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 |