GGGAGGTTTGTCTCC | 12488 |
rs13461540 | snp | A/T | 0.375 | 0.216506 | utr-variant-3-prime, intron-variant | Cd2ap | Mm_Celera | 17:42794656 | ATGACAGGCATGCCC[A/T]GTGTGCCTAGCCTTT | 12488 |
rs13461541 | snp | C/T | 0.124444 | 0.216185 | utr-variant-3-prime, intron-variant | Cd2ap | GRCm38.p3 | 17:42795533 | TTTGTGCCTAGACAC[C/T]GCAGCACATGTGGAA | 12488 |
rs29497715 | snp | C/T | 0.375 | 0.216506 | upstream-variant-2KB | Cd2ap | Mm_Celera | 17:42878241 | CATGTATGTGTTCCA[C/T]ATGTCGGTGTACCAC | 12488 |
rs29497929 | snp | C/T | 0.32 | 0.24 | intron-variant | Cd2ap | Mm_Celera | 17:42859665 | GACTATGTGCTATTT[C/T]TTGTCCTAAGTATTT | 12488 |
rs29498331 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Cd2ap | Mm_Celera | 17:42861751 | ATGACTTATAATATC[A/C]ATGCACAACTTGTAG | 12488 |
rs29501409 | snp | C/T | 0.375 | 0.216506 | intron-variant | Cd2ap | GRCm38.p3 | 17:42825405 | TGTGATCACTGGTCA[C/T]TTCTTTTTCTTTTTC | 12488 |
rs29504504 | snp | C/G | 0.32 | 0.24 | intron-variant | Cd2ap | Mm_Celera | 17:42751358 | TTAATTATAGAGCCC[C/G]CAGGGGCATGAAAAG | 12488 |
rs29505975 | snp | A/C | 0.375 | 0.216506 | intron-variant | Cd2ap | Mm_Celera | 17:42866040 | TCTGCTGGAGACCTA[A/C]ATAAGGACATTGGAA | 12488 |
rs29515563 | snp | G/T | 0.375 | 0.216506 | intron-variant | Cd2ap | Mm_Celera | 17:42841385 | AAATTACTCTTCTGT[G/T]GGTTTGAAAATTCCC | 12488 |
rs29516189 | snp | A/G | 0.33241 | 0.236027 | intron-variant | Cd2ap | Mm_Celera | 17:42816973 | GTTAAAAACCAACAA[A/G]AAGGCAGCAAACACT | 12488 |
rs29516449 | snp | C/T | 0.375 | 0.216506 | upstream-variant-2KB | Cd2ap | Mm_Celera | 17:42878251 | TTCCATATGTCGGTG[C/T]ACCACATGCTTGCCT | 12488 |
rs29517465 | snp | A/C | 0.32 | 0.24 | intron-variant | Cd2ap | Mm_Celera | 17:42855085 | AATGAGAACCTCACT[A/C]TCAGTTACAATATTT | 12488 |
rs29518358 | snp | A/C | 0.375 | 0.216506 | intron-variant | Cd2ap | GRCm38.p3 | 17:42827423 | TATTAACTATACTCT[A/C]GTATTCACATTATGA | 12488 |
rs29518407 | snp | G/T | 0.32 | 0.24 | intron-variant | Cd2ap | Mm_Celera | 17:42859605 | GCATTGAGCAATCAT[G/T]AAAGTTTACAAGTCC | 12488 |
rs29520465 | snp | A/G | 0.375 | 0.216506 | intron-variant | Cd2ap | Mm_Celera | 17:42819588 | GTGGTCCACCCAACA[A/G]AATGTACAACATATA | 12488 |
rs29520854 | snp | A/C | 0.375 | 0.216506 | intron-variant | Cd2ap | Mm_Celera | 17:42873098 | CAATTTATATATTAA[A/C]ACAAAATCATCTTAC | 12488 |
rs29520926 | snp | A/G | 0.375 | 0.216506 | intron-variant | Cd2ap | Mm_Celera | 17:42845722 | ATAGCTCATTTCTAA[A/G]CTTGTACATTGTGCT | 12488 |
rs29521472 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Cd2ap | Mm_Celera | 17:42778237 | TCAGGAGAGAGAACT[C/G]GTCCCCAAGTGTTAC | 12488 |
rs29521868 | snp | G/T | 0.255 | 0.24995 | intron-variant | Cd2ap | Mm_Celera | 17:42834761 | AAATCTCAAACCAGT[G/T]GAATGATTCATCAGG | 12488 |
rs29522120 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Cd2ap | Mm_Celera | 17:42814528 | AATTTTAACAAATGA[A/G]ATACAAAGAGTATAT | 12488 |
rs29522522 | snp | A/T | 0.375 | 0.216506 | intron-variant | Cd2ap | Mm_Celera | 17:42863604 | GCCAGCCTGGTCTAC[A/T]GTGTGAGTTCCAGGA | 12488 |
rs29523797 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Cd2ap | Mm_Celera | 17:42866922 | AATTAGTATACCACT[A/G]GATTGAATTGGATTG | 12488 |
rs29523944 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Cd2ap | Mm_Celera | 17:42853261 | AAGGACCTGAACCAT[C/T]ACATGAGTTTACAAA | 12488 |
rs29523974 | snp | A/G | 0.391111 | 0.206368 | intron-variant, downstream-variant-500B | Cd2ap | Mm_Celera | 17:42808364 | CACTGAAGTAGATTT[A/G]CATTCCAAACAACAA | 12488 |
rs29523984 | snp | A/G | 0.444444 | 0.157135 | upstream-variant-2KB | Cd2ap | Mm_Celera | 17:42877962 | CCAAGCAAAGAACAC[A/G]AATAAAAAATTCATA | 12488 |
rs29524817 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Cd2ap | Mm_Celera | 17:42867172 | AAAAAAAAAAAAAAA[A/G]AAAGAAAAGAAAAGA | 12488 |
rs29530512 | snp | C/G | 0.569444 | 0.111976 | intron-variant | Cd2ap | GRCm38.p3 | 17:42789304 | GGATGAGGGGAAGAA[C/G]TATGTGAGGGTGGAC | 12488 |
rs29534211 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Cd2ap | Mm_Celera | 17:42812966 | TACAGCAGTTGTGAG[C/T]TGTCCATGTGGGTGC | 12488 |
rs29534868 | snp | C/T | 0.21875 | 0.248039 | intron-variant | Cd2ap | Mm_Celera | 17:42803300 | CTGACTAGTATTGAT[C/T]CCTGTGCAATCATTC | 12488 |
rs29538709 | snp | C/T | 0.375 | 0.216506 | intron-variant, upstream-variant-2KB | Cd2ap | Mm_Celera | 17:42829435 | TTACACTGATATAAA[C/T]AAAGGCCTTATGGCT | 12488 |
rs29539035 | snp | A/T | 0.375 | 0.216506 | intron-variant | Cd2ap | Mm_Celera | 17:42862804 | CTGACATATAATACA[A/T]AGCAATAGCTACATG | 12488 |
rs29540335 | snp | C/T | 0.375 | 0.216506 | intron-variant | Cd2ap | Mm_Celera | 17:42791121 | TGTCAATCAGGTCAC[C/T]TCAGTGGGATCCAAT | 12488 |
rs33042352 | snp | C/T | 0.32 | 0.24 | intron-variant | Cd2ap | Mm_Celera | 17:42859252 | ACAAATTTACACACA[C/T]ACTCATTCCCCCACC | 12488 |
rs33046320 | snp | C/T | 0.375 | 0.216506 | intron-variant | Cd2ap | Mm_Celera | 17:42865761 | GTACCAGAAGTGGGG[C/T]GGATTGTAATGGCTA | 12488 |
rs33052379 | snp | C/T | 0.265928 | 0.249492 | intron-variant | Cd2ap | Mm_Celera | 17:42818096 | GACCTCCACATCTAA[C/T]TTAAATGGCAGGACT | 12488 |
rs33055802 | snp | A/T | 0.375 | 0.216506 | intron-variant | Cd2ap | Mm_Celera | 17:42844909 | AAAATTAAAAAAAAA[A/T]TAAATAAAAAAACAA | 12488 |
rs33057300 | snp | G/T | 0.32 | 0.24 | intron-variant | Cd2ap | Mm_Celera | 17:42779637 | ACAACTCTAATCCCA[G/T]TACTTGGGAGGCAGA | 12488 |
rs33067797 | snp | C/T | 0.375 | 0.216506 | intron-variant | Cd2ap | Mm_Celera | 17:42873264 | CTCCTCACCAATTTA[C/T]AGACCAATAAACTGA | 12488 |
rs33067825 | snp | C/T | 0.375 | 0.216506 | utr-variant-3-prime, intron-variant | Cd2ap | GRCm38.p3 | 17:42794274 | TAACACATAAACTCA[C/T]TTTTCTGTTAGTTAT | 12488 |
rs33073335 | snp | A/G | 0.375 | 0.216506 | intron-variant, downstream-variant-500B | Gpr111, Cd2ap | Mm_Celera | 17:42748608 | AACTCCCAGCATGCC[A/G]GGAAGTTATATGGTC | 12488 |
rs33075171 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Cd2ap | Mm_Celera | 17:42874199 | AGAAACGGCGTGTGG[A/C]CAGTAAATACAGGTA | 12488 |
rs33095827 | snp | G/T | 0.375 | 0.216506 | intron-variant | Cd2ap | Mm_Celera | 17:42855419 | CCTCAAACAATGACG[G/T]CTTCCAAATTTACAG | 12488 |
rs33102734 | snp | C/T | 0.375 | 0.216506 | intron-variant | Cd2ap | Mm_Celera | 17:42871041 | CTTTGAAAGAAAACT[C/T]TTCTTTGTGTTCGGA | 12488 |
rs33103835 | snp | A/G | 0.375 | 0.216506 | intron-variant | Cd2ap | Mm_Celera | 17:42838908 | ATAAAGAGGAAAAAA[A/G]CAAATGATTTAAACA | 12488 |
rs33111986 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Cd2ap | GRCm38.p3 | 17:42814269 | TTAAGACTTTTGTGA[A/T]AAAGATCACAAAAAT | 12488 |
rs33117278 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Cd2ap | Mm_Celera | 17:42840482 | TTTCCAATTCCAATA[C/T]TAAGCATCGGTTATG | 12488 |
rs33117546 | snp | A/G | 0.375 | 0.216506 | intron-variant, upstream-variant-2KB | Cd2ap | GRCm38.p3 | 17:42829337 | TCACTTTTTAAAATA[A/G]CGCAATTTTAGGTAT | 12488 |
rs33122914 | snp | A/C | 0.375 | 0.216506 | intron-variant | Cd2ap | Mm_Celera | 17:42783077 | TCTGGACTCCCCCTT[A/C]TGTCTCCCTTCCTAT | 12488 |
rs33124655 | snp | A/G | 0.32 | 0.24 | intron-variant | Cd2ap | Mm_Celera | 17:42780504 | GGATTTCTACTTTGT[A/G]CAAACAAAACAAAAC | 12488 |
rs33126775 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Cd2ap | Mm_Celera | 17:42871578 | AACCCTCAAGTTTTT[C/T]TGGAAAAACAAAGTC | 12488 |
rs33129665 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Cd2ap | Mm_Celera | 17:42839879 | TCAAGTAATGTTATT[A/G]TAACTTAAGTCATTG | 12488 |
rs33131249 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Cd2ap | Mm_Celera | 17:42812903 | GTAGGTTATGCCCAC[A/G]TGAATAGAAGCACTC | 12488 |
rs33138215 | snp | A/G | 0.375 | 0.216506 | intron-variant | Cd2ap | GRCm38.p3 | 17:42785079 | AATGGGCATGTTGAT[A/G]TGGGAGGGGGAAATT | 12488 |
rs33140171 | snp | A/G | 0.375 | 0.216506 | intron-variant | Cd2ap | Mm_Celera | 17:42865988 | CAAGTCCCAGATCCA[A/G]GAGTGGTGGTAAACA | 12488 |
rs33141922 | snp | C/T | 0.375 | 0.216506 | intron-variant | Cd2ap | Mm_Celera | 17:42786790 | TACTGGGTTTTTTTT[C/T]CCCCTAAAGTGTTTG | 12488 |
rs33146425 | snp | A/T | 0.32 | 0.24 | intron-variant | Cd2ap | Mm_Celera | 17:42779744 | AATAAATAAATAAAT[A/T]AGATTAGATTAGATT | 12488 |
rs33149775 | snp | A/T | 0.375 | 0.216506 | intron-variant | Cd2ap | Mm_Celera | 17:42840970 | CTAATTCCAGTTTTG[A/T]CTGTACTTCATGCAT | 12488 |
rs33153563 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Cd2ap | Mm_Celera | 17:42872009 | ACTGGTAAAATGGTT[C/T]AAGAGGCAACGAGCA | 12488 |
rs33153704 | snp | C/T | 0.484429 | 0.0868505 | intron-variant | Cd2ap | Mm_Celera | 17:42798481 | TTAGGCAACTATTAC[C/T]ATAAAATGGGGTAGC | 12488 |
rs33153739 | snp | C/T | 0.375 | 0.216506 | intron-variant | Cd2ap | Mm_Celera | 17:42866394 | GATGGTTGTGAGCCA[C/T]CATGTGGTTGCTGGG | 12488 |
rs33154030 | snp | A/G | 0.290657 | 0.246672 | intron-variant, downstream-variant-500B | Cd2ap | Mm_Celera | 17:42808435 | ATACTATGGAAGAAG[A/G]AATTACCAAGAGGTG | 12488 |
rs33154832 | snp | A/T | 0.465374 | 0.126941 | intron-variant | Cd2ap | GRCm38.p3 | 17:42825265 | CCTTGGACTTTCACA[A/T]GCATGGCGTGTGTAC | 12488 |
rs33157783 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Cd2ap | Mm_Celera | 17:42840681 | ATTTAGGACCACCTG[C/T]CACTGTTTCTCAAAC | 12488 |
rs33160992 | snp | A/G | 0.375 | 0.216506 | intron-variant | Cd2ap | Mm_Celera | 17:42858204 | TAATCCCAGCACTCA[A/G]AAGGCAGAGGCAGGT | 12488 |
rs33161930 | snp | C/G | 0.375 | 0.216506 | upstream-variant-2KB | Cd2ap | Mm_Celera | 17:42878184 | AGCTAGGAGTGTCTT[C/G]CAAAGATAAAACCAT | 12488 |
rs33162622 | snp | A/G | 0.375 | 0.216506 | intron-variant | Cd2ap | Mm_Celera | 17:42864644 | AACCATGGGTCTCAT[A/G]TATCTTGTGAACTGA | 12488 |
rs33165484 | snp | C/T | 0.297521 | 0.245442 | intron-variant | Cd2ap | Mm_Celera | 17:42840182 | TCAGTCTTTACCATA[C/T]CTTGTACAATCACAC | 12488 |
rs33166339 | snp | A/C | 0.375 | 0.216506 | intron-variant | Cd2ap | Mm_Celera | 17:42818474 | GAGAGAATCAACTTA[A/C]ACAAGTTGTCCTCCA | 12488 |
rs33173292 | snp | C/T | 0.475309 | 0.108333 | intron-variant | Cd2ap | Mm_Celera | 17:42756976 | CTGCTCTAGTCTAAA[C/T]GGGAGTTACAAGCAA | 12488 |
rs33174067 | snp | A/G | 0.33241 | 0.236027 | intron-variant | Cd2ap | Mm_Celera | 17:42834541 | TGAGGACTTACAACC[A/G]ATTACATCCTAAGAA | 12488 |
rs33179100 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Cd2ap | Mm_Celera | 17:42840434 | CCTGGAATTCCTCAG[G/T]ATCTCTACTCCTGTG | 12488 |
rs33182667 | snp | A/G | 0.290657 | 0.246672 | intron-variant | Cd2ap | Mm_Celera | 17:42833978 | ATACAGATAAGCAAT[A/G]GGGTAAAACAGAATC | 12488 |
rs33187911 | snp | C/T | 0.375 | 0.216506 | downstream-variant-500B, intron-variant | Cd2ap | Mm_Celera | 17:42792745 | GTGAGGTGACCATGT[C/T]GCAAGAGGTGTGTCA | 12488 |
rs33191354 | snp | C/T | 0.32 | 0.24 | intron-variant | Cd2ap | Mm_Celera | 17:42835226 | TGTATGAGCATTTGC[C/T]TGAGTGTTTGTCTAC | 12488 |
rs33192437 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Cd2ap | Mm_Celera | 17:42874753 | GGGGAAGGTGAAAGG[C/T]GATACTAATCATAGT | 12488 |
rs33203454 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Cd2ap | Mm_Celera | 17:42854475 | AACCTACCTCTCAAG[A/G]CACTGGGGTAAGAGG | 12488 |
rs33204038 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Cd2ap | Mm_Celera | 17:42866888 | TGTTTTCCTACTACC[G/T]CTCAGTGCATGAGTA | 12488 |
rs33215526 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Cd2ap | Mm_Celera | 17:42872022 | TTCAAGAGGCAACGA[A/G]CACAATCTTCTAGCC | 12488 |
rs33216347 | snp | A/G | 0.375 | 0.216506 | intron-variant | Cd2ap | Mm_Celera | 17:42802814 | TTGGTGGACCTAAGA[A/G]TTCTACTTCTTGATC | 12488 |
rs33219330 | snp | C/G | 0.498615 | 0.0262793 | intron-variant | Cd2ap | GRCm38.p3 | 17:42752585 | TACTCCTTAGCCTTG[C/G]TTGCTTGCCAAGTCT | 12488 |
rs33219736 | snp | A/G | 0.375 | 0.216506 | intron-variant | Cd2ap | GRCm38.p3 | 17:42825268 | TGGACTTTCACAAGC[A/G]TGGCGTGTGTACCCC | 12488 |
rs33224014 | snp | C/G/T | 0.375 | 0.216506 | intron-variant | Cd2ap | GRCm38.p3 | 17:42873841 | AAGAACTAAAGACTA[C/G/T]TGGGAGGAAGGGACA | 12488 |
rs33243336 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Cd2ap | Mm_Celera | 17:42816378 | TAACAGAGCTCTGTA[A/G]GTCAAAGGTAGTTAA | 12488 |
rs33246202 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Cd2ap | Mm_Celera | 17:42814676 | AATCAACTGATTAAG[A/T]GAACTGAAGATAAAG | 12488 |
rs33247189 | snp | A/G | 0.375 | 0.216506 | intron-variant | Cd2ap | Mm_Celera | 17:42870902 | ATTTAACTGAGTTGA[A/G]TCTTTACAGCAGATA | 12488 |
rs33247320 | snp | A/C | 0.375 | 0.216506 | intron-variant | Cd2ap | Mm_Celera | 17:42778918 | TTGGAATTTCCCAAG[A/C]TGTCCCATGCTGAGA | 12488 |
rs33251820 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Cd2ap | Mm_Celera | 17:42867804 | GGCTAAATCTGCTTT[G/T]ATATGTTAAACAGAC | 12488 |
rs33252842 | snp | A/G | 0.375 | 0.216506 | intron-variant | Cd2ap | Mm_Celera | 17:42783178 | CTCAGAGTTACTGTA[A/G]TTCCATTTATTATTA | 12488 |
rs33252853 | snp | A/G | 0.375 | 0.216506 | intron-variant | Cd2ap | Mm_Celera | 17:42840216 | GTGACAGAGCAGAAT[A/G]CTTTATTTCTGTTCT | 12488 |
rs33255985 | snp | A/G | 0.188366 | 0.242283 | intron-variant | Cd2ap | Mm_Celera | 17:42834374 | AAATGGAGCTGTAAA[A/G]ATAAATGACAGGTAA | 12488 |
rs33265941 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Cd2ap | Mm_Celera | 17:42860727 | ACTCAGATCACAGCT[A/C]TCAGAAGGAAAATCC | 12488 |
rs33266074 | snp | C/T | 0.207612 | 0.24638 | intron-variant | Cd2ap | Mm_Celera | 17:42753917 | GTCTGAGAATGTTTC[C/T]TAAACGTCCTTAATG | 12488 |
rs33273732 | snp | A/G | 0.444444 | 0.157135 | upstream-variant-2KB | Cd2ap | Mm_Celera | 17:42877925 | AAGACTATTTATTGA[A/G]CAATACGTTCATTAT | 12488 |
rs33274251 | snp | A/G | 0.32 | 0.24 | intron-variant | Cd2ap | Mm_Celera | 17:42834762 | AATCTCAAACCAGTG[A/G]AATGATTCATCAGGT | 12488 |
rs33283275 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Cd2ap | Mm_Celera | 17:42784285 | TTTAAAGCACTAGAG[C/T]TGGGCAGATATCTAC | 12488 |
rs33284754 | snp | A/G | 0.32 | 0.24 | intron-variant | Cd2ap | Mm_Celera | 17:42779741 | ATAAATAAATAAATA[A/G]ATAAGATTAGATTAG | 12488 |
rs33287573 | snp | C/T | 0.375 | 0.216506 | intron-variant | Cd2ap | Mm_Celera | 17:42797794 | CTATCTCCCCCCACC[C/T]CACCCCCCACACTCC | 12488 |
rs33292087 | snp | A/G | 0.5 | 0 | intron-variant, downstream-variant-500B | Gpr111, Cd2ap | Mm_Celera | 17:42748868 | CTATCCTTTCATACA[A/G]CCAGACTGCAGTGAT | 12488 |
rs33297045 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Cd2ap | Mm_Celera | 17:42807543 | ACACGTTTTCTGAGG[A/G]AGTCTGGTCAACATA | 12488 |
rs33308426 | snp | A/G | 0.5 | 0 | intron-variant, downstream-variant-500B | Gpr111, Cd2ap | Mm_Celera | 17:42748810 | GGCAACATGAGTCTC[A/G]GAAAGAAAAAAGAAA | 12488 |
rs33318231 | snp | C/T | 0.375 | 0.216506 | intron-variant | Cd2ap | Mm_Celera | 17:42840199 | TTGTACAATCACACA[C/T]AGTGACAGAGCAGAA | 12488 |
rs33334932 | snp | A/G | 0.32 | 0.24 | intron-variant | Cd2ap | Mm_Celera | 17:42859675 | TATTTTTTGTCCTAA[A/G]TATTTCTCCTTTAAC | 12488 |
rs33335267 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Cd2ap | Mm_Celera | 17:42867204 | AAAAAGAAAAAGAAA[A/G]AGAAAGAAAAAGAAA | 12488 |
rs33335542 | snp | A/C | 0.375 | 0.216506 | intron-variant | Cd2ap | Mm_Celera | 17:42821039 | CAAAACAAAAAGAAA[A/C]ACACACACACACAAA | 12488 |
rs33339468 | snp | A/G | 0.375 | 0.216506 | upstream-variant-2KB | Cd2ap | Mm_Celera | 17:42878370 | AAACCCAGGTCCCCT[A/G]CAAGGACAGCAGGTG | 12488 |
rs33342728 | snp | A/C | 0.32 | 0.24 | intron-variant | Cd2ap | Mm_Celera | 17:42863391 | GTTGTTTCTCTAACT[A/C]TAAGAGTGACAACAG | 12488 |
rs33347741 | snp | A/G | 0.32 | 0.24 | intron-variant | Cd2ap | GRCm38.p3 | 17:42835217 | CACTTTATGTGTATG[A/G]GCATTTGCTTGAGTG | 12488 |
rs33348987 | snp | C/T | 0.375 | 0.216506 | intron-variant | Cd2ap | Mm_Celera | 17:42824239 | TGTAATGAGATCTGA[C/T]GCCCTCTTCTGGAGT | 12488 |
rs33352156 | snp | A/G | 0.375 | 0.216506 | intron-variant | Cd2ap | Mm_Celera | 17:42802885 | TATAGTTTGAGCACA[A/G]AAGACCTCAAAGCCT | 12488 |
rs33353031 | snp | C/T | 0.197531 | 0.244432 | intron-variant | Cd2ap | Mm_Celera | 17:42815082 | AACTTAACCAAGATG[C/T]CTGTGCTTCCAGCTC | 12488 |
rs33354725 | snp | A/T | 0.375 | 0.216506 | intron-variant | Cd2ap | Mm_Celera | 17:42787316 | CTCATATCTGGATAT[A/T]TAGACAGTCTGAACA | 12488 |
rs33355558 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Cd2ap | Mm_Celera | 17:42871995 | CCTGCTTCAGAGGGA[C/T]TGGTAAAATGGTTCA | 12488 |
rs33363977 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Cd2ap | Mm_Celera | 17:42868671 | GGTAAAAACTTCAGG[A/T]CGTAGAACACACTGG | 12488 |
rs33372208 | snp | A/G | 0.32 | 0.24 | intron-variant | Cd2ap | Mm_Celera | 17:42863315 | TCTATAGCACAGAGT[A/G]TTCAAACAGTGAACC | 12488 |
rs33375522 | snp | C/T | 0.32 | 0.24 | intron-variant | Cd2ap | Mm_Celera | 17:42780376 | ACTGCTACTGCTTAA[C/T]TGTTAGCATTACTCC | 12488 |
rs33378603 | snp | C/T | 0.375 | 0.216506 | intron-variant | Cd2ap | Mm_Celera | 17:42820371 | ATAAAACAATAAATA[C/T]TCCATCTTACTGAAG | 12488 |
rs33378957 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Cd2ap | Mm_Celera | 17:42839964 | TACATTTCTGTCTGC[A/C]CCTAAAACTAAGCTG | 12488 |
rs33382732 | snp | A/G | 0.375 | 0.216506 | intron-variant | Cd2ap | Mm_Celera | 17:42870861 | CCCTACCTCACCTAG[A/G]AAGACTTCCCGCCTG | 12488 |
rs33388763 | snp | A/G | 0.375 | 0.216506 | intron-variant | Cd2ap | Mm_Celera | 17:42840837 | AACTGTGATAGTATG[A/G]ATGAGAAGTGTTCCC | 12488 |
rs33392732 | snp | C/T | 0.375 | 0.216506 | intron-variant | Cd2ap | Mm_Celera | 17:42834484 | TATTAATTAGTCATG[C/T]ATGGAAATAATCATA | 12488 |
rs33405999 | snp | A/G | 0.375 | 0.216506 | intron-variant | Cd2ap | Mm_Celera | 17:42866407 | CATCATGTGGTTGCT[A/G]GGATTTGAATTCAGG | 12488 |
rs33409253 | snp | C/T | 0.375 | 0.216506 | intron-variant | Cd2ap | GRCm38.p3 | 17:42784207 | AGTGGTTTCTATCCC[C/T]GCTTTAAATCATTCA | 12488 |
rs33419342 | snp | C/T | 0.33241 | 0.236027 | utr-variant-3-prime, intron-variant | Cd2ap | Mm_Celera | 17:42795521 | GGTGTTTACATATTC[C/T]ACATGTGCTGCGGTG | 12488 |
rs33420806 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Cd2ap | Mm_Celera | 17:42858219 | AAAGGCAGAGGCAGG[C/T]GGATTTCTGAGTTCG | 12488 |
rs33436105 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Cd2ap | Mm_Celera | 17:42871969 | ATGAGCCCCAGGGTT[C/G]AGAGAAAGACCCTGC | 12488 |
rs33442505 | snp | A/G | 0.375 | 0.216506 | intron-variant | Cd2ap | Mm_Celera | 17:42871774 | TCTGCCTGTACACAG[A/G]GGGCTGGAGCGAGAG | 12488 |
rs33443001 | snp | A/G | 0.359862 | 0.224567 | intron-variant, downstream-variant-500B | Gpr111, Cd2ap | Mm_Celera | 17:42748950 | TAGAAAAGCAACATC[A/G]CTAACTCATGTAACA | 12488 |
rs33444842 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Cd2ap | Mm_Celera | 17:42834153 | TCGCACCACTTCAGC[A/G]TCTCCACCAACCTGA | 12488 |
rs33445338 | snp | A/G | 0.32 | 0.24 | intron-variant | Cd2ap | Mm_Celera | 17:42863536 | GCAGTGATGGCACAC[A/G]CCTTTAATCCTAGCA | 12488 |
rs33446116 | snp | C/G | 0.375 | 0.216506 | intron-variant | Cd2ap | Mm_Celera | 17:42860365 | GACACCTACTGTGTA[C/G]TAGTTACTTTTACTA | 12488 |
rs33446199 | snp | A/C | 0.375 | 0.216506 | intron-variant | Cd2ap | Mm_Celera | 17:42858704 | GAGGCAGACAGATAT[A/C]TGAATTTAAGGCCAG | 12488 |
rs33451124 | snp | A/G | 0.375 | 0.216506 | intron-variant | Cd2ap | GRCm38.p3 | 17:42787411 | CTGTGGAAAAGAGAC[A/G]CTATGGCCCTTATCA | 12488 |
rs33476252 | snp | A/G | 0.18 | 0.24 | intron-variant | Cd2ap | Mm_Celera | 17:42835003 | TCCTGGAAATCAGCC[A/G]CCTCCAAGCAGCTCA | 12488 |
rs33481662 | snp | C/T | 0.375 | 0.216506 | intron-variant | Cd2ap | Mm_Celera | 17:42866565 | TCACCAAAAAACATC[C/T]GGCAATAGTGAGAGG | 12488 |
rs33482505 | snp | A/G | 0.32 | 0.24 | intron-variant | Cd2ap | Mm_Celera | 17:42859781 | TAGATCCATGTGAAA[A/G]TATTGGATCCATTAT | 12488 |
rs33482511 | snp | G/T | 0.375 | 0.216506 | intron-variant | Cd2ap | Mm_Celera | 17:42871765 | GATAAGACATCTGCC[G/T]GTACACAGAGGGCTG | 12488 |
rs33485940 | snp | A/G | 0.32 | 0.24 | intron-variant | Cd2ap | Mm_Celera | 17:42845251 | CAGAAGACAGCACTC[A/G]TCTTTCTGAGTTTAT | 12488 |
rs33487841 | snp | C/T | 0.265928 | 0.249492 | intron-variant | Cd2ap | Mm_Celera | 17:42840407 | ACACAGAATGTATTC[C/T]ACCACACAAAGCCTG | 12488 |
rs33489166 | snp | A/G | 0.375 | 0.216506 | intron-variant | Cd2ap | Mm_Celera | 17:42866034 | ACACTTTCTGCTGGA[A/G]ACCTACATAAGGACA | 12488 |
rs33489173 | snp | A/T | 0.5 | 0 | intron-variant | Cd2ap | Mm_Celera | 17:42786007 | AAATAAATCTTTTTT[A/T]AAAAAAAGAAAAGAA | 12488 |
rs33490978 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Cd2ap | Mm_Celera | 17:42862685 | CCCACCCCCCACCCC[C/T]GCTCCCCCTGCTCAC | 12488 |
rs33505785 | snp | A/G | 0.375 | 0.216506 | intron-variant | Cd2ap | GRCm38.p3 | 17:42792210 | TGGAAATGTAATTGA[A/G]GAAAGTACCTAATTT | 12488 |
rs33509273 | snp | A/T | 0.5 | 0 | intron-variant | Cd2ap | Mm_Celera | 17:42800854 | GTGGTTTGAACAGGA[A/T]CTGAACTCATAGACT | 12488 |
rs33509483 | snp | C/T | 0.492188 | 0.0620098 | intron-variant | Cd2ap | Mm_Celera | 17:42817915 | AATAGCAGGAAGGGG[C/T]CTTTGCTTAATTTAC | 12488 |
rs33517403 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Cd2ap | Mm_Celera | 17:42839979 | ACCTAAAACTAAGCT[A/G]CACAGGTCTAGCTGC | 12488 |
rs33517946 | snp | C/T | 0.375 | 0.216506 | intron-variant | Cd2ap | Mm_Celera | 17:42817312 | CAGCAGTTAAGAGCA[C/T]TGGCTGCTCCTGCAG | 12488 |
rs33522002 | snp | A/G | 0.375 | 0.216506 | intron-variant | Cd2ap | Mm_Celera | 17:42858203 | TTAATCCCAGCACTC[A/G]AAAGGCAGAGGCAGG | 12488 |
rs33522003 | snp | A/C | 0.375 | 0.216506 | intron-variant | Cd2ap | Mm_Celera | 17:42870855 | CTGCCCCCCTACCTC[A/C]CCTAGAAAGACTTCC | 12488 |
rs33523496 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Cd2ap | Mm_Celera | 17:42841359 | TGGAGTTTATAATGG[A/G]CAGAGATCACAAATT | 12488 |
rs33524196 | snp | C/T | 0.32 | 0.24 | intron-variant | Cd2ap | Mm_Celera | 17:42753549 | CTCTCTCTCCTCTCT[C/T]TCTCTCTCTCCCTGT | 12488 |
rs33530756 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Cd2ap | Mm_Celera | 17:42873209 | GCAATATTCTAAGCA[C/T]TGTTAGGTCATTCAT | 12488 |
rs33535223 | snp | G/T | 0.375 | 0.216506 | intron-variant | Cd2ap | Mm_Celera | 17:42800832 | AAGAGAAAGAAAACA[G/T]TGTGTGGTGGTTTGA | 12488 |
rs33540280 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Cd2ap | Mm_Celera | 17:42753895 | TTTTTTCCAGGCAGC[A/T]AACCTGGTCTGAGAA | 12488 |
rs33541804 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Cd2ap | Mm_Celera | 17:42854552 | AAAATAAAGACAAGA[C/T]GTGACACCCAAAACT | 12488 |
rs33544210 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Cd2ap | Mm_Celera | 17:42844541 | AGGTTAAGAGCACTG[C/T]CTCCTCTTCCAGAGG | 12488 |
rs33544731 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Cd2ap | GRCm38.p3 | 17:42854350 | TCATTTGATCTTTAA[A/G]GGAACATAGCTCCAC | 12488 |
rs33549163 | snp | A/G | 0.32 | 0.24 | intron-variant | Cd2ap | Mm_Celera | 17:42855294 | CACAAAATGTTAATT[A/G]GCTTGGCATTTTTCT | 12488 |
rs33565705 | snp | A/G | 0.375 | 0.216506 | intron-variant | Cd2ap | GRCm38.p3 | 17:42784215 | CTATCCCTGCTTTAA[A/G]TCATTCAGTCCCCAG | 12488 |
rs33568997 | snp | C/T | 0.5 | 0 | intron-variant | Cd2ap | Mm_Celera | 17:42799380 | TCTGCCAGAACCTGA[C/T]ATATTCAGAGGTGGA | 12488 |
rs33570535 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Cd2ap | Mm_Celera | 17:42860641 | ACAAAACAAAAGCCC[A/C]CGGGACAGCCCATAC | 12488 |
rs33576991 | snp | A/G | 0.375 | 0.216506 | intron-variant | Cd2ap | Mm_Celera | 17:42858208 | CCCAGCACTCAAAAG[A/G]CAGAGGCAGGTGGAT | 12488 |
rs33593493 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Cd2ap | Mm_Celera | 17:42840676 | ACTGAATTTAGGACC[A/G]CCTGTCACTGTTTCT | 12488 |
rs33593676 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Cd2ap | Mm_Celera | 17:42871993 | ACCCTGCTTCAGAGG[A/G]ACTGGTAAAATGGTT | 12488 |
rs33594712 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Cd2ap | Mm_Celera | 17:42834132 | AAGTAAGAGATACAG[C/T]CAGAGTCGCACCACT | 12488 |
rs33597116 | snp | A/G | 0.32 | 0.24 | intron-variant | Cd2ap | GRCm38.p3 | 17:42777248 | CGATGAAGCAGGCAG[A/G]AACAATCAGAACTAA | 12488 |
rs33598991 | snp | C/T | 0.32 | 0.24 | intron-variant | Cd2ap | Mm_Celera | 17:42780357 | TTGATAAGCATTAGC[C/T]ATCACTGCTACTGCT | 12488 |
rs33599658 | snp | C/T | 0.375 | 0.216506 | intron-variant | Cd2ap | Mm_Celera | 17:42840697 | CACTGTTTCTCAAAC[C/T]GGCTGGCCTCATTTA | 12488 |
rs33608788 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Cd2ap | Mm_Celera | 17:42866052 | CTACATAAGGACATT[G/T]GAAGAAGGAATATAC | 12488 |
rs33610019 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Cd2ap | Mm_Celera | 17:42860699 | AGTATGCAAAGATGT[A/G]CACAGTATATATACT | 12488 |
rs33610870 | snp | C/T | 0.375 | 0.216506 | intron-variant | Cd2ap | Mm_Celera | 17:42818334 | AAACTCTAAACAAGT[C/T]ATAGTTTTAAATATA | 12488 |
rs33611790 | snp | A/C | 0.5 | 0 | intron-variant | Cd2ap | Mm_Celera | 17:42801101 | AGCCAAACCTCTAAA[A/C]TTGTAAGCCAGCCCC | 12488 |
rs33621208 | snp | A/G | 0.375 | 0.216506 | intron-variant | Cd2ap | Mm_Celera | 17:42841254 | TGCCCAAAGAAAGGG[A/G]TGTTCTGTTTTAGTA | 12488 |
rs33624693 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Cd2ap | GRCm38.p3 | 17:42810803 | CCAATTATGGGGGGG[A/G]AAATCTGATTTGTAA | 12488 |
rs33631977 | snp | A/G | 0.375 | 0.216506 | intron-variant | Cd2ap | Mm_Celera | 17:42858205 | AATCCCAGCACTCAA[A/G]AGGCAGAGGCAGGTG | 12488 |
rs33643554 | snp | A/T | 0.375 | 0.216506 | intron-variant | Cd2ap | Mm_Celera | 17:42844914 | TAAAAAAAAAATAAA[A/T]AAAAAAACAAATAGA | 12488 |
rs33648854 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Cd2ap | Mm_Celera | 17:42839097 | CTACGAAGACATTTT[A/G]ACAATAAAATGATTG | 12488 |
rs33650785 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Cd2ap | Mm_Celera | 17:42827231 | CCTGTGCACCGAGTG[C/T]CCATGGAGGTCAAAG | 12488 |
rs33651617 | snp | C/T | 0.375 | 0.216506 | intron-variant | Cd2ap | Mm_Celera | 17:42780066 | CCCTCTTTTGGCTAC[C/T]ATGAGCTATGTATTC | 12488 |
rs33664446 | snp | A/T | 0.375 | 0.216506 | intron-variant | Cd2ap | Mm_Celera | 17:42873846 | CTAAAGACTAGTGGG[A/T]GGAAGGGACAGTAAG | 12488 |
rs33666329 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Cd2ap | Mm_Celera | 17:42813211 | CATTTGAGTGGCAAC[A/G]TGACTACCAGTGGAT | 12488 |
rs33670129 | snp | A/G | 0.375 | 0.216506 | intron-variant | Cd2ap | Mm_Celera | 17:42863605 | CCAGCCTGGTCTACT[A/G]TGTGAGTTCCAGGAC | 12488 |
rs33671548 | snp | A/G/T | 0.375 | 0.216506 | intron-variant | Cd2ap | GRCm38.p3 | 17:42753356 | ATCTGAGACAGGAGG[A/G/T]TTAGGAGACCGGTTT | 12488 |
rs33673179 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Cd2ap | Mm_Celera | 17:42866066 | TGGAAGAAGGAATAT[A/T]CGCTCTTCTTTGCCT | 12488 |
rs33678453 | snp | A/G | 0.444444 | 0.157135 | upstream-variant-2KB, intron-variant | Gpr111, Cd2ap | Mm_Celera | 17:42750056 | AGTAGGCAATGGATG[A/G]GGCCAAAATTCCCAC | 12488 |
rs33679198 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Cd2ap | Mm_Celera | 17:42753896 | TTTTTCCAGGCAGCA[A/C]ACCTGGTCTGAGAAT | 12488 |
rs33680719 | snp | A/G | 0.444444 | 0.157135 | upstream-variant-2KB, intron-variant | Gpr111, Cd2ap | Mm_Celera | 17:42750163 | GGACAAGCTTTCCCA[A/G]GTGCTGTAGCTCATG | 12488 |
rs33683237 | snp | A/G | 0.32 | 0.24 | intron-variant | Cd2ap | Mm_Celera | 17:42863527 | TCAGGCCAGGCAGTG[A/G]TGGCACACGCCTTTA | 12488 |
rs33689838 | snp | A/T | 0.375 | 0.216506 | intron-variant | Cd2ap | Mm_Celera | 17:42866366 | AGAGGGCGTCAGATC[A/T]CATTACATTATGGAT | 12488 |
rs33690672 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Cd2ap | GRCm38.p3 | 17:42805677 | TGTGTGTGTGTGTGT[A/G]TATATATATATATAT | 12488 |
rs33692531 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Cd2ap | Mm_Celera | 17:42864437 | CTACAGTTAGTTCTA[A/G]GCCAGCCTAAGCAAC | 12488 |
rs33692822 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Cd2ap | Mm_Celera | 17:42866617 | AATATTAATTCAAAA[A/T]TCAACCATAAAATGA | 12488 |
rs33697483 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Cd2ap | GRCm38.p3 | 17:42788919 | TTAGATGGAGCTTGA[A/G]GACTCTTACGGAAGA | 12488 |
rs33701153 | snp | C/T | 0.375 | 0.216506 | intron-variant | Cd2ap | Mm_Celera | 17:42869925 | GTGGGCATAAGGAAT[C/T]CAAAGCTAGGTCAGT | 12488 |
rs33718972 | snp | A/C | 0.197531 | 0.244432 | intron-variant | Cd2ap | Mm_Celera | 17:42840124 | GCAGCAGATCAGAGA[A/C]ATTTAACTTTCTGCT | 12488 |
rs45670359 | snp | C/G/T | 0.124444 | 0.216185 | intron-variant | Cd2ap | Mm_Celera | 17:42754029 | ATCCAGCTTCTGGGA[C/G/T]ACTCATTAACTAGAA | 12488 |
rs45677171 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Cd2ap | Mm_Celera | 17:42751977 | CTGTTGCTAGTCATC[A/G]GGTTCTCTGCATAGG | 12488 |
rs45681038 | snp | C/T | 0.124444 | 0.216185 | missense, nc-transcript-variant | Cd2ap | GRCm38.p3 | 17:42826311 | CAACGTCTGGTTTTG[C/T]TACCTCCACATTCTG | 12488 |
rs45688017 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Cd2ap | Mm_Celera | 17:42834051 | TTTTCCCTTTTATTC[C/T]CATGATACTTTGGTT | 12488 |
rs45693617 | snp | C/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42813787 | TGAGTGTATAGAAAA[C/T]TTGAGGGCTTGGAAA | 12488 |
rs45701589 | snp | C/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42813331 | TCAAAGTCACACATG[C/T]AGACATTTTGTTCGA | 12488 |
rs45704993 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Cd2ap | Mm_Celera | 17:42816947 | ATTATGAATAACTGT[A/C]TGCCACATTCGTTAA | 12488 |
rs45713321 | snp | C/T | 0.231111 | 0.249285 | utr-variant-3-prime, intron-variant | Cd2ap | Mm_Celera | 17:42793950 | GCTACTCTGATTGTG[C/T]GGACTAAAAATACCC | 12488 |
rs45724111 | snp | C/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42848850 | AAGACAGCTACCTTA[C/T]TTAATCTGCCCTTGC | 12488 |
rs45726794 | snp | A/C | | | intron-variant | Cd2ap | Mm_Celera | 17:42832717 | TCAAATAAAAGACAA[A/C]TGAAATTAAAGGGTT | 12488 |
rs45736999 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Cd2ap | Mm_Celera | 17:42796810 | AGAAGCTGAAGATGC[C/T]GAGATCTGCCATCAG | 12488 |
rs45740386 | snp | C/T | 0.132653 | 0.220748 | intron-variant, upstream-variant-2KB | Cd2ap | Mm_Celera | 17:42829733 | CTGATGGCTGGCTCC[C/T]ATGGGAATCTGTGCT | 12488 |
rs45757151 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Cd2ap | Mm_Celera | 17:42826790 | TCTCAGTGGCAGCAA[A/G]GTCTGAATTAGCCTG | 12488 |
rs45762978 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Cd2ap | Mm_Celera | 17:42838625 | AATTTTCACTAATTT[C/G]TATATTCCGACAAAG | 12488 |
rs45784202 | snp | A/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42836413 | TACAAATAGCTAGAA[A/T]ACAGTATATTTGGGA | 12488 |
rs45798418 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Cd2ap | Mm_Celera | 17:42755094 | ACCCATATGGAACTT[C/T]CCCAAGCTTGCAGTA | 12488 |
rs45817002 | snp | A/G | | | upstream-variant-2KB | Cd2ap | Mm_Celera | 17:42877939 | AGCAATACGTTCATT[A/G]TCTCCTCCCAAGCAA | 12488 |
rs45831681 | snp | C/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42870281 | GATGCTAGACTGTAA[C/T]CAAGGAATACTCTCA | 12488 |
rs45835033 | snp | C/G | | | intron-variant | Cd2ap | Mm_Celera | 17:42833654 | GAACTCATGAGAACT[C/G]TTTCTTTTTTTTATG | 12488 |
rs45848988 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Cd2ap | Mm_Celera | 17:42837563 | ATCTAATGCAAATGG[A/G]AAGGACTCTAAATAG | 12488 |
rs45946458 | snp | C/T | | | upstream-variant-2KB | Cd2ap | GRCm38.p3 | 17:42877150 | CATAGGCATACATTA[C/T]TGTATTCCTTGAGTC | 12488 |
rs45950182 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Cd2ap | Mm_Celera | 17:42752793 | TATTAACTTGCTGAC[C/T]CCTATGGAAATTCCC | 12488 |
rs45962235 | snp | A/C | | | intron-variant | Cd2ap | Mm_Celera | 17:42781927 | AACTGGATTGATAGG[A/C]CAGCCATACATACAG | 12488 |
rs45964060 | snp | C/G | | | upstream-variant-2KB | Cd2ap | GRCm38.p3 | 17:42876747 | CGCCACCCAGGCTCC[C/G]GCAGCTGGTGCCAGG | 12488 |
rs45998260 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Cd2ap | Mm_Celera | 17:42756392 | GCTTCCATCACTCAC[A/G]AAGTCAGTAACTTCT | 12488 |
rs46012384 | snp | A/T | 0.493827 | 0.0552116 | intron-variant | Cd2ap | Mm_Celera | 17:42827563 | CATCAAAGCAGCAAC[A/T]GCAGCCCTAAAGCTC | 12488 |
rs46028920 | snp | A/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42850382 | AATAAGCTGAAAATT[A/T]TAAATGCATAAAAAC | 12488 |
rs46056347 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Cd2ap | Mm_Celera | 17:42751647 | GAAGAAACAGAAGGC[A/G]GAGATTCAAGCTGGG | 12488 |
rs46082239 | snp | A/C | | | intron-variant | Cd2ap | Mm_Celera | 17:42832316 | CCAGAAAAGGGCATC[A/C]GATCTCATTACGGAT | 12488 |
rs46087364 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Cd2ap | Mm_Celera | 17:42812755 | GCGAAGTCAGAGTGG[C/T]TTCTACCATACTATT | 12488 |
rs46106857 | snp | C/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42849466 | GGGATGGACCACTCC[C/T]TCATAATCAGCAGCC | 12488 |
rs46113079 | snp | A/C | | | intron-variant | Cd2ap | GRCm38.p3 | 17:42807145 | TCAATTAAAATTATA[A/C]TTTTAGAAAAGAAAC | 12488 |
rs46127329 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Cd2ap | Mm_Celera | 17:42751464 | AACCTGGAATAAATG[C/T]CTTCCCGGTATCTAC | 12488 |
rs46174894 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Cd2ap | Mm_Celera | 17:42755487 | AACAAGGTGAGATAT[A/T]CTTTGCTTTACACAT | 12488 |
rs46179603 | snp | A/T | | | intron-variant, upstream-variant-2KB | Cd2ap | Mm_Celera | 17:42830991 | CATAAAATACTTTTT[A/T]AAAAATCCCAAATAT | 12488 |
rs46182096 | snp | C/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42869657 | CACTAGAACACATCC[C/T]TCCTTAAATGGCTTG | 12488 |
rs46196327 | snp | C/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42775564 | TCACCTGAGGAATAC[C/T]GAAAGGCTAAGAAAC | 12488 |
rs46210173 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Cd2ap | Mm_Celera | 17:42818294 | CCTGTAAAGTGTCTT[C/T]GGAACAGGCTAAAGA | 12488 |
rs46219678 | snp | A/C | | | intron-variant | Cd2ap | Mm_Celera | 17:42781684 | AGAAACAGAAGATAG[A/C]CTATCCAGAAACTCA | 12488 |
rs46219797 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Cd2ap | GRCm38.p3 | 17:42838633 | CTAATTTGTATATTC[C/T]GACAAAGCCCTCCTC | 12488 |
rs46222767 | snp | A/T | 0.32 | 0.24 | intron-variant | Cd2ap | Mm_Celera | 17:42813174 | TGAAATGTCCAAAAT[A/T]GAAAATTCATCAAAA | 12488 |
rs46236881 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Cd2ap | Mm_Celera | 17:42833934 | ATTATTAAGCTAGGC[C/T]ATTAACAAACTCAGC | 12488 |
rs46249844 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Cd2ap | Mm_Celera | 17:42753939 | TCCTTAATGCTTAAA[G/T]AAACTTGGACTGGGA | 12488 |
rs46252816 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Cd2ap | Mm_Celera | 17:42752053 | TCAATAGGTAATGCT[A/G]CTTCTCTGGTTGTCA | 12488 |
rs46260782 | snp | A/G | | | intron-variant | Cd2ap | Mm_Celera | 17:42798177 | ACTACCCCAAGAGAG[A/G]AGCTGACCAGGACGC | 12488 |
rs46294856 | snp | C/T | | | intron-variant | Cd2ap | GRCm38.p3 | 17:42774272 | CAATCCCACTAAAAT[C/T]AGGGACTAGACAAGG | 12488 |
rs46310478 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Cd2ap | Mm_Celera | 17:42838349 | TATTATAGTGGTGTG[C/T]GTACATAATGTGAGT | 12488 |
rs46331505 | snp | A/G | | | intron-variant | Cd2ap | Mm_Celera | 17:42869122 | CCATCTCTCCAGCAC[A/G]TTTATACAGTCTTGC | 12488 |
rs46362868 | snp | A/G | | | intron-variant | Cd2ap | Mm_Celera | 17:42872163 | GCAGCCTGGTCTACA[A/G]AGTGAGTTCCAGGAC | 12488 |
rs46461285 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Cd2ap | Mm_Celera | 17:42825088 | ACATGGCCTTAGAAT[C/T]TATCCTAATTTAAGC | 12488 |
rs46462311 | snp | A/G | | | intron-variant | Cd2ap | Mm_Celera | 17:42807433 | GAGTGGACAAACCAT[A/G]ACTCCAATCTGCTAA | 12488 |
rs46506558 | snp | A/C/G | 0.124444 | 0.216185 | intron-variant | Cd2ap | GRCm38.p3 | 17:42754009 | ACCAGCAGCCTCAGC[A/C/G]TCAGATCCAGCTTCT | 12488 |
rs46534089 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Cd2ap | Mm_Celera | 17:42756977 | TGCTCTAGTCTAAAC[A/G]GGAGTTACAAGCAAT | 12488 |
rs46546377 | snp | C/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42853726 | TCTGATCACAGGCAG[C/T]ATACAGGTACATTTT | 12488 |
rs46551782 | snp | A/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42849931 | AGTAAAACCCATCTT[A/T]AAAAAAAAAAAAAAA | 12488 |
rs46575546 | snp | A/T | 0.152778 | 0.230321 | intron-variant | Cd2ap | Mm_Celera | 17:42821859 | CTGAAGTACCCAAGC[A/T]ACCTCTAAGATCCCC | 12488 |
rs46578847 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Cd2ap | Mm_Celera | 17:42756462 | ATGATCATCAAGCTC[A/G]CTTTACGACTGTAGT | 12488 |
rs46582171 | snp | C/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42798210 | GAAGGCAAAAGCCTG[C/T]TTGCCCCTTAAGGTA | 12488 |
rs46597978 | snp | C/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42848852 | GACAGCTACCTTATT[C/T]AATCTGCCCTTGCCA | 12488 |
rs46604403 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Cd2ap | GRCm38.p3 | 17:42820713 | TAATATACACAGAAA[A/G]AACAAAAATATGGTA | 12488 |
rs46608795 | snp | C/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42845899 | ACAGTAGCTTTAAGT[C/T]AAGAGTTCATAAACT | 12488 |
rs46617105 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Cd2ap | Mm_Celera | 17:42816770 | TTAAAAAATGATCCA[C/T]GGGAGCCAGAACTCA | 12488 |
rs46620486 | snp | A/G | | | intron-variant | Cd2ap | Mm_Celera | 17:42865253 | ATAGTGGTGCACATG[A/G]TAATCCCAGTATTTG | 12488 |
rs46637930 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Cd2ap | Mm_Celera | 17:42809767 | TCAGTGTAAGTTCCT[A/G]CAGCTCAGATAACAA | 12488 |
rs46664595 | snp | A/C | | | intron-variant | Cd2ap | GRCm38.p3 | 17:42774326 | TCAACATAGTACTTG[A/C]AGTCCTAGCCAGAGC | 12488 |
rs46668865 | snp | A/G | | | intron-variant | Cd2ap | Mm_Celera | 17:42798148 | TCCAGTCCAGGCCAG[A/G]CCGAATGGGCCTGAC | 12488 |
rs46669415 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Cd2ap | Mm_Celera | 17:42840383 | CCCAGGGTAGGAAGG[A/G]GTTACACCACACAGA | 12488 |
rs46681121 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Cd2ap | Mm_Celera | 17:42839327 | CAAAAGCCTTAGAAA[A/G]CCTACAGCTGCAGAG | 12488 |
rs46694603 | snp | A/G | 0.32 | 0.24 | intron-variant | Cd2ap | Mm_Celera | 17:42810237 | TAAATGTAAGCATAT[A/G]TCATTCTGTTTATAA | 12488 |
rs46721611 | snp | C/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42798092 | CACTTCCAAACAAGA[C/T]GGTGCCTGCACCCAC | 12488 |
rs46726836 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Cd2ap | Mm_Celera | 17:42751855 | TATAACACCCTCTAC[C/G]AGAACCTGCCACTAA | 12488 |
rs46752245 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Cd2ap | Mm_Celera | 17:42833431 | GGGTCATTACAAAAG[C/T]ACAATAAACCAATTA | 12488 |
rs46786201 | snp | C/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42872129 | GGAGGCAGAGGCAGG[C/T]GGATTTCTGAGTTTG | 12488 |
rs46834022 | snp | A/G | | | intron-variant | Cd2ap | Mm_Celera | 17:42841601 | CACATATAATAATAA[A/G]ATAAAAAATTAAAAG | 12488 |
rs46838366 | snp | A/C | | | intron-variant | Cd2ap | Mm_Celera | 17:42836526 | ACCATAGAACTTACA[A/C]TACAAGGGCGGAAGC | 12488 |
rs46839954 | snp | A/G | | | intron-variant | Cd2ap | Mm_Celera | 17:42825974 | ACTTACAAGTTGATT[A/G]ATGTAGCAGGTACTT | 12488 |
rs46884893 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Cd2ap | Mm_Celera | 17:42803734 | GTCAGGAGAGTGTCC[C/T]AATTGGTGATGGTAT | 12488 |
rs46896103 | snp | A/C | 0.165289 | 0.235211 | intron-variant | Cd2ap | Mm_Celera | 17:42836343 | TAGATAAAAAGCATG[A/C]GGGTGAAAAAAGTCA | 12488 |
rs46899467 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Cd2ap | Mm_Celera | 17:42754213 | CTATCCCCACAAAAG[A/G]CGTGTGGAATGAGTT | 12488 |
rs46913960 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Cd2ap | Mm_Celera | 17:42826710 | GTTGGTTATGTCAGG[A/G]ATCCCTCAGGAAGAC | 12488 |
rs46916099 | snp | A/G | | | intron-variant | Cd2ap | Mm_Celera | 17:42833439 | ACAAAAGTACAATAA[A/G]CCAATTAAAGAAGTC | 12488 |
rs46918508 | snp | A/G | | | intron-variant, upstream-variant-2KB | Cd2ap | Mm_Celera | 17:42831027 | GGCATGGTGGCGCAC[A/G]CCTTTAATCCCAGCA | 12488 |
rs46975365 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Cd2ap | Mm_Celera | 17:42821839 | TTAACTCAATATTCC[A/C]ATTACTGAAGTACCC | 12488 |
rs46989344 | snp | A/C | | | intron-variant | Cd2ap | Mm_Celera | 17:42842049 | AAAAGATATTATAAT[A/C]TCAACAATCTCAGGT | 12488 |
rs46996400 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Cd2ap | Mm_Celera | 17:42755183 | AGTGATGGTGAGAGT[C/T]CTTACTCAAAAGCTC | 12488 |
rs47003270 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Cd2ap | Mm_Celera | 17:42838966 | TTATAAACACCTCTC[A/C]CATGACATATTATGT | 12488 |
rs47010913 | snp | A/G | 0.375 | 0.216506 | intron-variant | Cd2ap | GRCm38.p3 | 17:42835127 | ATAATTTCCTAAGTG[A/G]TATAAAATTTTATTT | 12488 |
rs47056441 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Cd2ap | Mm_Celera | 17:42752676 | ACATAGATAACCGAA[C/T]GCATCATGCAGAGAA | 12488 |
rs47058196 | snp | C/T | 0.391111 | 0.206368 | upstream-variant-2KB, intron-variant | Gpr111, Cd2ap | Mm_Celera | 17:42750554 | CTTCCCATGGTGCCA[C/T]AGGTCTGTTATAGAA | 12488 |
rs47060001 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Cd2ap | Mm_Celera | 17:42752940 | GTATATGTTTGCATG[C/G]GAACTGGCTCCTTGG | 12488 |
rs47087689 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Cd2ap | GRCm38.p3 | 17:42823328 | AAAACCTAACTACTA[A/C]GAACATGAAACTGAA | 12488 |
rs47101570 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Cd2ap | Mm_Celera | 17:42838167 | CTTCAATGAGAAAAG[A/C]AATTAAATGCAACAA | 12488 |
rs47134153 | snp | A/G | | | intron-variant | Cd2ap | Mm_Celera | 17:42836344 | AGATAAAAAGCATGC[A/G]GGTGAAAAAAGTCAC | 12488 |
rs47137458 | snp | C/G | | | intron-variant | Cd2ap | Mm_Celera | 17:42849825 | AAAGAGTCAATCCAG[C/G]CAGGCATGGTGGCAT | 12488 |
rs47138719 | snp | A/T | | | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | Cd2ap | GRCm38.p3 | 17:42876646 | AAGCCACGGGCCCAG[A/T]GTGAAGAGAGTCGGG | 12488 |
rs47181465 | snp | G/T | 0.277778 | 0.248452 | intron-variant | Cd2ap | Mm_Celera | 17:42821122 | TTCAAAATAAATACA[G/T]GAATAAAAAAGTAGA | 12488 |
rs47185215 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Cd2ap | Mm_Celera | 17:42825140 | AGGTGTACTAAGACT[A/G]GGAACATGGCTCGGC | 12488 |
rs47199563 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Cd2ap | Mm_Celera | 17:42835935 | AAGATTCAAATCTTG[C/T]CTCTGAGAAATCCCT | 12488 |
rs47223263 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Cd2ap | Mm_Celera | 17:42752698 | TGCAGAGAACAGATA[A/G]CCTAGCCATCCTGTT | 12488 |
rs47239836 | snp | C/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42849826 | AAGAGTCAATCCAGC[C/T]AGGCATGGTGGCATG | 12488 |
rs47251611 | snp | A/G | | | intron-variant, upstream-variant-2KB | Cd2ap | GRCm38.p3 | 17:42830315 | TATATTTATTTGTAT[A/G]ACTAAGAAATTCAGG | 12488 |
rs47262908 | snp | A/G | | | intron-variant | Cd2ap | Mm_Celera | 17:42837068 | TCAGACTCTGGCTCA[A/G]AAACACCAAGGGCCC | 12488 |
rs47267662 | snp | A/G | | | intron-variant | Cd2ap | GRCm38.p3 | 17:42791865 | TTGTGAGACTAGGCC[A/G]GGGCCTAGCAAACAC | 12488 |
rs47268497 | snp | A/T | 0.391111 | 0.206368 | utr-variant-5-prime, utr-variant-3-prime | Gpr111, Cd2ap | Mm_Celera | 17:42749108 | ACATCACTGTGAAGA[A/T]GGACTGAGCTCCATT | 12488 |
rs47298808 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Cd2ap | Mm_Celera | 17:42752624 | GATGGCAGCAATGGG[A/G]CAACAGCCAGTCAAG | 12488 |
rs47318432 | snp | A/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42850805 | TTACCCAAAATGCAC[A/T]CCACAGAGAAGATGT | 12488 |
rs47321421 | snp | A/G | | | upstream-variant-2KB | Cd2ap | GRCm38.p3 | 17:42876897 | GGTTCTGCAAAATGA[A/G]CCCCGGTTACCCCAC | 12488 |
rs47394920 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Cd2ap | Mm_Celera | 17:42755251 | CCTCAGTGGTCTTTG[A/G]GGTCCTTGTGACTTG | 12488 |
rs47424286 | snp | A/G | | | intron-variant | Cd2ap | Mm_Celera | 17:42798113 | CTGCACCCACCTGCA[A/G]CTGGCTAAGATTCCC | 12488 |
rs47435753 | snp | C/T | 0.375 | 0.216506 | intron-variant | Cd2ap | Mm_Celera | 17:42854100 | CACTTCCATTCCATT[C/T]TGCTCAGAAAGTCTG | 12488 |
rs47441307 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Cd2ap | GRCm38.p3 | 17:42837566 | TAATGCAAATGGGAA[A/G]GACTCTAAATAGCTG | 12488 |
rs47475557 | snp | A/G | 0.244898 | 0.249948 | intron-variant, upstream-variant-2KB | Cd2ap | GRCm38.p3 | 17:42830868 | GCTCAAATGTACACT[A/G]ACAGTCACTGAACTA | 12488 |
rs47482747 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Cd2ap | Mm_Celera | 17:42819794 | ATTTCTGAGTACGTG[A/T]GTGCATGATAGGGGT | 12488 |
rs47521034 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Cd2ap | Mm_Celera | 17:42756703 | TTAGCAGAGTGTTTT[C/T]TATGCACTGTGTCAT | 12488 |
rs47535855 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Cd2ap | Mm_Celera | 17:42791436 | TGCTCTGTATGTTCT[A/G]TCTTCCAGCAAATAT | 12488 |
rs47538488 | snp | C/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42872143 | GCGGATTTCTGAGTT[C/T]GAGGGCAGCCTGGTC | 12488 |
rs47545915 | snp | C/T | | | synonymous-codon, nc-transcript-variant | Cd2ap | GRCm38.p3 | 17:42852512 | AGCATCATAGTCATA[C/T]TCCACAATATAGTCA | 12488 |
rs47571809 | snp | C/T | 0.375 | 0.216506 | intron-variant | Cd2ap | Mm_Celera | 17:42833269 | CTAGTCCCCAAAATA[C/T]TAGAAAAACAATGCA | 12488 |
rs47573790 | snp | A/G | | | intron-variant | Cd2ap | Mm_Celera | 17:42781752 | AAGGAACTGTAGAAG[A/G]GATGCATTTCTCTCT | 12488 |
rs47610749 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Cd2ap | Mm_Celera | 17:42831887 | ACAAGCACTCAATAT[A/G]CTAAAAAGAAACAAA | 12488 |
rs47625485 | snp | C/T | | | intron-variant, upstream-variant-2KB | Cd2ap | Mm_Celera | 17:42830273 | ATTGAATTCTGTTGA[C/T]AAATTGAATAAAACA | 12488 |
rs47646068 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Cd2ap | Mm_Celera | 17:42798401 | GAAGCACAAGGCCCC[A/G]TGTGTGATTCGCAAA | 12488 |
rs47649253 | snp | A/C | | | intron-variant | Cd2ap | Mm_Celera | 17:42835691 | CTCATTTAAATAAAT[A/C]GTTTTCAATGTTACT | 12488 |
rs47660043 | snp | A/G | | | intron-variant | Cd2ap | Mm_Celera | 17:42862308 | CTCCGCCTCCCGAGC[A/G]CTGGAATTAAAGGTG | 12488 |
rs47678613 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Cd2ap | Mm_Celera | 17:42841996 | TCTTCGTAACTGCCA[A/C]TCACTTCATCTCGCA | 12488 |
rs47705481 | snp | A/C | | | intron-variant | Cd2ap | Mm_Celera | 17:42813841 | GAACAGCATTCTGGA[A/C]GCAAAGGCAGGTGGA | 12488 |
rs47713075 | snp | A/G | 0.132653 | 0.220748 | utr-variant-3-prime, intron-variant | Cd2ap | Mm_Celera | 17:42794205 | AGCCAAACTGCAAAG[A/G]AAAACTTAGTATACA | 12488 |
rs47753704 | snp | A/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42843144 | ATGCCTGATACTGAT[A/T]AACCTAGTACTCACT | 12488 |
rs47754276 | snp | A/G | | | intron-variant | Cd2ap | Mm_Celera | 17:42843115 | GCCCATTTAGCGAGA[A/G]AGATAGATACCATAT | 12488 |
rs47758282 | snp | A/T | | | intron-variant | Cd2ap | GRCm38.p3 | 17:42876105 | TTTAAACCAATCTGT[A/T]CCAAGCCACCGAGTA | 12488 |
rs47762698 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Cd2ap | Mm_Celera | 17:42841762 | CGGAATATCACAATT[C/T]CTGGAGCACAAAGGA | 12488 |
rs47793621 | snp | A/G | | | intron-variant | Cd2ap | Mm_Celera | 17:42836597 | CTAGGAAGTGGGCTA[A/G]CAGAGTGAAACCCTG | 12488 |
rs47802244 | snp | A/C | | | intron-variant | Cd2ap | GRCm38.p3 | 17:42771814 | AAACATAAAGAATGA[A/C]ATGCCCATGAACATA | 12488 |
rs47807509 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Cd2ap | Mm_Celera | 17:42796393 | ATAAATTGAACAACA[C/T]AAAATACCTTTAGCA | 12488 |
rs47812676 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Cd2ap | Mm_Celera | 17:42752309 | GCCAGCTCTTTATTA[C/T]GCAAAAAGTCATACT | 12488 |
rs47814441 | snp | C/T | 0.124444 | 0.216185 | intron-variant, downstream-variant-500B | Cd2ap | Mm_Celera | 17:42808654 | AGTTTTAAAATTGGG[C/T]ATGGCTCTAAGCCTG | 12488 |
rs47841963 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Cd2ap | Mm_Celera | 17:42823664 | ATGCAGAAAAAACAG[C/G]GCTCACTCATTGAGG | 12488 |
rs47844370 | snp | C/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42850603 | TAGCAGAAACGGAAA[C/T]GGTACCACTACTTTC | 12488 |
rs47883266 | snp | A/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42850719 | CACTACTTTCCAAAA[A/T]AACTGACAGTGTCTT | 12488 |
rs47887458 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Cd2ap | Mm_Celera | 17:42813509 | AAGACAGAGCAAAAA[C/T]GTGGCACACCACCAA | 12488 |
rs47888462 | snp | A/G | | | intron-variant | Cd2ap | Mm_Celera | 17:42849441 | ATATTAGCAGATTTC[A/G]ATTTCTCTGGGGATG | 12488 |
rs47911419 | snp | C/G/T | | | intron-variant, upstream-variant-2KB | Cd2ap | GRCm38.p3 | 17:42830547 | AGCTCTTTTCCAAAA[C/G/T]GAAAAGACCCTTTGG | 12488 |
rs47921776 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Cd2ap | Mm_Celera | 17:42816657 | TGTTTTTCATATTGC[C/T]AGCTGGAAAAACGAG | 12488 |
rs47939487 | snp | A/G | | | intron-variant | Cd2ap | Mm_Celera | 17:42849381 | GCACTTTTAACCCAT[A/G]AGCCTTCACAATAGT | 12488 |
rs47971570 | snp | A/G | | | intron-variant | Cd2ap | Mm_Celera | 17:42841616 | GATAAAAAATTAAAA[A/G]AAAAAAAGATACAGC | 12488 |
rs47974951 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Cd2ap | Mm_Celera | 17:42752516 | ATCCTCATAGTCTTG[A/G]AGGCAGAGCCAATGA | 12488 |
rs47992127 | snp | C/T | | | upstream-variant-2KB | Cd2ap | GRCm38.p3 | 17:42876909 | TGAGCCCCGGTTACC[C/T]CACTTTCTTTTTTCT | 12488 |
rs48009026 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Cd2ap | Mm_Celera | 17:42755031 | TCCCATGTTCAGTTC[C/T]TGCAGATTATGCCAG | 12488 |
rs48017005 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Cd2ap | Mm_Celera | 17:42817080 | TGTACACATAGTTCA[A/G]ATCCCTAGTCCAGGA | 12488 |
rs48030686 | snp | A/C | | | intron-variant | Cd2ap | Mm_Celera | 17:42781574 | GTGCTTCTTCTTGCA[A/C]TGTCTTGGTACCAGA | 12488 |
rs48033414 | snp | C/G/T | | | intron-variant | Cd2ap | GRCm38.p3 | 17:42875482 | CTGGGGGCGGGGGGG[C/G/T]GGGGGAGAAACATAC | 12488 |
rs48065818 | snp | C/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42874858 | TTGTTTAGCACCTGG[C/T]CCAACAGTATACAAG | 12488 |
rs48082672 | snp | C/T | 0.32 | 0.24 | intron-variant | Cd2ap | Mm_Celera | 17:42833234 | CCTCTGATATTCATA[C/T]CTGTATCGAACCTTA | 12488 |
rs48092157 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Cd2ap | GRCm38.p3 | 17:42838216 | TAAAGCAATTTCAGC[A/G]TTGCACCCCTACACC | 12488 |
rs48096201 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Cd2ap | Mm_Celera | 17:42752318 | TTATTACGCAAAAAG[C/T]CATACTCCTTACTCA | 12488 |
rs48130523 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Cd2ap | Mm_Celera | 17:42756451 | TGGGTTTACATATGA[C/T]CATCAAGCTCACTTT | 12488 |
rs48142848 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Cd2ap | Mm_Celera | 17:42811230 | AGAAGCATTTCAATG[A/T]CTAGTAGCTGCAGGC | 12488 |
rs48167448 | snp | G/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42846484 | CTGAGTTCATGACCA[G/T]CCTGGTCTACATTCT | 12488 |
rs48194982 | snp | A/G | 0.231111 | 0.249285 | intron-variant, downstream-variant-500B | Cd2ap | Mm_Celera | 17:42808516 | ATGTGCTCTGTGACT[A/G]TGGTCTCAAGGCAAC | 12488 |
rs48215733 | snp | A/G | | | intron-variant | Cd2ap | Mm_Celera | 17:42843332 | TAGAGAAAAACCACA[A/G]CCAATCAAAATGCAG | 12488 |
rs48219530 | snp | G/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42835195 | TTGTCTATTTCTTTA[G/T]TGTGTTCACTTTACG | 12488 |
rs48224278 | snp | A/G | | | intron-variant | Cd2ap | Mm_Celera | 17:42833250 | CTGTATCGAACCTTA[A/G]AAGCTAGTCCCCAAA | 12488 |
rs48248304 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Cd2ap | Mm_Celera | 17:42826518 | ATGGGAGAGAACTGC[A/G]AGAGAAACCAAGAGA | 12488 |
rs48282556 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Cd2ap | Mm_Celera | 17:42790164 | ACATAACAGAAATTA[C/T]GCAACTATAGGGAGA | 12488 |
rs48320156 | snp | C/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42832378 | TGAACTCAGGATCTT[C/T]GGAAGAGCAGTTGGT | 12488 |
rs48356873 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Cd2ap | Mm_Celera | 17:42751871 | AGAACCTGCCACTAA[C/T]GCTAACCCACTTGTT | 12488 |
rs48357002 | snp | A/G | 0.231111 | 0.249285 | intron-variant, utr-variant-5-prime | Cd2ap | Mm_Celera | 17:42828956 | GACGCTGGGGACAGA[A/G]ACCTCCAAAGAAGTG | 12488 |
rs48361860 | snp | A/C | | | intron-variant, utr-variant-5-prime | Cd2ap | Mm_Celera | 17:42828851 | ACACACAGGCACGCA[A/C]ACACATGAAACTATT | 12488 |
rs48369825 | snp | C/T | | | intron-variant, upstream-variant-2KB | Cd2ap | Mm_Celera | 17:42830598 | ATTTAGTATGTCTTA[C/T]ACAGAATACCAAGTT | 12488 |
rs48370269 | snp | A/G | 0.244898 | 0.249948 | intron-variant, upstream-variant-2KB | Cd2ap | GRCm38.p3 | 17:42830788 | TCTTTTTCTCACCTT[A/G]GTTATCCCAGTATCA | 12488 |
rs48393888 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Cd2ap | Mm_Celera | 17:42751573 | ATAAAGATCTCACTG[C/T]CAATGGATACGCAGA | 12488 |
rs48398538 | snp | C/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42848901 | TATTAGCAGTGAGAC[C/T]GGAGATCACTACTGA | 12488 |
rs48407027 | snp | C/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42848326 | TTTTGTAAGGCATGC[C/T]TTCTTTATGGCCTCC | 12488 |
rs48424869 | snp | A/G | | | intron-variant | Cd2ap | GRCm38.p3 | 17:42869195 | GTAGCACTGCCCTCA[A/G]TGGGCTAAGTCCTCT | 12488 |
rs48439236 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Cd2ap | Mm_Celera | 17:42827516 | CAAGTGAGGCTTATC[A/C]ATCTCGTTTTTACAT | 12488 |
rs48467406 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Cd2ap | Mm_Celera | 17:42753994 | TTTCTCCACCTAGGA[A/G]CCAGCAGCCTCAGCA | 12488 |
rs48485358 | snp | C/T | 0.124444 | 0.216185 | synonymous-codon, nc-transcript-variant | Cd2ap | GRCm38.p3 | 17:42816462 | AGGGACTGGCTTTTC[C/T]GGCCGCTTTGGGTAC | 12488 |
rs48495581 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Cd2ap | Mm_Celera | 17:42816855 | CTTCGCTTGCTATTA[A/G]GAGTGATAACACTAT | 12488 |
rs48502909 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Cd2ap | Mm_Celera | 17:42832819 | TAAATAAGACAAGAA[A/G]CTATCAGAATATTCC | 12488 |
rs48518772 | snp | A/C | 0.32 | 0.24 | upstream-variant-2KB, intron-variant | Gpr111, Cd2ap | Mm_Celera | 17:42751100 | ACTACACAGGTCAAC[A/C]AAAAAGCCCGTAACC | 12488 |
rs48520169 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Cd2ap | Mm_Celera | 17:42753261 | GACATGCTATTGTGT[A/G]ACACTATTCCGGAAA | 12488 |
rs48535333 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Cd2ap | Mm_Celera | 17:42828015 | AAATACTCACTTTAA[C/T]TTCTCCCAGGTTTAA | 12488 |
rs48539582 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Cd2ap | Mm_Celera | 17:42823802 | TGCTTCACATAGGCT[A/G]GAACTGAAGATGACA | 12488 |
rs48543065 | snp | G/T | 0.244898 | 0.249948 | intron-variant, upstream-variant-2KB | Cd2ap | Mm_Celera | 17:42830409 | TGGTGATAGAACATT[G/T]AAGAGGTGGCCCCAC | 12488 |
rs48558385 | snp | A/G | | | intron-variant | Cd2ap | Mm_Celera | 17:42791834 | TTTGTTGCAAGGACC[A/G]TGATATAGCTGTCTC | 12488 |
rs48559922 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Cd2ap | Mm_Celera | 17:42824794 | TAAACACTAGTATAA[C/T]GTTTTCCTAGAACAA | 12488 |
rs48569788 | snp | C/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42835759 | ACTTTTCTTGCTGTC[C/T]TGGAACTCATTAAGT | 12488 |
rs48588899 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Cd2ap | Mm_Celera | 17:42828184 | TCAAAGTATCCCTCA[C/T]AGTGCAAGAAGCTAT | 12488 |
rs48603883 | snp | C/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42849037 | AGAGTAAAGGGAGTA[C/T]AATTTCCTGGAGCTT | 12488 |
rs48618103 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Cd2ap | Mm_Celera | 17:42797950 | GAATTCCTCTTCAAG[C/T]AAATGGCGCTTCCAG | 12488 |
rs48639273 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Cd2ap | Mm_Celera | 17:42753040 | ATGCTCAAATGGAAA[G/T]ATATGAGGTCTTTAG | 12488 |
rs48640975 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Cd2ap | Mm_Celera | 17:42754389 | GTCAATGTTTTTGAA[A/T]TTTTTTAAAGGTAAA | 12488 |
rs48654592 | snp | C/T | 0.32 | 0.24 | intron-variant | Cd2ap | Mm_Celera | 17:42812370 | ATACTGGTCAGGGAA[C/T]TGAAATTACTCCATG | 12488 |
rs48665942 | snp | A/G | 0.35503 | 0.226867 | intron-variant | Cd2ap | Mm_Celera | 17:42803367 | GTACCAGTCTGTACC[A/G]TCTACTTATTCCCCT | 12488 |
rs48672402 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Cd2ap | Mm_Celera | 17:42831421 | TCTCCAGCTGTACTC[G/T]CCACCCTACAACCAA | 12488 |
rs48676267 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Cd2ap | Mm_Celera | 17:42810959 | ACACGTACACTTTCA[A/G]CAGAATTACACAGCT | 12488 |
rs48677274 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Cd2ap | Mm_Celera | 17:42831550 | TACCACATTCAACTA[C/T]TTAATGGCAATCACT | 12488 |
rs48682374 | snp | A/C | | | intron-variant | Cd2ap | Mm_Celera | 17:42836838 | TGATGAACTGGGTAT[A/C]CTGTCCATGCCTACA | 12488 |
rs48686788 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Cd2ap | Mm_Celera | 17:42807678 | AATAAGAAAATTAAA[C/T]GGTATAAAAATCAAT | 12488 |
rs48695703 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Cd2ap | Mm_Celera | 17:42752386 | TTTTTGAGCAGGTGA[A/G]GAAATGACAAACATT | 12488 |
rs48715075 | snp | C/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42850301 | ATTTACAAAGATGTA[C/T]CTAATGAACATCTTT | 12488 |
rs48719416 | snp | G/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42852794 | ATAAGATTTCCCACA[G/T]AAGGCTACCACCCTT | 12488 |
rs48747049 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Cd2ap | Mm_Celera | 17:42833366 | AGAAAATAAAGGAAC[A/G]AGTCTAAAGACAAGA | 12488 |
rs48751759 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Cd2ap | Mm_Celera | 17:42815716 | CATTACATAACAGTC[A/G]AGACATAATGAAGTA | 12488 |
rs48788514 | snp | A/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42835973 | CTTTGCTGAAACAGG[A/T]AAGTTGGGAGATTAT | 12488 |
rs48796171 | snp | A/G | | | intron-variant | Cd2ap | Mm_Celera | 17:42849558 | ATAGCAGTGGCCCTT[A/G]GTGAATACAGAATAT | 12488 |
rs48796967 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Cd2ap | Mm_Celera | 17:42812605 | AAGGACAAAACGTCC[A/G]CAGTAACTTCCCATC | 12488 |
rs48802134 | snp | C/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42848876 | CTTGCCATTAGAAGA[C/T]AACTACAAATATTAG | 12488 |
rs48817728 | snp | C/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42857918 | CTAGAAAGAATTTAC[C/T]GAGTAGGACAAAAGG | 12488 |
rs48836640 | snp | C/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42850920 | CAGCACTTCACAGAA[C/T]GAAATAGGCAGGTTG | 12488 |
rs48838911 | snp | C/T | | | missense | Cd2ap | GRCm38.p3 | 17:42805235 | TCGTCCACGGAATTT[C/T]TTTTCCCATCATCTG | 12488 |
rs48864445 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Cd2ap | Mm_Celera | 17:42831327 | CATGTCTCTCCATCA[A/C]CACAGCATTCTTCTA | 12488 |
rs48868976 | snp | A/G | | | intron-variant | Cd2ap | Mm_Celera | 17:42850240 | GGGGGTGGAGGGAAC[A/G]GGAATGAATACACCA | 12488 |
rs48889337 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Cd2ap | Mm_Celera | 17:42812022 | GAATTTATCACAGAG[A/G]GAAAAAAATCAAAAG | 12488 |
rs48896558 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Cd2ap | Mm_Celera | 17:42752673 | GGAACATAGATAACC[A/G]AACGCATCATGCAGA | 12488 |
rs48910196 | snp | G/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42848891 | TAACTACAAATATTA[G/T]CAGTGAGACTGGAGA | 12488 |
rs48943132 | snp | C/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42807203 | ATTCTGCCACTAAGT[C/T]CAATACATACTGAAC | 12488 |
rs48952107 | snp | A/C | 0.142012 | 0.225474 | intron-variant | Cd2ap | Mm_Celera | 17:42812811 | GGCAACTATCAGTAC[A/C]AGGGATTTGTCTGTT | 12488 |
rs48961172 | snp | A/G | 0.32 | 0.24 | intron-variant | Cd2ap | Mm_Celera | 17:42798191 | GGAGCTGACCAGGAC[A/G]CAGGAAGGCAAAAGC | 12488 |
rs48974050 | snp | A/G | 0.124444 | 0.216185 | upstream-variant-2KB, intron-variant | Gpr111, Cd2ap | Mm_Celera | 17:42750502 | CCCCAGAAGCTTACC[A/G]TCCTCTCACTAGGTC | 12488 |
rs48980719 | snp | A/T | 0.391111 | 0.206368 | intron-variant | Cd2ap | Mm_Celera | 17:42751592 | TGGATACGCAGAAAG[A/T]GGAGAGCAGAACTTC | 12488 |
rs48982139 | snp | C/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42848621 | TGTAAGCACTGTATA[C/T]ACATACATAAACATA | 12488 |
rs48988498 | snp | C/G/T | | | intron-variant, upstream-variant-2KB | Cd2ap | GRCm38.p3 | 17:42831081 | TTTCTGAGTTCGAGG[C/G/T]CAGCCTGGTCTACAA | 12488 |
rs49018717 | snp | C/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42872089 | GGCAGGGCGTGGTGG[C/T]GCACGCCTTTAATCC | 12488 |
rs49035823 | snp | C/T | 0.375 | 0.216506 | intron-variant | Cd2ap | Mm_Celera | 17:42809210 | TTGAAGTTCTCACAT[C/T]TTTAAAAATCTATTT | 12488 |
rs49037462 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Cd2ap | Mm_Celera | 17:42756960 | AAGACTAAACAATAG[A/G]CTGCTCTAGTCTAAA | 12488 |
rs49038161 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Cd2ap | Mm_Celera | 17:42812589 | AACTGCCGACGGGCT[A/G]AAGGACAAAACGTCC | 12488 |
rs49055516 | snp | C/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42853181 | CACCATGTTAGTATG[C/T]TGGCTTAGGGAAGGT | 12488 |
rs49060395 | snp | A/G | | | intron-variant | Cd2ap | Mm_Celera | 17:42791842 | AAGGACCGTGATATA[A/G]CTGTCTCTTGTGAGA | 12488 |
rs49075837 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Cd2ap | Mm_Celera | 17:42813253 | TGGCCTCAAGGTACA[C/T]AAGTAGCTGGCAAGG | 12488 |
rs49101152 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Cd2ap | Mm_Celera | 17:42797256 | GTAGAACCACGCAGG[C/T]AAGAACTCTCACAGG | 12488 |
rs49107272 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Cd2ap | Mm_Celera | 17:42833841 | AATTCTTCAAAAGAT[A/G]GATTTGGCTACAGAG | 12488 |
rs49115850 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Cd2ap | Mm_Celera | 17:42807757 | TAAGTACTTCTATTC[C/T]TAAGAGCTACAGAAG | 12488 |
rs49117635 | snp | A/G | | | intron-variant | Cd2ap | GRCm38.p3 | 17:42842509 | TGAGCCAGGCGTGGT[A/G]GTGCACACCTTTAAC | 12488 |
rs49123940 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Cd2ap | Mm_Celera | 17:42805138 | TTTAGGGAACGCATC[A/G]AAGGAATTAAGAGTT | 12488 |
rs49126771 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Cd2ap | Mm_Celera | 17:42841638 | AGATACAGCTCTATG[C/G]TATTCCACTCAACTA | 12488 |
rs49128353 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Cd2ap | Mm_Celera | 17:42754897 | GATAACTACAAAGTC[C/T]ACTTGAACAAACATC | 12488 |
rs49135083 | snp | C/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42841480 | CACTGACTGCTCTTC[C/T]GAAGGTCCTGAGTTC | 12488 |
rs49157185 | snp | A/C | | | intron-variant | Cd2ap | Mm_Celera | 17:42850544 | ACATTGATAACACCA[A/C]ATATGGGTAAAGATA | 12488 |
rs49202997 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Cd2ap | Mm_Celera | 17:42841416 | AAAGCACAGAAACTG[C/T]ACAAAAAGATACAGC | 12488 |
rs49210631 | snp | A/G | 0.132653 | 0.220748 | intron-variant, upstream-variant-2KB | Cd2ap | Mm_Celera | 17:42829711 | GATCACATCTGTGAA[A/G]CATTTTCTGATGGCT | 12488 |
rs49211787 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Cd2ap | Mm_Celera | 17:42798465 | CAGAATCAACAGAAA[C/T]TTAGGCAACTATTAC | 12488 |
rs49231806 | snp | C/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42850875 | AACTAAGATACCCAT[C/T]GGGGAAACATACTGG | 12488 |
rs49268886 | snp | A/G | | | intron-variant | Cd2ap | Mm_Celera | 17:42848609 | TTTTTTGGCCTCTGT[A/G]AGCACTGTATATACA | 12488 |
rs49296453 | snp | C/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42841531 | TGGCTCACAACCATC[C/T]GTAATGAGATCTGAT | 12488 |
rs49335238 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Cd2ap | Mm_Celera | 17:42753923 | GAATGTTTCTTAAAC[A/G]TCCTTAATGCTTAAA | 12488 |
rs49359663 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Cd2ap | Mm_Celera | 17:42817194 | ATGAAAGTCTAAAAA[A/G]TTTCCTGCTAAACAG | 12488 |
rs49371592 | snp | A/G | | | intron-variant | Cd2ap | Mm_Celera | 17:42798355 | TGTCACGGAGCTGGA[A/G]CTGCAGCTCCACGTC | 12488 |
rs49372495 | snp | C/T | 0.32 | 0.24 | intron-variant | Cd2ap | Mm_Celera | 17:42752436 | GCTCTGCCAGCCCTG[C/T]AATTGACCATTGAGA | 12488 |
rs49432964 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Cd2ap | Mm_Celera | 17:42808157 | TACTGCTGTGGACAA[A/G]ATGTCACATAACATC | 12488 |
rs49452165 | snp | C/T | | | upstream-variant-2KB | Cd2ap | Mm_Celera | 17:42877989 | CATAGCCCTTATCCT[C/T]CGTGACTTTGCATTC | 12488 |
rs49474232 | snp | A/G | | | upstream-variant-2KB | Cd2ap | GRCm38.p3 | 17:42876720 | GGCCACGCCCCCTGC[A/G]GCCCCCGCGCGCGCC | 12488 |
rs49480732 | snp | G/T | 0.244898 | 0.249948 | intron-variant | Cd2ap | GRCm38.p3 | 17:42813788 | GAGTGTATAGAAAAC[G/T]TGAGGGCTTGGAAAG | 12488 |
rs49480992 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Cd2ap | Mm_Celera | 17:42755224 | CCCTATGTGTTTACA[C/T]TGGAAGTGGCTCCTC | 12488 |
rs49501961 | snp | A/G | | | intron-variant | Cd2ap | Mm_Celera | 17:42832712 | AGAAATCAAATAAAA[A/G]ACAAATGAAATTAAA | 12488 |
rs49502585 | snp | A/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42804654 | TAACTTTCAGAGCTG[A/T]GGACATGGGTCAATG | 12488 |
rs49512195 | snp | A/G | 0.124444 | 0.216185 | synonymous-codon, nc-transcript-variant | Cd2ap | GRCm38.p3 | 17:42826300 | AATCTTGCCATCAAC[A/G]TCTGGTTTTGTTACC | 12488 |
rs49516398 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Cd2ap | Mm_Celera | 17:42751474 | AAATGCCTTCCCGGT[A/G]TCTACATAAGGCATT | 12488 |
rs49561978 | snp | C/G | | | intron-variant | Cd2ap | Mm_Celera | 17:42832802 | GATTAATAAAAGAAT[C/G]TTAAATAAGACAAGA | 12488 |
rs49579668 | snp | A/T | 0.132653 | 0.220748 | intron-variant | Cd2ap | Mm_Celera | 17:42835908 | TACAAGTCATGAGGT[A/T]ACTGCTAGTAAAAGA | 12488 |
rs49601516 | snp | A/G | | | intron-variant | Cd2ap | Mm_Celera | 17:42846147 | TCTTCCACTGTATGA[A/G]ACGACAGTGGGATTA | 12488 |
rs49607699 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Cd2ap | Mm_Celera | 17:42753962 | GACTGGGAAGGAGTC[C/T]AGTAAATCTTGGTCC | 12488 |
rs49611278 | snp | A/G | 0.32 | 0.24 | intron-variant | Cd2ap | Mm_Celera | 17:42809924 | TTTCTTTAGACCTAA[A/G]CATACTCATCTTTAT | 12488 |
rs49647830 | snp | G/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42850641 | ACTGACAGTGTCTTA[G/T]TAAACCAACATTTGT | 12488 |
rs49663047 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Cd2ap | Mm_Celera | 17:42806835 | CCAAATGGATGGTTC[A/G]TATAGTGAGGCATCT | 12488 |
rs49712715 | snp | G/T | 0.32 | 0.24 | intron-variant | Cd2ap | Mm_Celera | 17:42809894 | ACTTATATGTTCAAA[G/T]TCAGTGATCTGATGT | 12488 |
rs49740483 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Cd2ap | Mm_Celera | 17:42840821 | TTGCTAAACTGAGAG[A/G]AACTGTGATAGTATG | 12488 |
rs49743306 | snp | A/G | | | intron-variant | Cd2ap | Mm_Celera | 17:42861353 | TGGTTAGATCATCAG[A/G]GAGTGCCACTACTTA | 12488 |
rs49749930 | snp | C/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42853467 | AAGTGCAGATGCCTG[C/T]GAAATCTGACAGATC | 12488 |
rs49755981 | snp | A/G | | | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | Cd2ap | GRCm38.p3 | 17:42876649 | CCACGGGCCCAGTGT[A/G]AAGAGAGTCGGGACC | 12488 |
rs49758390 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Cd2ap | Mm_Celera | 17:42837185 | CAAACTCAGGCCACT[A/G]CATGTCAGGCATATA | 12488 |
rs49761193 | snp | A/G | 0.32 | 0.24 | intron-variant, downstream-variant-500B | Gpr111, Cd2ap | Mm_Celera | 17:42748990 | CCATGGCCTGATGCC[A/G]TCTGTTACTGAGCAA | 12488 |
rs49761320 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Cd2ap | Mm_Celera | 17:42817523 | ATTCCCTTACAGCTT[A/G]TGAAAAACGGCAATC | 12488 |
rs49762377 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Cd2ap | Mm_Celera | 17:42831257 | CTCCACAGTCCACCA[C/T]CATTAGGTCCTATGT | 12488 |
rs49777393 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Cd2ap | Mm_Celera | 17:42789979 | AAGTGAACAGAAGCT[C/T]ATTATAGGCTGGGAT | 12488 |
rs49782160 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Cd2ap | Mm_Celera | 17:42804729 | ACTACACAAACAAGA[A/G]CTTTCAGAGCTAACG | 12488 |
rs49794381 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Cd2ap | Mm_Celera | 17:42831211 | ACCCAAAGACTACCT[A/G]GTAATCTCTGGGCCC | 12488 |
rs49794646 | snp | C/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42849376 | AAGAAGCACTTTTAA[C/T]CCATGAGCCTTCACA | 12488 |
rs49797356 | snp | C/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42850256 | GGAATGAATACACCA[C/T]CAAGGAGAAAAAAAT | 12488 |
rs49823937 | snp | C/T | | | upstream-variant-2KB | Cd2ap | Mm_Celera | 17:42878692 | TGTGACAAGGACCAA[C/T]ATAGTACCGAAGTGT | 12488 |
rs49827937 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Cd2ap | Mm_Celera | 17:42804689 | TTGAGTGCATTAACA[C/T]CACACTCTGGGCTTG | 12488 |
rs49838899 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Cd2ap | Mm_Celera | 17:42789603 | TATGTCTGCGGGGGC[A/G]GTCGTAAGAGATTTA | 12488 |
rs49839403 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Cd2ap | Mm_Celera | 17:42807896 | AACTAACCAAATCTT[A/G]GGCCACAATAGATCT | 12488 |
rs49874297 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Cd2ap | Mm_Celera | 17:42841954 | ACATATATCATTAAC[A/G]CCTCATATTTACATT | 12488 |
rs49901259 | snp | A/C | | | intron-variant | Cd2ap | Mm_Celera | 17:42872245 | AACAAAACAAAAAAA[A/C]AAAAAAGGCTCAACT | 12488 |
rs49908564 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Cd2ap | Mm_Celera | 17:42833499 | AATATAAAGTATCCT[A/G]ATTTGATGGTGATAA | 12488 |
rs49923189 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Cd2ap | Mm_Celera | 17:42813555 | GTGAAAAGAACCAAG[A/G]ACAGTTGCTTACAAG | 12488 |
rs49960496 | snp | A/G | 0.32 | 0.24 | intron-variant | Cd2ap | Mm_Celera | 17:42810637 | AAAGCCTTGATATGT[A/G]ATCTACAATTAGTTA | 12488 |
rs49974266 | snp | A/G | | | intron-variant | Cd2ap | Mm_Celera | 17:42832421 | TGAGTCATCTCTCCA[A/G]CCCCAATTTCCTCAC | 12488 |
rs50009821 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Cd2ap | Mm_Celera | 17:42814199 | CTTTAAAACCAAATA[C/G]AGTGATACAAAGTAA | 12488 |
rs50043697 | snp | A/G | | | intron-variant | Cd2ap | Mm_Celera | 17:42835523 | GATTGCTTAATTTCC[A/G]TAAGTTAAAAAACAT | 12488 |
rs50046259 | snp | A/G | | | upstream-variant-2KB | Cd2ap | Mm_Celera | 17:42877857 | ATTTCATTTGCACAA[A/G]TAAACAAGATGTCAG | 12488 |
rs50051447 | snp | C/T | | | intron-variant, utr-variant-5-prime | Cd2ap | Mm_Celera | 17:42828914 | TTTCCTCTGGAGTAA[C/T]TGCTTAGTTTGTATC | 12488 |
rs50061201 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Cd2ap | Mm_Celera | 17:42836803 | AAGGGTGGTAAAGAT[C/G]ACTCATTCACTCATA | 12488 |
rs50066128 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Cd2ap | Mm_Celera | 17:42755746 | GTGCTACACCATCCA[C/T]AGCAATGCATAGAGA | 12488 |
rs50071400 | snp | A/G | | | missense | Cd2ap | GRCm38.p3 | 17:42805335 | GTGTTGAAAGAGATG[A/G]CTGAAAAATATTTTT | 12488 |
rs50081781 | snp | A/G | 0.32 | 0.24 | intron-variant | Cd2ap | Mm_Celera | 17:42806010 | CACTACAGTGGGTGT[A/G]GGATCGCTTACAGCC | 12488 |
rs50099648 | snp | A/G | | | upstream-variant-2KB | Cd2ap | Mm_Celera | 17:42878651 | ATAAATAACTGCATT[A/G]AAATATTTTCCTGTT | 12488 |
rs50114549 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Cd2ap | Mm_Celera | 17:42832784 | AGGCATCAATACTGA[C/T]GTGATTAATAAAAGA | 12488 |
rs50125413 | snp | A/G | | | intron-variant, upstream-variant-2KB | Cd2ap | Mm_Celera | 17:42831011 | ATCCCAAATATAGCC[A/G]GGCATGGTGGCGCAC | 12488 |
rs50154496 | snp | A/T | 0.244898 | 0.249948 | intron-variant | Cd2ap | Mm_Celera | 17:42842419 | GCATTTCTAAAAATA[A/T]CCACTTATTTCTCAA | 12488 |
rs50161782 | snp | C/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42837152 | TCAAGACACACAAGT[C/T]AACAAGCTTCACACA | 12488 |
rs50189701 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Cd2ap | Mm_Celera | 17:42815795 | CTCAGCTCAGTCAGG[A/G]CTGTGTTCTGCCCAC | 12488 |
rs50211688 | snp | A/G | | | intron-variant | Cd2ap | Mm_Celera | 17:42866798 | GACCACATGTGCAGT[A/G]CACTGCGGTGTTTAT | 12488 |
rs50213182 | snp | G/T | 0.142012 | 0.225474 | intron-variant | Cd2ap | Mm_Celera | 17:42803690 | AAAGGAGTGCACTTG[G/T]TATCAATGTGTAAAA | 12488 |
rs50215588 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Cd2ap | Mm_Celera | 17:42753228 | GTTCACACCTGGTCT[C/T]CTTTGTTTGAAAGCT | 12488 |
rs50228879 | snp | A/C/G | | | intron-variant | Cd2ap | GRCm38.p3 | 17:42866805 | TGTGCAGTACACTGC[A/C/G]GTGTTTATTATACAT | 12488 |
rs50230858 | snp | A/G | | | intron-variant | Cd2ap | Mm_Celera | 17:42864986 | TTCTTGGGAGGCGAG[A/G]CGTAATAACACCCAG | 12488 |
rs50316911 | snp | A/G | | | utr-variant-5-prime, nc-transcript-variant | Cd2ap | GRCm38.p3 | 17:42876373 | CTGTGCACCGGCTCA[A/G]GCGCGGCGGGGAAGC | 12488 |
rs50329996 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Cd2ap | Mm_Celera | 17:42756544 | GGTGTGGTGTGATAG[C/T]TTACCGTGTTAGCAG | 12488 |
rs50351847 | snp | C/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42841455 | GGAAAGATGGCTCAG[C/T]GGTTAAGAGCACTGA | 12488 |
rs50364765 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Cd2ap | Mm_Celera | 17:42835866 | CCAACGTTTGATAAG[C/T]AATTCATGGAACAGG | 12488 |
rs50379537 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Cd2ap | Mm_Celera | 17:42798321 | ATCTAGTGCTTCACA[C/T]GCTGTAAAGACTCGG | 12488 |
rs50380238 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Cd2ap | Mm_Celera | 17:42751717 | ATGGCCATGTGGCAG[A/G]ACGCAGGCCAGAATG | 12488 |
rs50381788 | snp | A/G | | | intron-variant | Cd2ap | Mm_Celera | 17:42818875 | CCCTGTCTCGGGGGG[A/G]AAAAAAAAACAGACA | 12488 |
rs50384807 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Cd2ap | Mm_Celera | 17:42815092 | AGATGTCTGTGCTTC[C/T]AGCTCTCCACCTTCC | 12488 |
rs50416703 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Cd2ap | Mm_Celera | 17:42817150 | GGCCCAGCACTGAAC[G/T]ATTATTTGTCTTTGA | 12488 |
rs50473803 | snp | C/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42858015 | GAGATGGCTCAGAGG[C/T]TAAGAGCACTGATTG | 12488 |
rs50477148 | snp | C/T | 0.18 | 0.24 | intron-variant | Cd2ap | Mm_Celera | 17:42804872 | CCTCTAAGAGTTAAG[C/T]ATGAGGATCTAGATC | 12488 |
rs50494344 | snp | A/G | | | intron-variant, upstream-variant-2KB | Cd2ap | Mm_Celera | 17:42831015 | CAAATATAGCCAGGC[A/G]TGGTGGCGCACGCCT | 12488 |
rs50508432 | snp | G/T | 0.197531 | 0.244432 | intron-variant | Cd2ap | Mm_Celera | 17:42810869 | TATTTTAAATTATAA[G/T]CAAGAAAGGTTTTTG | 12488 |
rs50520032 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Cd2ap | Mm_Celera | 17:42816918 | TAATAGTGCAAAAAT[A/G]CTTAAAGAACTGTAT | 12488 |
rs50523474 | snp | G/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42836914 | GGTCTGAATGAACTA[G/T]GAGATCCTATCTCTA | 12488 |
rs50543377 | snp | C/T | 0.132653 | 0.220748 | intron-variant, upstream-variant-2KB | Cd2ap | Mm_Celera | 17:42830481 | TAGGATTTGTAAGAA[C/T]AGATTAGTTCGTCAA | 12488 |
rs50585983 | snp | C/G | | | intron-variant | Cd2ap | Mm_Celera | 17:42798367 | GGAACTGCAGCTCCA[C/G]GTCTGAATGACTCCC | 12488 |
rs50610244 | snp | G/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42832417 | CCACTGAGTCATCTC[G/T]CCAGCCCCAATTTCC | 12488 |
rs50619366 | snp | A/G | | | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | Cd2ap | GRCm38.p3 | 17:42876456 | GCAGCCCCGGCAGGC[A/G]GGGGTGGGAGGGGGG | 12488 |
rs50637432 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Cd2ap | Mm_Celera | 17:42811771 | TACTAGGAATCACAA[C/T]ACCGTTTTGATATGG | 12488 |
rs50678061 | snp | A/G | | | intron-variant | Cd2ap | Mm_Celera | 17:42841434 | AAAAAGATACAGCTC[A/G]GGGCTGGAAAGATGG | 12488 |
rs50691962 | snp | C/T | 0.124444 | 0.216185 | upstream-variant-2KB, intron-variant | Gpr111, Cd2ap | Mm_Celera | 17:42750538 | TCTTAAGTTCTACTA[C/T]CTTCCCATGGTGCCA | 12488 |
rs50692023 | snp | A/C | 0.32 | 0.24 | intron-variant | Cd2ap | Mm_Celera | 17:42814868 | TCATTGGTGATTGAG[A/C]GTACTGATGTGTCTG | 12488 |
rs50708379 | snp | A/G | | | intron-variant | Cd2ap | GRCm38.p3 | 17:42876116 | CTGTACCAAGCCACC[A/G]AGTAGCAGAGCTGCA | 12488 |
rs50713819 | snp | A/G | | | intron-variant | Cd2ap | Mm_Celera | 17:42781670 | GAAGACAGGAGCAGA[A/G]AAACAGAAGATAGCC | 12488 |
rs50716782 | snp | C/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42842110 | AATGACTCTGGGCTG[C/T]ATAACCTAAGTTTGA | 12488 |
rs50728142 | snp | A/C | 0.152778 | 0.230321 | intron-variant | Cd2ap | Mm_Celera | 17:42823233 | GTGCTGGAGCCACTG[A/C]TTTTTTCTGCCCTTG | 12488 |
rs50745395 | snp | A/C | | | intron-variant | Cd2ap | Mm_Celera | 17:42857849 | ACCCACAAATAAAGA[A/C]GCATCCCAACTTGGA | 12488 |
rs50758193 | snp | C/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42850597 | CATCCCTAGCAGAAA[C/T]GGAAACGGTACCACT | 12488 |
rs50768601 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Cd2ap | Mm_Celera | 17:42790535 | CACACACTGCCACAA[C/T]GAAATCATTACTTTG | 12488 |
rs50778815 | snp | C/G | | | intron-variant | Cd2ap | Mm_Celera | 17:42835549 | AACATTCAATAAATT[C/G]CTTTCAAATATATAG | 12488 |
rs50787719 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Cd2ap | Mm_Celera | 17:42835968 | CTTGCCTTTGCTGAA[A/G]CAGGAAAGTTGGGAG | 12488 |
rs50797852 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Cd2ap | Mm_Celera | 17:42839782 | CAGCTCTCAGCTCCA[C/T]GCAGGAGGTTCCTGT | 12488 |
rs50799237 | snp | C/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42846149 | TTCCACTGTATGAAA[C/T]GACAGTGGGATTAAA | 12488 |
rs50805418 | snp | A/T | 0.244898 | 0.249948 | intron-variant | Cd2ap | Mm_Celera | 17:42831357 | AGTTTAGACAAATAC[A/T]CTTTCTACCTAAATC | 12488 |
rs50822052 | snp | A/C | | | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | Cd2ap | GRCm38.p3 | 17:42876495 | CGGGGTCCGCGCCTG[A/C]GCACAGGGCGCACTC | 12488 |
rs50855145 | snp | A/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42831760 | TGTCAATCTATATTA[A/T]CGTTGACCTATTTAA | 12488 |
rs50865698 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Cd2ap | Mm_Celera | 17:42833291 | AACAATGCACTGAAT[C/T]CACTCAAGAAAGACC | 12488 |
rs50873661 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Cd2ap | Mm_Celera | 17:42751813 | GTGTCATTATTTATA[C/T]AGCTGGCGTGTCAGT | 12488 |
rs50924717 | snp | C/T | 0.124444 | 0.216185 | upstream-variant-2KB, utr-variant-3-prime | Gpr111, Cd2ap | Mm_Celera | 17:42749146 | AGGACAGGTTGACTT[C/T]TGCTCATAGTTTTAC | 12488 |
rs50927775 | snp | G/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42843067 | GGCACCCATACCTTG[G/T]TGGTAACCAACAGCT | 12488 |
rs50929402 | snp | C/T | 0.32 | 0.24 | intron-variant | Cd2ap | Mm_Celera | 17:42752003 | ATAGGAGAAGTTTGG[C/T]GTTTGGTTTCTTTGA | 12488 |
rs50932681 | snp | G/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42783487 | TCAGCTGTATCTTGG[G/T]GCTACATACTTGCCA | 12488 |
rs50970964 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Cd2ap | Mm_Celera | 17:42755441 | ACAAAAATTCTTAAG[C/T]CATTTGATAAAATAC | 12488 |
rs50987613 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Cd2ap | Mm_Celera | 17:42809274 | ATGTATAGCATTTTA[C/T]ACTTCACACTGTAGA | 12488 |
rs50987777 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Cd2ap | Mm_Celera | 17:42839151 | TTTTCAGACTACTTA[C/T]TGATCAAAGCCTAGG | 12488 |
rs51010250 | snp | A/G | | | intron-variant | Cd2ap | Mm_Celera | 17:42848990 | AGTTAAAGACAAAAG[A/G]ATGTTAATACACATG | 12488 |
rs51018083 | snp | A/G | | | intron-variant | Cd2ap | Mm_Celera | 17:42781745 | GGTACGTAAGGAACT[A/G]TAGAAGGGATGCATT | 12488 |
rs51033800 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Cd2ap | Mm_Celera | 17:42752144 | AAAGACACAGAGATG[C/T]CTATATCGTTTAAAC | 12488 |
rs51075159 | snp | A/G | | | intron-variant | Cd2ap | Mm_Celera | 17:42836606 | GGGCTAACAGAGTGA[A/G]ACCCTGCCTCAAAGG | 12488 |
rs51088040 | snp | A/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42857769 | ACTGAGGCGCTATTG[A/T]CAGCTGATGGCCTCT | 12488 |
rs51091261 | snp | A/G | | | upstream-variant-2KB | Cd2ap | Mm_Celera | 17:42878376 | AGGTCCCCTACAAGA[A/G]CAGCAGGTGCCTTTA | 12488 |
rs51093570 | snp | A/T | 0.124444 | 0.216185 | utr-variant-3-prime, intron-variant | Cd2ap | Mm_Celera | 17:42796303 | TAAGTTCATGAATCA[A/T]TAGGAACACTGGGTC | 12488 |
rs51128463 | snp | A/G | | | upstream-variant-2KB | Cd2ap | Mm_Celera | 17:42877865 | TGCACAAATAAACAA[A/G]ATGTCAGCAGGGTAT | 12488 |
rs51135455 | snp | C/T | | | upstream-variant-2KB | Cd2ap | Mm_Celera | 17:42877742 | GCATCTTTCACTACT[C/T]CTAAAAAGATTGCCA | 12488 |
rs51140333 | snp | C/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42781270 | TCTAAAACAAATGCA[C/T]GTTGTTTTATTCCAT | 12488 |
rs51145555 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Cd2ap | Mm_Celera | 17:42797472 | ACTAACTCTCTGACA[A/T]CAAGGGTAAGTAACA | 12488 |
rs51165263 | snp | C/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42843386 | GATTCATATACAGAA[C/T]CCCGAACCTAAGGCT | 12488 |
rs51235000 | snp | A/G | 0.297521 | 0.245442 | intron-variant, upstream-variant-2KB | Cd2ap | Mm_Celera | 17:42830396 | CGTGTGTTAAGTCTG[A/G]TGATAGAACATTTAA | 12488 |
rs51272161 | snp | C/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42845891 | TTAATAACACAGTAG[C/T]TTTAAGTCAAGAGTT | 12488 |
rs51313405 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Cd2ap | Mm_Celera | 17:42834085 | AAAACTACATTAGCT[A/G]AAACTGACTAAGCAC | 12488 |
rs51343110 | snp | A/G | | | intron-variant | Cd2ap | Mm_Celera | 17:42852903 | TGGACTGTGTGGAAT[A/G]AATGAATATCGTAAT | 12488 |
rs51376172 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Cd2ap | Mm_Celera | 17:42823628 | TTATGTTGCTCCAAG[C/T]TGTAAAAAGTAACAT | 12488 |
rs51379909 | snp | A/G | | | intron-variant, upstream-variant-2KB | Cd2ap | Mm_Celera | 17:42829882 | ACTTTTGGTCTGTAT[A/G]TATTATAGTGAGAGA | 12488 |
rs51385192 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Cd2ap | Mm_Celera | 17:42827249 | ATGGAGGTCAAAGAG[A/G]ACAGTGGATTCCCTG | 12488 |
rs51404346 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Cd2ap | Mm_Celera | 17:42752211 | TTGGGATTTAACCGG[A/G]CTTCCCCATTTTGTC | 12488 |
rs51418393 | snp | A/G | | | intron-variant, upstream-variant-2KB | Cd2ap | Mm_Celera | 17:42830972 | TTGTACCCTCATGTA[A/G]TGACATAAAATACTT | 12488 |
rs51421933 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Cd2ap | Mm_Celera | 17:42831661 | TTGAAGGCCTCAATA[A/G]CATAAATGACTTCTT | 12488 |
rs51439957 | snp | C/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42781720 | ATATAGCATGCTGCA[C/T]TGTGAGGTTGGTACG | 12488 |
rs51450988 | snp | A/C | 0.260355 | 0.249785 | intron-variant | Cd2ap | Mm_Celera | 17:42755123 | TAACTACAATAAATA[A/C]CCGTCACCCATAGAC | 12488 |
rs51479574 | snp | A/G | | | intron-variant | Cd2ap | GRCm38.p3 | 17:42876234 | GCCCCGCTGTCCCGC[A/G]CAAGGACCGACGAGG | 12488 |
rs51480497 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Cd2ap | Mm_Celera | 17:42754221 | ACAAAAGGCGTGTGG[A/G]ATGAGTTTAAGGACA | 12488 |
rs51494889 | snp | G/T | 0.132653 | 0.220748 | intron-variant, utr-variant-5-prime | Cd2ap | Mm_Celera | 17:42829037 | GTTCACTTGACTCCA[G/T]TTTTAAAATGCTGGT | 12488 |
rs51497327 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Cd2ap | Mm_Celera | 17:42833333 | TCTTCAAAAGTCCCA[A/G]TGTCCAGACAAGAAG | 12488 |
rs51514441 | snp | A/T | 0.18 | 0.24 | intron-variant | Cd2ap | Mm_Celera | 17:42817793 | CCACTAGGAGAAAAA[A/T]ACAAAACTTCCTATT | 12488 |
rs51526827 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Cd2ap | Mm_Celera | 17:42797358 | CTTTGTAGGAGGGGC[A/G]ACATCCTCACTGCTC | 12488 |
rs51528832 | snp | C/T | | | intron-variant | Cd2ap | GRCm38.p3 | 17:42876200 | CCAGAGGGCGCAGGG[C/T]AACGGGTCACGGGTT | 12488 |
rs51538983 | snp | C/T | | | intron-variant | Cd2ap | GRCm38.p3 | 17:42833659 | CATGAGAACTCTTTC[C/T]TTTTTTTATGTTTAC | 12488 |
rs51571494 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Cd2ap | Mm_Celera | 17:42825201 | ACCTGAGTTCAAACC[C/T]GGTGACACACAGTGT | 12488 |
rs51582702 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Cd2ap | Mm_Celera | 17:42812536 | AAGAAATCAAGTCTT[C/T]CATAGGTCAGAGCAG | 12488 |
rs51621367 | snp | C/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42781595 | TGGTACCAGAGTGCC[C/T]TAGGGCTGCCCTCCC | 12488 |
rs51638220 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Cd2ap | Mm_Celera | 17:42752877 | ACTTCTGACCCGCTG[C/T]GACATAAAGGTGAGA | 12488 |
rs51648949 | snp | C/T | | | intron-variant | Cd2ap | GRCm38.p3 | 17:42835209 | ATTGTGTTCACTTTA[C/T]GTGTATGGGCATTTG | 12488 |
rs51660177 | snp | C/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42833330 | CACTCTTCAAAAGTC[C/T]CAGTGTCCAGACAAG | 12488 |
rs51681874 | snp | A/T | | | upstream-variant-2KB | Cd2ap | GRCm38.p3 | 17:42876934 | TTTTCTTTCTTTTTT[A/T]TTTATTTTTTTTTTT | 12488 |
rs51682578 | snp | G/T | 0.42 | 0.183303 | intron-variant | Cd2ap | GRCm38.p3 | 17:42834669 | GCCTTGCTTTATAAA[G/T]ATAACATGTTTTAGT | 12488 |
rs51683850 | snp | C/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42852584 | CAAAATTACTATAAA[C/T]CATATTAACAAGCTT | 12488 |
rs51691155 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Cd2ap | Mm_Celera | 17:42823757 | AGAATTGCCAGCGGT[A/G]GACTTAATTAAAGAC | 12488 |
rs51705309 | snp | A/G | 0.32 | 0.24 | upstream-variant-2KB, missense | Gpr111, Cd2ap | Mm_Celera | 17:42749192 | ATCAGTTAGCCCATT[A/G]ATTTTGGGGCCTGTG | 12488 |
rs51709395 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Cd2ap | Mm_Celera | 17:42797822 | TCCATCCTGAGCCTG[C/T]GTGTACTGGTGGTAG | 12488 |
rs51720669 | snp | A/G | 0.32 | 0.24 | intron-variant | Cd2ap | Mm_Celera | 17:42751560 | CTGATTGGCTTTAAT[A/G]AAGATCTCACTGTCA | 12488 |
rs51737444 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Cd2ap | Mm_Celera | 17:42798276 | GAAGATCAAGGGATA[A/C]CACTTGTTTACTCAC | 12488 |
rs51765856 | snp | A/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42872043 | TCTTCTAGCCTCCAC[A/T]CATGCACAAAGGTAC | 12488 |
rs51801355 | snp | C/G | | | intron-variant | Cd2ap | Mm_Celera | 17:42872148 | TTTCTGAGTTTGAGG[C/G]CAGCCTGGTCTACAA | 12488 |
rs51803796 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Cd2ap | Mm_Celera | 17:42752227 | CTTCCCCATTTTGTC[C/T]CTAAAAGTGGTTCTC | 12488 |
rs51836055 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Cd2ap | Mm_Celera | 17:42755738 | GTGACTCAGTGCTAC[A/G]CCATCCACAGCAATG | 12488 |
rs51853474 | snp | G/T | 0.142012 | 0.225474 | intron-variant, upstream-variant-2KB | Cd2ap | Mm_Celera | 17:42830931 | GTTCTTTCATTAAAT[G/T]TATACAGCAAATGCT | 12488 |
rs51862027 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Cd2ap | Mm_Celera | 17:42812564 | CAGAAACAGTGTGAG[A/C]TTGATTAGAAACTGC | 12488 |
rs51914263 | snp | C/G/T | | | intron-variant | Cd2ap | GRCm38.p3 | 17:42826697 | AAGTCCACAGGTTGT[C/G/T]GGTTATGTCAGGGAT | 12488 |
rs51921839 | snp | A/C | | | intron-variant, upstream-variant-2KB | Cd2ap | Mm_Celera | 17:42829777 | TAGAAAACAGCTTTA[A/C]TCTATGGTTCCTGTC | 12488 |
rs51925267 | snp | A/C | | | intron-variant | Cd2ap | Mm_Celera | 17:42833810 | CTGGTTCAGAAAAAA[A/C]CAAGCAAACGAACAA | 12488 |
rs51927566 | snp | C/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42835705 | TAGTTTTCAATGTTA[C/T]TAACCTTATAACTGA | 12488 |
rs51932399 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Cd2ap | Mm_Celera | 17:42842443 | TTCTCAATAAATCAG[A/G]CTGAACACAGAGTTT | 12488 |
rs51933757 | snp | A/G | | | intron-variant | Cd2ap | Mm_Celera | 17:42832379 | GAACTCAGGATCTTT[A/G]GAAGAGCAGTTGGTG | 12488 |
rs51934823 | snp | A/G | | | intron-variant, upstream-variant-2KB | Cd2ap | Mm_Celera | 17:42831063 | GAGGCAGAGGCAGGC[A/G]GATTTCTGAGTTCGA | 12488 |
rs51949255 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Cd2ap | Mm_Celera | 17:42814628 | TAGAGAAGGGTGGAT[C/T]CAAATATGACAAAGG | 12488 |
rs51949262 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Cd2ap | Mm_Celera | 17:42832063 | AGGAAAACTAGAATC[C/T]AACAGGGAAATGACA | 12488 |
rs51973816 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Cd2ap | Mm_Celera | 17:42806812 | GAAGGAAAATACCCA[A/G]TGGTTTACCAAATGG | 12488 |
rs51994733 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Cd2ap | Mm_Celera | 17:42753114 | GAGGTCTGTGTCCTT[G/T]GTCAGCTGAAGTGCT | 12488 |
rs51999361 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Cd2ap | Mm_Celera | 17:42754203 | AAAATCGAAGCTATC[C/T]CCACAAAAGGCGTGT | 12488 |
rs52001396 | snp | C/G | 0.391111 | 0.206368 | intron-variant | Cd2ap | Mm_Celera | 17:42751512 | ACAGAGATGAAATTA[C/G]AGGATGGATCTGCCT | 12488 |
rs52013189 | snp | C/G | | | intron-variant | Cd2ap | Mm_Celera | 17:42843399 | AATCCCGAACCTAAG[C/G]CTTAGGAAACAATGA | 12488 |
rs52017275 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Cd2ap | Mm_Celera | 17:42798661 | TTCCAGTTCTTTCCT[A/G]GAGACAAAGTATTAC | 12488 |
rs52119300 | snp | A/G | | | intron-variant | Cd2ap | GRCm38.p3 | 17:42805717 | TATATATATATATAT[A/G]TATATATATATATAT | 12488 |
rs52122375 | snp | A/C | 0.244898 | 0.249948 | intron-variant | Cd2ap | Mm_Celera | 17:42821091 | ATCTAGGAATACTTG[A/C]ATAAAGTAGCATTTG | 12488 |
rs52128581 | snp | A/G | | | intron-variant | Cd2ap | Mm_Celera | 17:42870502 | TCCTTTTAGGCAGGG[A/G]GGAGGGGAGGGGAGG | 12488 |
rs52133746 | snp | A/C | | | intron-variant | Cd2ap | Mm_Celera | 17:42800717 | AAAACAAACAAAAAA[A/C]CCAACAACGAAAGAG | 12488 |
rs52170358 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Cd2ap | Mm_Celera | 17:42815138 | CAGAAGAATGGACAA[A/G]CACAAGATGGCCAAA | 12488 |
rs52197580 | snp | A/C | | | intron-variant | Cd2ap | Mm_Celera | 17:42780961 | TTGTGAGTTTCAGGC[A/C]AGCCTGGGCTATGTG | 12488 |
rs52199180 | snp | A/G | | | intron-variant | Cd2ap | Mm_Celera | 17:42836197 | TAAACTAATAAAAAT[A/G]CAATGTAAAAATAAG | 12488 |
rs52207408 | snp | A/G | | | intron-variant | Cd2ap | Mm_Celera | 17:42841569 | TCTGGTGTGTCTGAA[A/G]ACAGCTACAGTGTAC | 12488 |
rs52210040 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Cd2ap | Mm_Celera | 17:42824362 | TTCATGGCAAACCAA[C/T]TGTTACTTAAATGTA | 12488 |
rs52216570 | snp | A/G | | | intron-variant | Cd2ap | Mm_Celera | 17:42800807 | GAGAAGAGAAGAGAA[A/G]AGAGAGAGAAAGAGA | 12488 |
rs52249671 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Cd2ap | Mm_Celera | 17:42815216 | ACACTATTTGGTAAA[C/G]GTGAAGCCTACTGAT | 12488 |
rs52263276 | snp | A/G | | | intron-variant | Cd2ap | Mm_Celera | 17:42810487 | AAGCACAGCATACTC[A/G]TGTAAAATGCCTTCA | 12488 |
rs52278932 | snp | A/G | | | intron-variant | Cd2ap | Mm_Celera | 17:42833820 | AAAAAACAAGCAAAC[A/G]AACAAAATTCTTCAA | 12488 |
rs52282257 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Cd2ap | Mm_Celera | 17:42815121 | CCCACTGTATAGAGA[A/G]CCAGAAGAATGGACA | 12488 |
rs52297367 | snp | C/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42865158 | GATATAGATAGATGA[C/T]TAGATGGACGGGTGG | 12488 |
rs52298984 | snp | A/G | | | intron-variant | Cd2ap | Mm_Celera | 17:42836228 | CACTATAATCAAAGC[A/G]GAGCTGAAGTGCAAT | 12488 |
rs52300428 | snp | A/G | | | intron-variant | Cd2ap | Mm_Celera | 17:42865178 | TGGACGGGTGGATGG[A/G]TGGATGGATGGATGG | 12488 |
rs52313813 | snp | C/T | | | intron-variant, upstream-variant-2KB | Cd2ap | Mm_Celera | 17:42831114 | TGAGTTCCAGGACAG[C/T]CAGGGCTATACAGAG | 12488 |
rs52321919 | snp | C/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42841586 | CAGCTACAGTGTACT[C/T]ACATATAATAATAAG | 12488 |
rs52345915 | snp | C/T | | | intron-variant, upstream-variant-2KB | Cd2ap | Mm_Celera | 17:42831123 | GGACAGCCAGGGCTA[C/T]ACAGAGAAACCCTGT | 12488 |
rs52436034 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Cd2ap | Mm_Celera | 17:42842711 | TAATGCTTTATATTT[C/T]TAAATGGCAGTCTTT | 12488 |
rs52462922 | snp | A/T | 0.297521 | 0.245442 | intron-variant | Cd2ap | Mm_Celera | 17:42802298 | TTTCTTAAAGTTTCC[A/T]AAAGAACAGTATGTG | 12488 |
rs52477305 | snp | A/G | | | intron-variant | Cd2ap | Mm_Celera | 17:42821319 | AGAAAGAAAGAAAGA[A/G]AGAGAGAGAGAGAGA | 12488 |
rs52511160 | snp | C/G | | | intron-variant | Cd2ap | Mm_Celera | 17:42789732 | ATTAGATCCAACACA[C/G]CAAAGCCAAGAAAAC | 12488 |
rs52540084 | snp | A/G | | | intron-variant | Cd2ap | Mm_Celera | 17:42846505 | TCTACATTCTAGGAT[A/G]GTCAGGACTACACAG | 12488 |
rs52550588 | snp | A/G | | | intron-variant | Cd2ap | Mm_Celera | 17:42805713 | TATATATATATATAT[A/G]TATATATATATATAT | 12488 |
rs52564270 | snp | A/C/G | | | intron-variant | Cd2ap | GRCm38.p3 | 17:42872209 | GAGAAACCCTGTCTC[A/C/G]AAAAACAAAAACAAA | 12488 |
rs52587807 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Cd2ap | Mm_Celera | 17:42836265 | AAGCTTGGAAGTACC[A/G]GAACCTTCTCCCCTA | 12488 |
rs52768399 | snp | C/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42842262 | GGTAGGTTAGGTAGG[C/T]GGGCGGGTAGCTGGG | 12488 |
rs107594910 | snp | A/T | | | intron-variant | Cd2ap | GRCm38.p3 | 17:42776797 | AAAAAAAAAACTAAA[A/T]AAAAAAAAAAAAAGA | 12488 |
rs107595322 | snp | A/G | | | intron-variant | Cd2ap | Mm_Celera | 17:42779865 | CATTGAGATGTGATG[A/G]GAGGCCTGTAAGAAG | 12488 |
rs107595834 | snp | A/C | | | intron-variant | Cd2ap | Mm_Celera | 17:42809742 | TTGTAAATTCCAGTT[A/C]CTGCCATGATCAGTG | 12488 |
rs107596121 | snp | A/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42866292 | AAATATTCTTTTTTT[A/T]AAAAAAAGATTTATT | 12488 |
rs107599870 | snp | A/G | | | intron-variant | Cd2ap | Mm_Celera | 17:42800892 | TTGAATGCTTGGTCA[A/G]TAAGAAGTAGCACTA | 12488 |
rs107600250 | snp | A/G | | | intron-variant | Cd2ap | GRCm38.p3 | 17:42782850 | GGAAAGAAAAATAAA[A/G]GAAGGAAGGAAGGAA | 12488 |
rs107601078 | snp | A/G | | | intron-variant | Cd2ap | GRCm38.p3 | 17:42791311 | CATACATACATACAT[A/G]CATACATACATACAT | 12488 |
rs107606357 | snp | A/G | | | intron-variant | Cd2ap | Mm_Celera | 17:42802810 | GGTGTTGGTGGACCT[A/G]AGAGTTCTACTTCTT | 12488 |
rs107607709 | snp | A/C/G | | | intron-variant | Cd2ap | GRCm38.p3 | 17:42827635 | AGCATTAAACCTTGA[A/C/G]ACTGAGGGGGTTTTG | 12488 |
rs107613426 | snp | C/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42841747 | ATGCACAAACATTAC[C/T]GGAATATCACAATTC | 12488 |
rs107616072 | snp | A/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42861656 | TCACAGCAACAGAAC[A/T]CTGATTAGGACAGAA | 12488 |
rs107619214 | snp | C/T | | | intron-variant | Cd2ap | GRCm38.p3 | 17:42852944 | CTTCTTACTTACTGG[C/T]TTTGTTTTTGGTTTT | 12488 |
rs107620785 | snp | A/T | | | intron-variant | Cd2ap | GRCm38.p3 | 17:42851258 | AAAAAAAAAAAAAAA[A/T]AAAGAGATGACTGAC | 12488 |
rs107626460 | snp | A/G | | | intron-variant | Cd2ap | GRCm38.p3 | 17:42833686 | TTACCCAAGTTTAAA[A/G]AAAAAAAAAAAACAA | 12488 |
rs107628509 | snp | C/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42783842 | TAACAATCTCTAGGC[C/T]GGGATCTTGGACTGC | 12488 |
rs107629285 | snp | C/T | | | utr-variant-3-prime, intron-variant | Cd2ap | Mm_Celera | 17:42795957 | ACTATAAAGCTAACC[C/T]GTCCTTCTCAAATAG | 12488 |
rs107631262 | snp | A/T | | | intron-variant | Cd2ap | GRCm38.p3 | 17:42868941 | TTTTTTTTTTTTTTT[A/T]AAGAATTATTTATTT | 12488 |
rs107632774 | snp | C/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42780445 | GGAGCATACATGCCT[C/T]GAAGAAGAGAAGGAG | 12488 |
rs107636523 | snp | C/G | | | intron-variant | Cd2ap | Mm_Celera | 17:42844822 | ATTTCTGAGTTCGAC[C/G]AGCCTGGTCTACAAA | 12488 |
rs107637184 | snp | A/T | | | intron-variant | Cd2ap | GRCm38.p3 | 17:42872416 | ATAGATATAGATATA[A/T]ATAATTTTATCTTAC | 12488 |
rs107644901 | snp | A/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42834409 | GTAAAAGAAGCACTT[A/T]AAAAAAAGAAAAACA | 12488 |
rs107646049 | snp | C/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42783334 | CAGGGTTTCTCTGTA[C/T]AGCCCTGGCTGTCCT | 12488 |
rs107647496 | snp | C/G | | | intron-variant | Cd2ap | Mm_Celera | 17:42840574 | CCAGCTAGAAATAAA[C/G]TCAACTCTGAATAAC | 12488 |
rs107650506 | snp | A/G | | | intron-variant | Cd2ap | Mm_Celera | 17:42785047 | CTAGAAATGGCGACA[A/G]AAACAATGGTGGTAT | 12488 |
rs107650517 | snp | A/G | | | intron-variant | Cd2ap | Mm_Celera | 17:42776735 | GGGAGTGGGGGTGGG[A/G]GCTTTTGGGATAGCA | 12488 |
rs107651346 | snp | A/C | | | intron-variant | Cd2ap | Mm_Celera | 17:42834967 | ACTCAGAGTTCAATT[A/C]CCAGCACCCATCATC | 12488 |
rs107651819 | snp | A/G | | | intron-variant, downstream-variant-500B | Gpr111, Cd2ap | GRCm38.p3 | 17:42748702 | CACACACACACACAC[A/G]CACACACTTGTATTT | 12488 |
rs107651978 | snp | A/G | | | intron-variant | Cd2ap | Mm_Celera | 17:42778931 | AGATGTCCCATGCTG[A/G]GATTGGGAGAGGCTG | 12488 |
rs107653941 | snp | A/G | | | intron-variant | Cd2ap | Mm_Celera | 17:42789535 | TTGCCAACCAGCAAA[A/G]CTCTCTTAAAGTTGA | 12488 |
rs107654607 | snp | C/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42811774 | TAGGAATCACAATAC[C/T]GTTTTGATATGGTTT | 12488 |
rs107656151 | snp | A/G | | | intron-variant | Cd2ap | Mm_Celera | 17:42873416 | TACTGTGCGAACAAA[A/G]CTGGCCTTGAATTCT | 12488 |
rs107656185 | snp | A/C | | | intron-variant | Cd2ap | Mm_Celera | 17:42786649 | CAACTGGCAGTAGAC[A/C]GTTCTCTTTTTCATT | 12488 |
rs107658571 | snp | A/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42859027 | TTACTTACATATAAT[A/T]AATAAATAAGTCTTA | 12488 |
rs107661239 | snp | C/G | | | intron-variant | Cd2ap | Mm_Celera | 17:42804621 | ATGTGTGTGTATGGG[C/G]GGGGGTGTCCTACTT | 12488 |
rs107661801 | snp | A/C | | | intron-variant | Cd2ap | Mm_Celera | 17:42844102 | CTCAAAAAAAAAAAC[A/C]AAAAAAAAAAAAAAA | 12488 |
rs107662484 | snp | C/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42780797 | AGGCTGAGTAGCTCA[C/T]TGGGTAGAATGTTTG | 12488 |
rs107662963 | snp | A/G | | | intron-variant | Cd2ap | Mm_Celera | 17:42801344 | AAGTGCCAGCTACTG[A/G]AAGAGAGTCCGTTTT | 12488 |
rs107664655 | snp | C/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42856832 | AGTCAACCTATATTC[C/T]GTTTTTAAAAACAAA | 12488 |
rs107665336 | snp | C/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42786686 | TTCCCAGAGATTACA[C/T]TGAAGTGATCAGGTG | 12488 |
rs107666427 | snp | A/G | | | intron-variant | Cd2ap | GRCm38.p3 | 17:42842913 | GCTGGGATTAAAGGT[A/G]TGCGCCACCACGCCC | 12488 |
rs107668237 | snp | A/C | | | intron-variant | Cd2ap | Mm_Celera | 17:42842635 | AACCCTGTCTCGAAA[A/C]AAACAAACAAACAAA | 12488 |
rs107670158 | snp | A/G | | | intron-variant | Cd2ap | Mm_Celera | 17:42856154 | TACCACACACACAAA[A/G]AGAAGAAAGAAAGAA | 12488 |
rs107672280 | snp | C/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42803053 | CCTCCTTCCCTCCAC[C/T]CCTACTCTGCTACCT | 12488 |
rs107674759 | snp | C/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42783893 | TTTTACAGCAAAATA[C/T]AATGGTGCAATGGTG | 12488 |
rs107675650 | snp | C/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42785874 | CTCTTCCAAAGGTCC[C/T]GAGTTCAAATCCCAG | 12488 |
rs107679979 | snp | A/G | | | intron-variant | Cd2ap | Mm_Celera | 17:42757249 | AAAAGCCATCAAGTC[A/G]GAGAGCCACAGAGCT | 12488 |
rs107682071 | snp | C/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42865845 | AGGCTCACCTGTGAT[C/T]CAGATCTTGAGGCTG | 12488 |
rs107684731 | snp | A/G | | | intron-variant | Cd2ap | Mm_Celera | 17:42754257 | TCTTCCCCTTTCCAT[A/G]AACAACATAGTTTCA | 12488 |
rs107684991 | snp | A/C | | | intron-variant | Cd2ap | Mm_Celera | 17:42784517 | CTACCTCTCTTCTAC[A/C]CAGCTATTGGCTGCC | 12488 |
rs107686063 | snp | A/G | | | intron-variant | Cd2ap | Mm_Celera | 17:42783729 | TCTTGCGGTTAATTT[A/G]ATGAGACCTAGATCA | 12488 |
rs107686123 | snp | A/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42805933 | TGCAAATTTTCCAAA[A/T]TTCTGACCTCAAGCA | 12488 |
rs107696070 | snp | G/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42812455 | TTAAAGCATCTCTAT[G/T]TCCATATATACATCA | 12488 |
rs107696450 | snp | A/C | | | intron-variant | Cd2ap | Mm_Celera | 17:42833652 | AAGAACTCATGAGAA[A/C]TCTTTCTTTTTTTTA | 12488 |
rs107697243 | snp | C/T | | | intron-variant | Cd2ap | GRCm38.p3 | 17:42850206 | TATCTTTTACACACA[C/T]ACACACACACATACA | 12488 |
rs107699229 | snp | A/C | | | intron-variant | Cd2ap | Mm_Celera | 17:42857217 | TACAGTAACATTACC[A/C]CTTGACATCAAATAA | 12488 |
rs107699666 | snp | A/G | | | intron-variant | Cd2ap | Mm_Celera | 17:42781735 | CTGTGAGGTTGGTAC[A/G]TAAGGAACTGTAGAA | 12488 |
rs107706724 | snp | A/G | | | intron-variant | Cd2ap | Mm_Celera | 17:42753860 | AAGTATCTCTTCTAG[A/G]GAGGCTAATTGGTCT | 12488 |
rs107707871 | snp | C/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42858355 | CAAAGTAAGCAGGAC[C/T]GGAGTGAGTGGGGCT | 12488 |
rs107708499 | snp | A/G | | | intron-variant | Cd2ap | Mm_Celera | 17:42870556 | GGGGAGGGGAGGGGA[A/G]CACCTACCCTGTATT | 12488 |
rs107709250 | snp | C/G | | | utr-variant-3-prime, intron-variant | Cd2ap | Mm_Celera | 17:42794569 | TCATTTGACTAATCA[C/G]TTAAAAATAAAATGG | 12488 |
rs107712792 | snp | A/G | | | intron-variant | Cd2ap | Mm_Celera | 17:42785970 | GAGTACTTAAATATA[A/G]TAATATAATAAATAT | 12488 |
rs107712862 | snp | C/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42807602 | AGAGAGAACCTATCT[C/T]AAAATAAAACAGGCC | 12488 |
rs107712911 | snp | A/T | | | intron-variant | Cd2ap | GRCm38.p3 | 17:42804561 | CACACACACACACAC[A/T]CACTCTCTCTCTCTC | 12488 |
rs107713128 | snp | A/C | | | intron-variant | Cd2ap | Mm_Celera | 17:42780612 | TTGTCTGGTTACTAT[A/C]GTGTCCCCTGGTTTT | 12488 |
rs107717609 | snp | G/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42791383 | TAAACTACCACTGAT[G/T]ATTTCTAACTTAAAA | 12488 |
rs107718952 | snp | A/C | | | intron-variant | Cd2ap | Mm_Celera | 17:42864311 | AAAAAAAAAAAAAAA[A/C]CTCTTATCAGATCAC | 12488 |
rs107719558 | snp | C/G | | | upstream-variant-2KB | Cd2ap | Mm_Celera | 17:42877961 | CCCAAGCAAAGAACA[C/G]AAATAAAAAATTCAT | 12488 |
rs107720133 | snp | A/G | | | intron-variant | Cd2ap | Mm_Celera | 17:42825473 | ATGTGTGAATGCATC[A/G]TGCACATGTCTGATG | 12488 |
rs107720538 | snp | C/G | | | intron-variant | Cd2ap | Mm_Celera | 17:42857775 | GCGCTATTGTCAGCT[C/G]ATGGCCTCTGGAGGA | 12488 |
rs107720712 | snp | A/T | | | upstream-variant-2KB, intron-variant | Gpr111, Cd2ap | Mm_Celera | 17:42750578 | TATAGAAATTTTTAG[A/T]CCCAATTCAGAGTTT | 12488 |
rs107723092 | snp | A/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42828187 | AAGTATCCCTCATAG[A/T]GCAAGAAGCTATAGA | 12488 |
rs107723470 | snp | A/G | | | intron-variant | Cd2ap | Mm_Celera | 17:42810803 | CCAATTATGGGGGGG[A/G]GAAATCTGATTTGTA | 12488 |
rs107724031 | snp | A/G | | | intron-variant | Cd2ap | Mm_Celera | 17:42844133 | AAAGAAAAGAAAAAA[A/G]AAAAAAAAAAAGAAA | 12488 |
rs107725659 | snp | A/G | | | intron-variant | Cd2ap | GRCm38.p3 | 17:42842917 | GGATTAAAGGTGTGC[A/G]CCACCACGCCCAGCT | 12488 |
rs107726742 | snp | A/G | | | intron-variant | Cd2ap | Mm_Celera | 17:42853346 | ACGCAGCCTTACGGA[A/G]GACCCAACCCAGAGT | 12488 |
rs107727609 | snp | C/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42844052 | GTCTACAAAGTGAGT[C/T]CCAGGACAGCCAGGG | 12488 |
rs107727872 | snp | A/G | | | utr-variant-3-prime, intron-variant | Cd2ap | Mm_Celera | 17:42794380 | TACTGTTGACTGTGT[A/G]TGTTACTTTTTACTG | 12488 |
rs107730867 | snp | C/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42804526 | AGGTAAATAGCTTTA[C/T]ACACACACACACACA | 12488 |
rs107731629 | snp | G/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42823177 | CCAACCCTGAGAAGA[G/T]AAAGGCAGTGAATGG | 12488 |
rs107731839 | snp | C/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42831409 | CCTGTACCTGACTCT[C/T]CAGCTGTACTCTCCA | 12488 |
rs107737194 | snp | G/T | | | intron-variant | Cd2ap | GRCm38.p3 | 17:42871351 | TCTCAGATAGAGAGA[G/T]AGAGAGAGAGAGAGA | 12488 |
rs107737351 | snp | A/G | | | intron-variant | Cd2ap | Mm_Celera | 17:42787160 | ATAACACAGTGGGGG[A/G]GAAACAGTTTATAGT | 12488 |
rs107737665 | snp | A/G | | | intron-variant, upstream-variant-2KB | Cd2ap | Mm_Celera | 17:42829197 | TCTGAGTTTGAGGCT[A/G]CCCTGGTCTACAGAG | 12488 |
rs107738268 | snp | A/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42782302 | ACAAGTACTGGTTTC[A/T]AGAGGCCACACCAAA | 12488 |
rs107738484 | snp | A/G | | | intron-variant, downstream-variant-500B | Cd2ap | Mm_Celera | 17:42808320 | TACGTACGTACATAC[A/G]TACATACATACATAC | 12488 |
rs107739960 | snp | G/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42815289 | ATTTTTTAAGGTTTT[G/T]GGGGGGTTTTTTGTT | 12488 |
rs107740315 | snp | A/G | | | intron-variant | Cd2ap | Mm_Celera | 17:42859064 | AAAGAATGTAGCAAT[A/G]ACAGAAAAATCTAAG | 12488 |
rs107748649 | snp | C/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42785917 | GTCTCTGTAATGGGA[C/T]CTGATGCCCTCTTCT | 12488 |
rs107748686 | snp | A/G | | | intron-variant | Cd2ap | Mm_Celera | 17:42791609 | CAGCTTCTTTAAGAA[A/G]ACAGAAAAGTATGTG | 12488 |
rs107751655 | snp | A/G | | | utr-variant-3-prime, intron-variant | Cd2ap | Mm_Celera | 17:42796229 | TCGGTAGATGTCACA[A/G]TTTATGTCCTCTTAT | 12488 |
rs107751696 | snp | G/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42792423 | GATAGCAACCTCAAT[G/T]TGTTTTCAGTCCAAC | 12488 |
rs107752683 | snp | G/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42845128 | TTCACAGCTCCTGTA[G/T]AAGGCCACCAGCTAC | 12488 |
rs107753942 | snp | A/C | | | intron-variant | Cd2ap | Mm_Celera | 17:42831347 | GCATTCTTCTAGTTT[A/C]GACAAATACACTTTC | 12488 |
rs107754013 | snp | C/G | | | intron-variant | Cd2ap | Mm_Celera | 17:42754380 | ATGGTTTCTGTCAAT[C/G]TTTTTGAATTTTTTT | 12488 |
rs107755856 | snp | A/G | | | intron-variant | Cd2ap | GRCm38.p3 | 17:42799679 | GGGGGAATGAAATAG[A/G]GGGGGGGGGGAATCA | 12488 |
rs107755944 | snp | A/G | | | intron-variant | Cd2ap | GRCm38.p3 | 17:42791315 | CATACATACATGCAT[A/G]CATACATACATAGCC | 12488 |
rs107755996 | snp | A/G | | | intron-variant | Cd2ap | Mm_Celera | 17:42754576 | ACTCCATGAAGAACT[A/G]CAATCCTGCATACAT | 12488 |
rs107756780 | snp | A/G | | | intron-variant | Cd2ap | Mm_Celera | 17:42780799 | GCTGAGTAGCTCATT[A/G]GGTAGAATGTTTGCC | 12488 |
rs107765941 | snp | A/G/T | | | intron-variant | Cd2ap | GRCm38.p3 | 17:42873654 | TTAAATCTTACAGAG[A/G/T]GTGTGTGTGTGTGTG | 12488 |
rs107766531 | snp | A/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42784559 | TCAACCAATAGTTTT[A/T]AATTAAGGCACAAGG | 12488 |
rs107768053 | snp | C/G/T | | | intron-variant | Cd2ap | GRCm38.p3 | 17:42755907 | ACACACACACACACA[C/G/T]ACACAGAGAGAAAGA | 12488 |
rs107769604 | snp | A/G | | | upstream-variant-2KB, intron-variant | Gpr111, Cd2ap | Mm_Celera | 17:42750343 | CTTTCCCCATCAGTC[A/G]TTAGTTAACAGAAAC | 12488 |
rs107770260 | snp | C/T | | | utr-variant-3-prime, intron-variant | Cd2ap | Mm_Celera | 17:42795956 | TACTATAAAGCTAAC[C/T]CGTCCTTCTCAAATA | 12488 |
rs107771746 | snp | C/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42801693 | CTCCATATTTACCTA[C/T]CACAAATTTTGTAGA | 12488 |
rs107776060 | snp | A/C | | | intron-variant | Cd2ap | Mm_Celera | 17:42789471 | ATCCTAATTGTCAGG[A/C]AAGCATGACACTCCA | 12488 |
rs107777450 | snp | C/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42781322 | CCATAGCAACACTGT[C/T]GATTATCTTGGCAAG | 12488 |
rs107777763 | snp | A/G | | | intron-variant, downstream-variant-500B | Cd2ap | Mm_Celera | 17:42808312 | TGTGTGTGTACGTAC[A/G]TACATACATACATAC | 12488 |
rs107778044 | snp | C/G | | | intron-variant | Cd2ap | Mm_Celera | 17:42786996 | CTCTCAGCCTCGCTG[C/G]TGCTGGATCACAGGT | 12488 |
rs107783553 | snp | C/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42788328 | GGCTACACAGAGAAA[C/T]CCTGTCTCAGAAAAA | 12488 |
rs107785871 | snp | A/G | | | intron-variant | Cd2ap | GRCm38.p3 | 17:42780145 | AAAATTTTATTTTAA[A/G]AGAAAGAGAGAGAGA | 12488 |
rs107786308 | snp | C/T | | | upstream-variant-2KB, intron-variant | Gpr111, Cd2ap | Mm_Celera | 17:42750117 | CCACACCACTAGGGC[C/T]AGTTCTACTATGCTG | 12488 |
rs107786645 | snp | A/G | | | intron-variant | Cd2ap | Mm_Celera | 17:42754698 | CACTCGGGAGGCAGA[A/G]GCAGGCAGATTTCTG | 12488 |
rs107791994 | snp | A/C | | | intron-variant | Cd2ap | Mm_Celera | 17:42835625 | CAAGAATACTGCTCA[A/C]TGTCACCATTTCCTT | 12488 |
rs107792702 | snp | C/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42783268 | TCTTTCTTTTTTCTT[C/T]TTTTTTTTCCTTTTT | 12488 |
rs107794690 | snp | C/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42844366 | AAGCTGGAGAGAAAG[C/T]CAACTCCACAGCCGT | 12488 |
rs107803304 | snp | A/G | | | intron-variant | Cd2ap | Mm_Celera | 17:42854241 | AGTGATTAAAGCTGA[A/G]ATACCTAAAGCTCAT | 12488 |
rs107803483 | snp | A/G | | | intron-variant | Cd2ap | Mm_Celera | 17:42780629 | TGTCCCCTGGTTTTA[A/G]TTTCCCTGCCCTGCC | 12488 |
rs107806144 | snp | A/G | | | intron-variant | Cd2ap | Mm_Celera | 17:42858234 | CGGATTTCTGAGTTC[A/G]AGGCCAGCCTGGTCT | 12488 |
rs107806545 | snp | A/G | | | intron-variant | Cd2ap | Mm_Celera | 17:42788798 | ATAAAAAGTGTACAG[A/G]CTACTGATACTGCTG | 12488 |
rs107806775 | snp | A/G | | | intron-variant | Cd2ap | Mm_Celera | 17:42780788 | GAATGTGTGAGGCTG[A/G]GTAGCTCATTGGGTA | 12488 |
rs107807751 | snp | C/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42812341 | ACTGCAATGACAGCA[C/T]TGCTACTTATAACAT | 12488 |
rs107812978 | snp | C/G | | | intron-variant | Cd2ap | Mm_Celera | 17:42854720 | TTTTTTTTTTTTTTT[C/G]GTTTTTTGAGACAGG | 12488 |
rs107813256 | snp | A/G | | | intron-variant | Cd2ap | Mm_Celera | 17:42858598 | AGTAACAAAAACAAG[A/G]GGTTAAGGAAAGTAA | 12488 |
rs107813707 | snp | A/G | | | intron-variant | Cd2ap | Mm_Celera | 17:42862251 | TAGAACTCACTTTGT[A/G]GACCAGGCTGGCCTC | 12488 |
rs107814509 | snp | A/G | | | intron-variant | Cd2ap | Mm_Celera | 17:42838605 | AAATTTGCTTTTGTG[A/G]CATAAATTTTCACTA | 12488 |
rs107815325 | snp | A/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42855493 | AAATCTCTAAATTCT[A/T]CTTACATAACTACTC | 12488 |
rs107816154 | snp | C/G/T | | | synonymous-codon, nc-transcript-variant | Cd2ap | GRCm38.p3 | 17:42816537 | AGTGGGCTTTTTGGG[C/G/T]GGGACTTGAGGAGCA | 12488 |
rs107816319 | snp | G/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42778589 | CAGCTCACTCAACCT[G/T]GCCAGTTCTTCTGTC | 12488 |
rs107816840 | snp | C/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42837529 | ATTTGAGATCTGACA[C/T]GCTGCCATACTTGAA | 12488 |
rs107817360 | snp | A/G | | | intron-variant | Cd2ap | Mm_Celera | 17:42867161 | AAAAAGAAAAAAAAA[A/G]AAAAAAAAAAGAAAG | 12488 |
rs107820374 | snp | G/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42859287 | CTCGCTCTAAATGAA[G/T]ATAATATAGAAAAAG | 12488 |
rs107822472 | snp | C/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42835039 | CAGCACACACATGCA[C/T]ACAGACTCGCACACA | 12488 |
rs107823739 | snp | A/T | | | intron-variant, downstream-variant-500B | Cd2ap | GRCm38.p3 | 17:42808609 | TGCATTTTCTTAAAT[A/T]AAAAAAAAAATCATA | 12488 |
rs107824686 | snp | A/G | | | intron-variant | Cd2ap | Mm_Celera | 17:42802272 | CATGTATAGTGTTTT[A/G]CCTTCTAATGTTTCT | 12488 |
rs107835315 | snp | A/C | | | intron-variant, upstream-variant-2KB | Cd2ap | Mm_Celera | 17:42831036 | GCGCACGCCTTTAAT[A/C]CCAGCACTCGGGAGG | 12488 |
rs107837121 | snp | G/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42779180 | TTATCTTCCCAAGAT[G/T]GAATAAATCCTCTGC | 12488 |
rs107837997 | snp | A/G | | | intron-variant | Cd2ap | Mm_Celera | 17:42827596 | CTCTCAACCTACAAA[A/G]CCGCAACCGCATGCA | 12488 |
rs107841721 | snp | A/T | | | intron-variant | Cd2ap | GRCm38.p3 | 17:42805751 | TATATATATATATAT[A/T]AAGCATTCCTCATCT | 12488 |
rs107842147 | snp | A/G | | | intron-variant | Cd2ap | Mm_Celera | 17:42800489 | CTTACTATTATAACC[A/G]TAAATTAATGTATCT | 12488 |
rs107844192 | snp | A/G | | | intron-variant | Cd2ap | Mm_Celera | 17:42784792 | TATTTTTCTGCCCAC[A/G]GGTAAGAGTAGCTAC | 12488 |
rs107846809 | snp | A/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42818562 | TTCTTTAAAAAAAAA[A/T]TCCAGAAAAAAGAAA | 12488 |
rs107847117 | snp | A/G | | | intron-variant | Cd2ap | Mm_Celera | 17:42867222 | AAAGAAAAAGAAAAA[A/G]AAGCATTTTATTTTG | 12488 |
rs107848421 | snp | C/T | | | intron-variant | Cd2ap | GRCm38.p3 | 17:42842912 | TGCTGGGATTAAAGG[C/T]GTGCGCCACCACGCC | 12488 |
rs107848860 | snp | G/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42779349 | TCACTCTTTTTTCTA[G/T]CTGGGATGGAGATAT | 12488 |
rs107849137 | snp | C/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42843861 | GCCAGAAAGCGGGAG[C/T]GGGTAGGTGGGGAGC | 12488 |
rs107851618 | snp | G/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42782640 | GGAACCCTTTCCTCC[G/T]ACTAGGTTACCTGGT | 12488 |
rs107851756 | snp | G/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42842064 | ATCAACAATCTCAGG[G/T]AAGGATGGTAAAACA | 12488 |
rs107853222 | snp | A/G | | | intron-variant | Cd2ap | Mm_Celera | 17:42867186 | AGAAAGAAAAGAAAA[A/G]AAAAAAAGAAAAAGA | 12488 |
rs107854650 | snp | A/G | | | intron-variant | Cd2ap | Mm_Celera | 17:42790333 | GATTGGGGCTAAGAG[A/G]AAAGGAATATTGGAA | 12488 |
rs107856488 | snp | A/C | | | intron-variant | Cd2ap | Mm_Celera | 17:42864283 | GTTAAAAAAAAAAAA[A/C]AAAAACAAAACAAAA | 12488 |
rs107858649 | snp | C/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42802540 | AGGTAACATGCAAAA[C/T]ACACACACACACACA | 12488 |
rs107860589 | snp | C/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42787496 | CTCAAGCTGGATATA[C/T]GGACAGCCTCAGACC | 12488 |
rs107864874 | snp | C/G | | | intron-variant | Cd2ap | GRCm38.p3 | 17:42810403 | GTAGAAAAAAAAAAA[C/G]AGAAAAATGTGGAAG | 12488 |
rs107865162 | snp | C/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42778402 | CTGAGATGTTAGTGA[C/T]GCTCCATTTGCATGG | 12488 |
rs107868027 | snp | G/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42862171 | CATGAAAATTTCTGG[G/T]TTTGTTTGTTTGTTT | 12488 |
rs107871251 | snp | A/G | | | intron-variant | Cd2ap | Mm_Celera | 17:42787604 | CTAAAAGCATTGGCT[A/G]CTCTTGCAGAGACCC | 12488 |
rs107871665 | snp | A/G | | | intron-variant | Cd2ap | Mm_Celera | 17:42857556 | GAACACAACATGGAA[A/G]TTTGACATTTCTAAA | 12488 |
rs107873111 | snp | A/G | | | intron-variant | Cd2ap | GRCm38.p3 | 17:42876202 | AGAGGGCGCAGGGCA[A/G]CGGGTCACGGGTTCG | 12488 |
rs107873682 | snp | A/G | | | intron-variant | Cd2ap | Mm_Celera | 17:42780157 | TAAAAGAAAGAGAGA[A/G]AGATTGTCTGCAGCA | 12488 |
rs107875563 | snp | A/C | | | intron-variant | Cd2ap | Mm_Celera | 17:42784987 | AAGACTGTAAGAGTC[A/C]GAACACTAGGACGTC | 12488 |
rs107878101 | snp | A/G | | | intron-variant | Cd2ap | Mm_Celera | 17:42822547 | TATATTATTACATCC[A/G]AACAGATTCCTTGAT | 12488 |
rs107879766 | snp | A/C | | | intron-variant | Cd2ap | Mm_Celera | 17:42865449 | CAAGGTTTGAATATG[A/C]TTAGCCTAGGAAGTG | 12488 |
rs107879875 | snp | A/G | | | intron-variant | Cd2ap | Mm_Celera | 17:42800072 | AAACCTTACAGGCTA[A/G]TACAGATGCTAATCA | 12488 |
rs107879931 | snp | A/G | | | intron-variant | Cd2ap | Mm_Celera | 17:42852092 | GATGGGGGAAGGAGG[A/G]AATGAGAGAAGAGCA | 12488 |
rs107880149 | snp | C/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42798880 | TTCTTCCAGAGGACC[C/T]GAGTTCGCGGTCTGT | 12488 |
rs107880210 | snp | C/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42813323 | AATATATATCAAAGT[C/T]ACACATGTAGACATT | 12488 |
rs107883775 | snp | A/G | | | intron-variant | Cd2ap | Mm_Celera | 17:42856719 | TCAAATTTAGATGGA[A/G]TAGGAATGTTCAATC | 12488 |
rs107884228 | snp | G/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42803765 | TCAACATTTAAAGAG[G/T]AAAAAATATACAGCT | 12488 |
rs107884565 | snp | A/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42786581 | TAACTTCAGCTTGGG[A/T]CAAATTGACACATAA | 12488 |
rs107885551 | snp | A/C | | | intron-variant | Cd2ap | GRCm38.p3 | 17:42872237 | AAAAACAAAACAAAA[A/C]AAAAAAAAAAAAAAG | 12488 |
rs107888048 | snp | A/G | | | intron-variant | Cd2ap | GRCm38.p3 | 17:42846222 | GGGTGGGGGGGGGGG[A/G]GAAATGTTCACAAAT | 12488 |
rs107888895 | snp | A/C | | | intron-variant | Cd2ap | Mm_Celera | 17:42859417 | TAAGGCATGGCTCCA[A/C]TGAAAGACTAGATTT | 12488 |
rs107889461 | snp | A/G | | | intron-variant | Cd2ap | Mm_Celera | 17:42862237 | AGCCCTGGCTGTCCT[A/G]GAACTCACTTTGTAG | 12488 |
rs107889677 | snp | A/G | | | intron-variant | Cd2ap | Mm_Celera | 17:42861059 | TGTAACCTATGTTGG[A/G]CTTCAAATTCACAGA | 12488 |
rs107890229 | snp | A/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42861070 | TTGGACTTCAAATTC[A/T]CAGAAATCTTGCCTC | 12488 |
rs107892674 | snp | A/G | | | intron-variant | Cd2ap | Mm_Celera | 17:42754476 | CAGCTTTTGCACAGG[A/G]TCAGAGTTCATTTCC | 12488 |
rs107893085 | snp | C/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42785403 | CTTGGAGATGTGTCA[C/T]GAGGGGTAGACTCCG | 12488 |
rs107894812 | snp | C/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42863951 | ACAAGCATTTTGTCC[C/T]CACTGTCCTATATAG | 12488 |
rs107897532 | snp | A/G | | | intron-variant | Cd2ap | Mm_Celera | 17:42825105 | ATCCTAATTTAAGCA[A/G]TCATTTATTTCTTTA | 12488 |
rs107898416 | snp | C/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42832112 | ATGCCTATTACCTTA[C/T]TTCCTGTTCATGCCT | 12488 |
rs107899040 | snp | G/T | | | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | Cd2ap | GRCm38.p3 | 17:42876473 | GGGTGGGAGGGGGGG[G/T]GGAGAACGGGGTCCG | 12488 |
rs107899226 | snp | A/G | | | intron-variant | Cd2ap | Mm_Celera | 17:42864137 | TGAGCACTTCTGTTT[A/G]CAATAATATACATAA | 12488 |
rs107900014 | snp | A/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42820143 | TATATATATATATAT[A/T]TTAAATTCTTACTTT | 12488 |
rs107900111 | snp | A/G | | | intron-variant | Cd2ap | Mm_Celera | 17:42817532 | CAGCTTGTGAAAAAC[A/G]GCAATCTGATCATCC | 12488 |
rs107902056 | snp | A/C | | | intron-variant | Cd2ap | Mm_Celera | 17:42867758 | GCCATACCTTGTGGG[A/C]AGGGCCTAAGGGATG | 12488 |
rs107902583 | snp | A/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42849932 | GTAAAACCCATCTTT[A/T]AAAAAAAAAAAAAAA | 12488 |
rs107910320 | snp | C/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42754565 | ACCCTCTTTTGACTC[C/T]ATGAAGAACTGCAAT | 12488 |
rs107910854 | snp | A/G | | | intron-variant | Cd2ap | Mm_Celera | 17:42803825 | TCAAAGTACCCAAAA[A/G]AGACCTGGCATATCA | 12488 |
rs107911259 | snp | A/G | | | intron-variant | Cd2ap | Mm_Celera | 17:42858416 | ATTCCTAACAGCCAC[A/G]TGATGGCTCACAATC | 12488 |
rs107911275 | snp | A/G | | | intron-variant | Cd2ap | Mm_Celera | 17:42839933 | AAATTGTGTCTGGAT[A/G]TGTTCTTCTTTCTCC | 12488 |
rs107911603 | snp | A/G | | | intron-variant | Cd2ap | Mm_Celera | 17:42854040 | CATTTCAATCAAAAA[A/G]AAATTAAGGTAAAAA | 12488 |
rs107914268 | snp | A/C | | | intron-variant | Cd2ap | Mm_Celera | 17:42788554 | GATCGTTTTAAAAAA[A/C]CAACCAAAAACCCTA | 12488 |
rs107915850 | snp | C/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42837797 | CTAATTTTAGGTTAG[C/T]TTCTTATGTATCAAG | 12488 |
rs107919183 | snp | C/T | | | intron-variant | Cd2ap | GRCm38.p3 | 17:42876053 | GTGTGTGTGTGTGCG[C/T]GTGCATAGTAGATGT | 12488 |
rs107919370 | snp | A/C/G | | | intron-variant | Cd2ap | GRCm38.p3 | 17:42753479 | CCCTCTTCCCCCTTC[A/C/G]CCCCTCTCCCCTTCT | 12488 |
rs107919747 | snp | C/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42802404 | GAAAGATGGCTCAAA[C/T]GCTAAAAGCACTAGC | 12488 |
rs107920249 | snp | A/G | | | intron-variant | Cd2ap | Mm_Celera | 17:42803970 | ATATGTGTGTATAAT[A/G]TATGTATACATACAC | 12488 |
rs107923098 | snp | G/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42862175 | AAAATTTCTGGTTTT[G/T]TTTGTTTGTTTGTTT | 12488 |
rs107924113 | snp | A/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42801576 | AATTAAAATATTTTT[A/T]AAAAATCACCATAAG | 12488 |
rs107924460 | snp | C/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42755361 | CGAGTTCCACAGCTC[C/T]ACCTCTCTTCTCTTC | 12488 |
rs107924513 | snp | C/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42797127 | TGTGAGGACAGGCTT[C/T]GTCTTACTCCTGGGC | 12488 |
rs107926043 | snp | C/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42783393 | TTGAACTCAGAACTC[C/T]GCCTGCCTCTGCCTC | 12488 |
rs107926896 | snp | A/G | | | intron-variant | Cd2ap | Mm_Celera | 17:42781891 | AGCCCAGGCGGAGTC[A/G]AAGGTACACCGTCTA | 12488 |
rs107927964 | snp | C/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42861088 | GAAATCTTGCCTCAA[C/T]CTCTCCAGTACTGGG | 12488 |
rs107928720 | snp | A/C | | | intron-variant | Cd2ap | Mm_Celera | 17:42807558 | AAGTCTGGTCAACAT[A/C]AGACGGTACAGAGCA | 12488 |
rs107935070 | snp | G/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42872966 | ATGTCTCTAGTAGTA[G/T]TAATCCTTAAGTTTT | 12488 |
rs107939153 | snp | C/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42813215 | TGAGTGGCAACATGA[C/T]TACCAGTGGATAATT | 12488 |
rs107939162 | snp | G/T | | | intron-variant | Cd2ap | GRCm38.p3 | 17:42776921 | ATGTGTATATATATA[G/T]AGAGAGAGTCTTACA | 12488 |
rs107941171 | snp | A/G | | | intron-variant | Cd2ap | Mm_Celera | 17:42790004 | TGGGATAGGTATTCT[A/G]ATGGATGGTTATGTA | 12488 |
rs107941222 | snp | A/G | | | intron-variant | Cd2ap | Mm_Celera | 17:42799188 | AGCAGGAGGGGGGGG[A/G]AGGAGGAGGAGGAGG | 12488 |
rs107943890 | snp | A/G | | | intron-variant | Cd2ap | Mm_Celera | 17:42863039 | AAAATAAAGCTCTCT[A/G]CACTCCTTGAGCTTA | 12488 |
rs107944376 | snp | A/C | | | intron-variant | Cd2ap | Mm_Celera | 17:42847533 | TGCTTACCCTCACCC[A/C]TTGGAAGAGCTAGCT | 12488 |
rs107944456 | snp | A/G | | | intron-variant | Cd2ap | GRCm38.p3 | 17:42805649 | CAATTAATGCTGTGT[A/G]TGTGTGTGTGTGTGT | 12488 |
rs107945381 | snp | A/G | | | intron-variant | Cd2ap | GRCm38.p3 | 17:42864991 | GGGAGGCGAGGCGTA[A/G]TAACACCCAGCTTGA | 12488 |
rs107947530 | snp | A/G | | | intron-variant | Cd2ap | Mm_Celera | 17:42837367 | ATACAGCTGTACTTG[A/G]GAGTTGTGAAACTGC | 12488 |
rs107947774 | snp | C/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42755012 | GTTTTGCCCCCAATC[C/T]TGATCCCATGTTCAG | 12488 |
rs107950792 | snp | A/G | | | intron-variant | Cd2ap | Mm_Celera | 17:42783535 | ATAAGAGGTATTGAT[A/G]AATGCTTTTGTAGAA | 12488 |
rs107954684 | snp | A/G | | | intron-variant | Cd2ap | Mm_Celera | 17:42853809 | TTAATCCCAGCACTC[A/G]AAAGGCAGAGGCAGG | 12488 |
rs107956086 | snp | A/G | | | intron-variant | Cd2ap | Mm_Celera | 17:42754690 | AATCCCAGCACTCGG[A/G]AGGCAGAGGCAGGCA | 12488 |
rs107957048 | snp | A/G | | | intron-variant | Cd2ap | Mm_Celera | 17:42853922 | AAAAGAGGAAAAAAA[A/G]AAAAAAAAAACAGAT | 12488 |
rs107957490 | snp | A/G | | | intron-variant | Cd2ap | Mm_Celera | 17:42779476 | ATGTTACACAAAGAC[A/G]ATCTCCTAACATAAC | 12488 |
rs107957704 | snp | C/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42754654 | AAAAATTGAGCCGGG[C/T]GTAGTGGCACACACG | 12488 |
rs107960867 | snp | C/G | | | intron-variant | Cd2ap | Mm_Celera | 17:42823406 | GGATAATGACTCGAG[C/G]AGAATGTAAAAGCGA | 12488 |
rs107965966 | snp | G/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42757141 | TGGAGTTACAATAGC[G/T]CTTAAATGTCAGTTT | 12488 |
rs107967043 | snp | A/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42813364 | TGATATGATATGATA[A/T]GAGAGCCTATCTGCT | 12488 |
rs107967546 | snp | G/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42837246 | GGTCCCATCAAGAAC[G/T]GATCATTTCTGTGCT | 12488 |
rs107967903 | snp | A/G | | | intron-variant | Cd2ap | Mm_Celera | 17:42814116 | ACATACAGACATGTA[A/G]GGGGGGGGGGGCTTT | 12488 |
rs107968391 | snp | A/C | | | intron-variant | Cd2ap | GRCm38.p3 | 17:42844101 | CCTCAAAAAAAAAAA[A/C]CAAAAAAAAAAAAAA | 12488 |
rs107973431 | snp | C/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42801015 | CTGCAGATCAAGATG[C/T]AGAACCTTAGCCCCT | 12488 |
rs107980062 | snp | A/C | | | intron-variant | Cd2ap | Mm_Celera | 17:42867497 | TTTAAATCAAAAAAA[A/C]CTTTCAATCAACTGT | 12488 |
rs107981922 | snp | G/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42797335 | CACCATTCTAAACTC[G/T]GTTTCACCTTTGTAG | 12488 |
rs107983121 | snp | A/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42806792 | GGATTTATTTTTTTT[A/T]TAAGGAAGGAAAATA | 12488 |
rs107984644 | snp | A/G | | | intron-variant | Cd2ap | Mm_Celera | 17:42862046 | GAGCCTAACTCCCCC[A/G]CATCCTGGGATAAGC | 12488 |
rs107985557 | snp | A/G | | | intron-variant | Cd2ap | Mm_Celera | 17:42862540 | CACCATGTGGTTGCT[A/G]GAATTTGAACTCAGG | 12488 |
rs107986941 | snp | G/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42788660 | TCAAAATCCACTCAA[G/T]GAAATTATAGAAAAA | 12488 |
rs107987998 | snp | A/C | | | intron-variant | Cd2ap | Mm_Celera | 17:42843700 | TGTCTAGTACCAAAC[A/C]ATGAAAACATACATA | 12488 |
rs107988051 | snp | C/G | | | intron-variant | Cd2ap | GRCm38.p3 | 17:42875474 | ACACCAAGCTGGGGG[C/G]GGGGGGGCGGGGGAG | 12488 |
rs107990597 | snp | A/C/T | | | intron-variant | Cd2ap | GRCm38.p3 | 17:42857265 | AGTTCCACACTGGAC[A/C/T]ATTTACAGCCCAAGG | 12488 |
rs107991603 | snp | C/G | | | intron-variant | Cd2ap | Mm_Celera | 17:42824634 | TGTGTGTGTGTGTGT[C/G]AAATTTACCATAATC | 12488 |
rs107994611 | snp | C/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42784830 | CCTCCAAGAAGCTTC[C/T]TTTTAGCAAATAGCA | 12488 |
rs107995656 | snp | C/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42801916 | CCTACATTTTTTCAG[C/T]CATTCTGTATCTATA | 12488 |
rs107995883 | snp | A/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42856843 | ATTCTGTTTTTAAAA[A/T]CAAAGTATCAAAGAC | 12488 |
rs108000716 | snp | C/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42757408 | GGAGGGCAGGCTGCA[C/T]GGGTGAGGGTGTGGA | 12488 |
rs108003273 | snp | A/C | | | intron-variant | Cd2ap | Mm_Celera | 17:42755346 | CTCCCTCCACTCCTA[A/C]GAGTTCCACAGCTCT | 12488 |
rs108004348 | snp | A/G | | | intron-variant | Cd2ap | Mm_Celera | 17:42754496 | AGTTCATTTCCTAAC[A/G]CCTATGGCAGGTCGT | 12488 |
rs108005271 | snp | C/G | | | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | Cd2ap | GRCm38.p3 | 17:42876572 | GGCGGGGTCTCGCAC[C/G]GTCAGCCCGCACCCG | 12488 |
rs108005298 | snp | A/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42806793 | GATTTATTTTTTTTT[A/T]AAGGAAGGAAAATAC | 12488 |
rs108006466 | snp | A/G | | | intron-variant | Cd2ap | Mm_Celera | 17:42861304 | ACTATATTGGTTTGA[A/G]TAAGAATGGTCCCCA | 12488 |
rs108016099 | snp | A/G | | | upstream-variant-2KB, intron-variant | Gpr111, Cd2ap | Mm_Celera | 17:42750250 | TCCAAGTGGGGAGGG[A/G]TGAAGACTATGGAGG | 12488 |
rs108016667 | snp | A/C | | | intron-variant | Cd2ap | Mm_Celera | 17:42854096 | ACGTCACTTCCATTC[A/C]ATTTTGCTCAGAAAG | 12488 |
rs108019873 | snp | A/G | | | intron-variant | Cd2ap | GRCm38.p3 | 17:42755919 | ACATACACAGAGAGA[A/G]AGAGAGAGAGAGAGA | 12488 |
rs108020757 | snp | A/G | | | intron-variant | Cd2ap | Mm_Celera | 17:42834644 | TGAAATAGCACTCAC[A/G]CATTACTGGGCCTTG | 12488 |
rs108021189 | snp | A/T | | | upstream-variant-2KB | Cd2ap | GRCm38.p3 | 17:42876938 | CTTTCTTTTTTATTT[A/T]TTTTTTTTTTTTGCA | 12488 |
rs108025658 | snp | A/C | | | intron-variant | Cd2ap | Mm_Celera | 17:42778160 | GCAGCATCATCAGAA[A/C]CAGCAGAGGTGACAG | 12488 |
rs108026291 | snp | G/T | | | upstream-variant-2KB, intron-variant | Gpr111, Cd2ap | Mm_Celera | 17:42750370 | AAACCTTACATGCTT[G/T]CCTGCAGCTGGATCT | 12488 |
rs108026760 | snp | C/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42843540 | CACCTAAACATGAGG[C/T]ATACAAAGATGACAC | 12488 |
rs108029552 | snp | C/G | | | intron-variant | Cd2ap | Mm_Celera | 17:42870221 | TCTCCAAGGGGGGGG[C/G]GGGGCAGAAAGCAAG | 12488 |
rs108031183 | snp | G/T | | | intron-variant | Cd2ap | GRCm38.p3 | 17:42846210 | AAAGAAGTTGGGGGG[G/T]GGGGGGGGGGGAGAA | 12488 |
rs108031818 | snp | C/G | | | intron-variant | Cd2ap | Mm_Celera | 17:42822941 | CCCCAACAAAGGCTT[C/G]GGAACACTGTAGAAG | 12488 |
rs108034754 | snp | A/G | | | intron-variant | Cd2ap | GRCm38.p3 | 17:42859052 | GTCTTAAAAAAAAAA[A/G]AATGTAGCAATGACA | 12488 |
rs108036417 | snp | A/G | | | intron-variant | Cd2ap | Mm_Celera | 17:42853500 | CTGGGCAGGAGGGAT[A/G]GTGATTGTGAGCTAC | 12488 |
rs108044134 | snp | C/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42860909 | AACACACAAAACCTA[C/T]ACTAGGAGAAGTAAC | 12488 |
rs108048006 | snp | C/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42781646 | GTGGATTCCTGTAGG[C/T]TCCCAGGGGAAGACA | 12488 |
rs108053559 | snp | A/G | | | intron-variant | Cd2ap | Mm_Celera | 17:42789394 | TAAAAGCTGTATGGG[A/G]AAACCGTCAACTCCC | 12488 |
rs108053607 | snp | A/G | | | intron-variant | Cd2ap | Mm_Celera | 17:42859462 | AGAATGCTATCCTCC[A/G]TTACTTTGATAACAG | 12488 |
rs108054223 | snp | C/G | | | intron-variant | Cd2ap | Mm_Celera | 17:42801337 | TATTGGCAAGTGCCA[C/G]CTACTGAAAGAGAGT | 12488 |
rs108057682 | snp | A/G | | | utr-variant-3-prime, intron-variant | Cd2ap | Mm_Celera | 17:42796298 | TCAGTTAAGTTCATG[A/G]ATCATTAGGAACACT | 12488 |
rs108057920 | snp | A/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42828282 | ACATTTTTTTTTTTT[A/T]AAGAAAGCATTTCAC | 12488 |
rs108059948 | snp | A/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42784077 | AAATCTCTCAGTTTC[A/T]ATTCCAAGCACCTAC | 12488 |
rs108062048 | snp | A/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42783192 | AGTTCCATTTATTAT[A/T]AGCTGTGTGGGCTTG | 12488 |
rs108063774 | snp | G/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42776919 | ATATGTGTATATATA[G/T]AGAGAGAGAGTCTTA | 12488 |
rs108067205 | snp | A/G | | | intron-variant | Cd2ap | Mm_Celera | 17:42861957 | TGTTTGCTTAACTCA[A/G]CATTTTCTCCCTTTC | 12488 |
rs108067366 | snp | C/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42755994 | GCTTGGTCCACTAAA[C/T]CTACTGTAAATAGTA | 12488 |
rs108070041 | snp | A/G | | | upstream-variant-2KB | Cd2ap | GRCm38.p3 | 17:42877111 | GTTTTTCTTTGGGGT[A/G]GGTGAGAAACGCAGT | 12488 |
rs108070823 | snp | C/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42845701 | CACAGTGAAATAAAC[C/T]ATGACATAGCTCATT | 12488 |
rs108070866 | snp | C/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42859575 | CTTTAGGAATCTGAA[C/T]CCTTTGGAACTACAG | 12488 |
rs108078802 | snp | A/G | | | intron-variant | Cd2ap | GRCm38.p3 | 17:42800809 | GAAGAGAAGAGAAAA[A/G]AGAGAGAAAGAGAAA | 12488 |
rs108079143 | snp | A/G | | | intron-variant | Cd2ap | GRCm38.p3 | 17:42823144 | CCACCCCCACTTCTC[A/G]CCCCCCCCCACCCCT | 12488 |
rs108079645 | snp | C/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42802938 | TTCAATAAGGCCACA[C/T]TTCCTAATAGTGCCA | 12488 |
rs108080952 | snp | A/G | | | intron-variant | Cd2ap | Mm_Celera | 17:42778857 | CTTAAGTATAGGTAC[A/G]TGTTCCTTGTTCTGC | 12488 |
rs108083061 | snp | A/C | | | intron-variant | Cd2ap | Mm_Celera | 17:42861099 | TCAACCTCTCCAGTA[A/C]TGGGATTTAGGATTA | 12488 |
rs108085372 | snp | A/G | | | intron-variant | Cd2ap | Mm_Celera | 17:42861261 | AGAACTGAGAAAAAA[A/G]ATGAAAACCTAATGA | 12488 |
rs108085836 | snp | A/G | | | intron-variant, utr-variant-5-prime | Cd2ap | Mm_Celera | 17:42828944 | CTCCAAAATACAGAC[A/G]CTGGGGACAGAGACC | 12488 |
rs108088236 | snp | A/G | | | intron-variant | Cd2ap | Mm_Celera | 17:42861745 | TGGACAATGACTTAT[A/G]ATATCAATGCACAAC | 12488 |
rs108091171 | snp | C/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42790567 | ATACTTCCCTCACCC[C/T]CAATTAAAATTAGTT | 12488 |
rs108091793 | snp | C/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42755300 | CTTTTTCATTCTTCC[C/T]TCCTACAATGCATTC | 12488 |
rs108091823 | snp | A/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42818173 | TCCAAGTGCTCTCTC[A/T]GTGTAGAGCCCTCAC | 12488 |
rs108091828 | snp | A/C | | | intron-variant | Cd2ap | Mm_Celera | 17:42782975 | AAATCATCCTGATTA[A/C]ATTATGTAAGTTCTC | 12488 |
rs108094655 | snp | C/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42825514 | TCAAAAGAGGGTATC[C/T]GATCCCCTGGAACTA | 12488 |
rs108094929 | snp | A/C | | | intron-variant | Cd2ap | Mm_Celera | 17:42853469 | GTGCAGATGCCTGTG[A/C]AATCTGACAGATCCT | 12488 |
rs108096341 | snp | A/G | | | intron-variant | Cd2ap | Mm_Celera | 17:42835584 | TGCTATGGATGCTAA[A/G]GGGTTTTAGTAACAG | 12488 |
rs108100162 | snp | A/G | | | intron-variant | Cd2ap | Mm_Celera | 17:42797501 | CAAAACCCCATAGAA[A/G]AAGGGTGATGATACT | 12488 |
rs108103628 | snp | A/G | | | intron-variant | Cd2ap | Mm_Celera | 17:42784786 | AAATCTTATTTTTCT[A/G]CCCACGGGTAAGAGT | 12488 |
rs108110134 | snp | C/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42868144 | TAAATTTGCTTTTCC[C/T]GTTAGTAAGAGGATA | 12488 |
rs108113754 | snp | A/G | | | intron-variant | Cd2ap | Mm_Celera | 17:42864709 | TCACACACAGAATAC[A/G]CAAACAAAAGACATT | 12488 |
rs108115046 | snp | C/G | | | intron-variant | Cd2ap | Mm_Celera | 17:42844081 | GGTTATACAGAAAAA[C/G]CCTGCCTCAAAAAAA | 12488 |
rs108116165 | snp | C/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42853287 | CAAATAATCCATCCA[C/T]GGAAGAACCCCTTGT | 12488 |
rs108119219 | snp | C/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42785417 | ACGAGGGGTAGACTC[C/T]GAGGCTTCAAAAACC | 12488 |
rs108120219 | snp | A/T | | | upstream-variant-2KB | Cd2ap | GRCm38.p3 | 17:42877303 | GCCGGCGTAGGATTA[A/T]TGTAATCAAACACGA | 12488 |
rs108123980 | snp | A/G | | | intron-variant | Cd2ap | Mm_Celera | 17:42864988 | CTTGGGAGGCGAGGC[A/G]TAATAACACCCAGCT | 12488 |
rs108126947 | snp | C/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42837283 | TTTCACTCTTGATAG[C/T]TTTCTAAGTGGTTCT | 12488 |
rs108128794 | snp | A/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42851053 | AGCTAAAGAGATGAC[A/T]GACGGGCTGGCGAGA | 12488 |
rs108129745 | snp | C/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42802030 | TTTTCTTATTTTTCT[C/T]TCTTTTTCTATTATT | 12488 |
rs108131545 | snp | A/C | | | intron-variant | Cd2ap | Mm_Celera | 17:42804688 | GTTGAGTGCATTAAC[A/C]TCACACTCTGGGCTT | 12488 |
rs108132531 | snp | G/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42806583 | GTGTGGGTGTGGGTG[G/T]GTGGGTGTGTAGAGT | 12488 |
rs108132732 | snp | A/C | | | intron-variant | Cd2ap | Mm_Celera | 17:42755870 | AAGCCATTGAGAAAG[A/C]CTTCAACCTCAATCT | 12488 |
rs108138533 | snp | C/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42812565 | AGAAACAGTGTGAGC[C/T]TGATTAGAAACTGCC | 12488 |
rs108140717 | snp | A/G | | | intron-variant | Cd2ap | Mm_Celera | 17:42853307 | GAACCCCTTGTGAAA[A/G]CCCAACCCTGATGAA | 12488 |
rs108142940 | snp | C/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42754594 | ATCCTGCATACATAC[C/T]CCACATAGACACACA | 12488 |
rs108143764 | snp | C/T | | | upstream-variant-2KB, intron-variant | Gpr111, Cd2ap | Mm_Celera | 17:42750236 | GCATTCCCAACCACT[C/T]CAAGTGGGGAGGGGT | 12488 |
rs108143797 | snp | A/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42786329 | TTCGTCACCAAAGGA[A/T]GTCAGGACTGGAACT | 12488 |
rs108145675 | snp | A/G | | | intron-variant | Cd2ap | Mm_Celera | 17:42868534 | TGTACCACCACGTCC[A/G]GCTCAAAGAATTGTT | 12488 |
rs108146679 | snp | G/T | | | intron-variant | Cd2ap | Mm_Celera | 17:42828465 | CTCAAAGATCAGAAA[G/T]GACAGGAAGCAGAAG | 12488 |