SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs3663930 | snp | C/T | 0.48 | 0.0979796 | intron-variant | 4930595M18Rik | GRCm38.p3 | X:81453176 | TTTGGAAAAATAATC[C/T]TTATATACAATACCA | 245492 |
rs29121534 | snp | C/T | 0.277778 | 0.248452 | intron-variant | 4930595M18Rik | Mm_Celera | X:81449558 | GTAGAGAAATGCCAC[C/T]GATTTGTACCAATAG | 245492 |
rs29121537 | snp | C/T | 0.32 | 0.24 | intron-variant | 4930595M18Rik | Mm_Celera | X:81449147 | GCTCTGTAGTACAGC[C/T]TGAATTCTGGGATGA | 245492 |
rs29121539 | snp | A/G | 0.444444 | 0.157135 | intron-variant | 4930595M18Rik | Mm_Celera | X:81445140 | GACAGATTCCAATCT[A/G]CCTCTGGGTGGTGCA | 245492 |
rs29121540 | snp | A/T | 0.231111 | 0.249285 | intron-variant | 4930595M18Rik | Mm_Celera | X:81445029 | GGTTTCATATGCATC[A/T]CTTTCTATTACAAAA | 245492 |
rs29121541 | snp | A/G | 0.231111 | 0.249285 | intron-variant | 4930595M18Rik | Mm_Celera | X:81430295 | TGGAGTTAGAGCACG[A/G]TTTCTAAACATAATA | 245492 |
rs29121542 | snp | C/T | 0.465374 | 0.126941 | intron-variant | 4930595M18Rik | Mm_Celera | X:81430181 | ACTAGTAGACTCTTC[C/T]TTGTATGCATGAAAG | 245492 |
rs29121543 | snp | C/T | 0.132653 | 0.220748 | intron-variant | 4930595M18Rik | Mm_Celera | X:81430077 | TCCACTAGCAATCTA[C/T]TTATACCATATCTTG | 245492 |
rs29121554 | snp | A/G | 0.231111 | 0.249285 | intron-variant | 4930595M18Rik | Mm_Celera | X:81469532 | CCAAGATGGTCGCTC[A/G]GTCCTGCCCGCCAGA | 245492 |
rs29121555 | snp | A/C | 0.231111 | 0.249285 | intron-variant | 4930595M18Rik | Mm_Celera | X:81469343 | GGCTGACCTGCTTGC[A/C]AAACAGGCTGCCCAA | 245492 |
rs29121556 | snp | C/T | 0.498615 | 0.0262793 | intron-variant | 4930595M18Rik | Mm_Celera | X:81469135 | CAGACAGCAGGTATT[C/T]TTTCGCCACCGCTCA | 245492 |
rs29121558 | snp | C/T | 0.124444 | 0.216185 | intron-variant | 4930595M18Rik | Mm_Celera | X:81469042 | GCTTGCCTAAAGAGA[C/T]GACAGCCCAGAGAGC | 245492 |
rs29121559 | snp | A/G | 0.498615 | 0.0262793 | intron-variant | 4930595M18Rik | Mm_Celera | X:81468981 | GAAGGAAATCAAAAA[A/G]CAGGGGCAGCAGTGG | 245492 |
rs29121560 | snp | G/T | 0.231111 | 0.249285 | intron-variant | 4930595M18Rik | Mm_Celera | X:81468974 | TTTGGATGAAGGAAA[G/T]CAAAAAGCAGGGGCA | 245492 |
rs29121561 | snp | G/T | 0.132653 | 0.220748 | intron-variant | 4930595M18Rik | Mm_Celera | X:81468937 | CAGGCTGCCCCAACT[G/T]GTGCACAGATGGTAG | 245492 |
rs29121562 | snp | C/T | 0.231111 | 0.249285 | intron-variant | 4930595M18Rik | Mm_Celera | X:81468915 | CTAGGAAAGACCTCA[C/T]TGTGGTCAGGCTGCC | 245492 |
rs29121563 | snp | A/T | 0.231111 | 0.249285 | intron-variant | 4930595M18Rik | Mm_Celera | X:81468876 | TACACCAGTGTATGG[A/T]CATCCTGGTAGAAGA | 245492 |
rs29121784 | snp | C/T | 0.124444 | 0.216185 | intron-variant | 4930595M18Rik | Mm_Celera | X:81430003 | AGGAAGTGGTCCTTT[C/T]TGGCTGATGGAAGCA | 245492 |
rs29121785 | snp | C/T | 0.231111 | 0.249285 | intron-variant | 4930595M18Rik | Mm_Celera | X:81429976 | TGACATGTAAGCACA[C/T]TTATATGACAAAGGA | 245492 |
rs29121786 | snp | G/T | 0.231111 | 0.249285 | intron-variant | 4930595M18Rik | Mm_Celera | X:81429950 | GTTGCCTAGAAGTTA[G/T]TTTTATGATTTGACA | 245492 |
rs29121787 | snp | A/T | 0.231111 | 0.249285 | intron-variant | 4930595M18Rik | Mm_Celera | X:81429906 | ATGGAGGCTGTGATA[A/T]TCATAACTATGAAGT | 245492 |
rs29121788 | snp | A/G | 0.231111 | 0.249285 | intron-variant | 4930595M18Rik | Mm_Celera | X:81429881 | AGTTTAGAAGGACCA[A/G]AAAACTAATATGGAG | 245492 |
rs29121789 | snp | A/G | 0.231111 | 0.249285 | intron-variant | 4930595M18Rik | Mm_Celera | X:81429684 | GGTTGGTATGAAAGA[A/G]AAAACAGTCAGAGGA | 245492 |
rs29121790 | snp | A/C | 0.231111 | 0.249285 | intron-variant | 4930595M18Rik | Mm_Celera | X:81429639 | TACACTAGTGAAAGC[A/C]AGTGCACAATTAAGC | 245492 |
rs29121791 | snp | A/G | 0.132653 | 0.220748 | intron-variant | 4930595M18Rik | Mm_Celera | X:81429635 | GCATTACACTAGTGA[A/G]AGCAAGTGCACAATT | 245492 |
rs29121792 | snp | C/T | 0.132653 | 0.220748 | intron-variant | 4930595M18Rik | Mm_Celera | X:81429621 | AAACTATTACAGTAG[C/T]ATTACACTAGTGAAA | 245492 |
rs29121793 | snp | G/T | 0.124444 | 0.216185 | intron-variant | 4930595M18Rik | Mm_Celera | X:81429220 | GTATGTGGATCAATT[G/T]TACTGTAATAGCAAA | 245492 |
rs29121794 | snp | A/G | 0.231111 | 0.249285 | intron-variant | 4930595M18Rik | Mm_Celera | X:81468664 | CTGACAAACTGACTC[A/G]AGGACAACGAACTAT | 245492 |
rs29121795 | snp | A/C | 0.231111 | 0.249285 | intron-variant | 4930595M18Rik | Mm_Celera | X:81468568 | CTGTGGCCTACTTGT[A/C]AAAAAAATTAGACCC | 245492 |
rs29121796 | snp | C/T | 0.142012 | 0.225474 | intron-variant | 4930595M18Rik | Mm_Celera | X:81468556 | CATAGAAACGACCTG[C/T]GGCCTACTTGTCAAA | 245492 |
rs29121797 | snp | A/G | 0.132653 | 0.220748 | intron-variant | 4930595M18Rik | Mm_Celera | X:81468460 | AGCCCTAGCCCTGCC[A/G]GACTTGACTAAGCCT | 245492 |
rs29121798 | snp | C/T | 0.231111 | 0.249285 | intron-variant | 4930595M18Rik | Mm_Celera | X:81468459 | CAGCCCTAGCCCTGC[C/T]GGACTTGACTAAGCC | 245492 |
rs29121799 | snp | C/T | 0.244898 | 0.249948 | intron-variant | 4930595M18Rik | Mm_Celera | X:81468297 | GGGAATTTCTGGTTA[C/T]GGCTGGGTTTTGTGG | 245492 |
rs29121800 | snp | A/G | 0.231111 | 0.249285 | intron-variant | 4930595M18Rik | Mm_Celera | X:81468232 | GCTGACAGAAGCTCC[A/G]AAAAACACTGTGACT | 245492 |
rs29121801 | snp | C/T | 0.132653 | 0.220748 | intron-variant | 4930595M18Rik | Mm_Celera | X:81468024 | GATGAGGCCCTCCAG[C/T]GGGACTTGGCGCCGT | 245492 |
rs29121802 | snp | C/G | 0.231111 | 0.249285 | intron-variant | 4930595M18Rik | Mm_Celera | X:81468023 | TGATGAGGCCCTCCA[C/G]CGGGACTTGGCGCCG | 245492 |
rs29121803 | snp | A/G/T | 0.231111 | 0.249285 | intron-variant | 4930595M18Rik | GRCm38.p3 | X:81467922 | GTAATCTTTGCTTTC[A/G/T]AGTGGAGAGACCCAG | 245492 |
rs29122284 | snp | A/G | 0.124444 | 0.216185 | intron-variant | 4930595M18Rik | Mm_Celera | X:81426287 | AACTAAGCATATCAC[A/G]TATAGGGTTTCCTTT | 245492 |
rs29122285 | snp | C/T | 0.231111 | 0.249285 | intron-variant | 4930595M18Rik | Mm_Celera | X:81426286 | CAACTAAGCATATCA[C/T]GTATAGGGTTTCCTT | 245492 |
rs29122286 | snp | A/T | 0.244898 | 0.249948 | intron-variant | 4930595M18Rik | Mm_Celera | X:81426194 | ATGTTTCTGTCCAAG[A/T]TGGGCATTGTTTTTG | 245492 |
rs29122287 | snp | G/T | 0.231111 | 0.249285 | intron-variant | 4930595M18Rik | Mm_Celera | X:81426117 | TAATGTTTTAGATTT[G/T]GGTTTTCGTAATTAT | 245492 |
rs29122288 | snp | C/G | 0.244898 | 0.249948 | intron-variant | 4930595M18Rik | Mm_Celera | X:81425870 | ATGAAGCAATCATAT[C/G]ATCACTTAATACAAC | 245492 |
rs29122289 | snp | A/C | 0.231111 | 0.249285 | intron-variant | 4930595M18Rik | Mm_Celera | X:81425702 | TGTCTATCTACTGCT[A/C]TTCTCCCATCTCTCA | 245492 |
rs29122290 | snp | G/T | 0.231111 | 0.249285 | intron-variant | 4930595M18Rik | Mm_Celera | X:81425676 | TGCTATTCTCACTAT[G/T]ATTTCTCTATTGTCT | 245492 |
rs29122291 | snp | C/T | 0.231111 | 0.249285 | intron-variant | 4930595M18Rik | Mm_Celera | X:81425580 | TTCAAATCTCCCACA[C/T]AGTTCTTTTGGCCCT | 245492 |
rs29122292 | snp | A/T | 0.231111 | 0.249285 | intron-variant | 4930595M18Rik | Mm_Celera | X:81425517 | ATTTTCATCATATTA[A/T]GGTCCATGTTGGCCT | 245492 |
rs29122293 | snp | C/T | 0.444444 | 0.157135 | intron-variant | 4930595M18Rik | Mm_Celera | X:81425478 | AGGCACATACTACTC[C/T]CCAATTAGCATATAC | 245492 |
rs29122334 | snp | C/G | 0.231111 | 0.249285 | intron-variant | 4930595M18Rik | Mm_Celera | X:81467839 | TCCCACCCTGACAGA[C/G]AATGGTATAAGGTAC | 245492 |
rs29122335 | snp | A/G | 0.32 | 0.24 | intron-variant | 4930595M18Rik | Mm_Celera | X:81467691 | TTTGTCAGTCTCCCT[A/G]GAATACTCAGTTGCT | 245492 |
rs29122337 | snp | A/G | 0.132653 | 0.220748 | intron-variant | 4930595M18Rik | Mm_Celera | X:81467588 | GGTGCGACTCCTATC[A/G]GGGTACGACAATACC | 245492 |
rs29122338 | snp | A/G | 0.231111 | 0.249285 | intron-variant | 4930595M18Rik | Mm_Celera | X:81466170 | CTTTTCAAACTCCAA[A/G]TTCTGGAGTCCATTA | 245492 |
rs29122339 | snp | A/T | 0.444444 | 0.157135 | intron-variant | 4930595M18Rik | Mm_Celera | X:81466044 | TATAATGCAGAAAAA[A/T]ATGCTTCTTTTGTTG | 245492 |
rs29122340 | snp | A/C | 0.231111 | 0.249285 | intron-variant | 4930595M18Rik | Mm_Celera | X:81465599 | CAGTTGAAGGTAGGG[A/C]TCACAGGCCACTCCT | 245492 |
rs29122341 | snp | C/T | 0.231111 | 0.249285 | intron-variant | 4930595M18Rik | Mm_Celera | X:81465573 | ATATAATGGTGGTCA[C/T]AGTGGAGACACAGTT | 245492 |
rs29122342 | snp | A/C/T | 0.231111 | 0.249285 | intron-variant | 4930595M18Rik | Mm_Celera | X:81465483 | AAATTATCTATAAAG[A/C/T]TAAGTTTCCTCAAGA | 245492 |
rs29122343 | snp | C/T | 0.231111 | 0.249285 | intron-variant | 4930595M18Rik | Mm_Celera | X:81465344 | CATTTTGACTTCTTG[C/T]TTTAATATACAATAA | 245492 |
rs29122774 | snp | A/T | 0.231111 | 0.249285 | intron-variant | 4930595M18Rik | Mm_Celera | X:81425369 | ATACTATAGGAGGAT[A/T]TTTAGCAGTTAGATA | 245492 |
rs29122775 | snp | C/G | 0.231111 | 0.249285 | intron-variant | 4930595M18Rik | Mm_Celera | X:81425335 | AGGCAGTCCAAATAT[C/G]GTGAAATCAGCTCAA | 245492 |
rs29122776 | snp | G/T | 0.231111 | 0.249285 | intron-variant | 4930595M18Rik | Mm_Celera | X:81425309 | GAAATACAAATGACC[G/T]GATCTCCAAAAGGCA | 245492 |
rs29122777 | snp | A/G | 0.231111 | 0.249285 | intron-variant | 4930595M18Rik | Mm_Celera | X:81423703 | TTGTTTTTCAGTATC[A/G]GCAATACATAATTTA | 245492 |
rs29122778 | snp | A/T | 0.142012 | 0.225474 | intron-variant | 4930595M18Rik | Mm_Celera | X:81423656 | CACAATGAGAAAGCA[A/T]TATAAATTCTATGCA | 245492 |
rs29122779 | snp | G/T | 0.231111 | 0.249285 | intron-variant | 4930595M18Rik | Mm_Celera | X:81423617 | GTTTTAATCACCTTT[G/T]CATAAGAATAATAAT | 245492 |
rs29122780 | snp | G/T | 0.32 | 0.24 | intron-variant | 4930595M18Rik | Mm_Celera | X:81423419 | ATAGCTGTTTAAGCA[G/T]ATTGGGATGTGAAGA | 245492 |
rs29122781 | snp | A/T | 0.132653 | 0.220748 | intron-variant | 4930595M18Rik | Mm_Celera | X:81423229 | AAAAAAAGTGACATG[A/T]TTATCCTGAAAGGCT | 245492 |
rs29122782 | snp | A/G | 0.231111 | 0.249285 | intron-variant | 4930595M18Rik | Mm_Celera | X:81423156 | AATCAGGGATAGTAG[A/G]AGAGCAGCTATCTGA | 245492 |
rs29122783 | snp | A/G | 0.132653 | 0.220748 | intron-variant | 4930595M18Rik | Mm_Celera | X:81423063 | GTGCTTTGAAATTTC[A/G]CTACGAAAGAGTAAT | 245492 |
rs29122814 | snp | C/T | 0.231111 | 0.249285 | intron-variant | 4930595M18Rik | Mm_Celera | X:81465227 | ATAAGGTTCTCAGGA[C/T]AATTGAGGGTATAAC | 245492 |
rs29122815 | snp | C/T | 0.124444 | 0.216185 | intron-variant | 4930595M18Rik | Mm_Celera | X:81465150 | CCCAGCCTCTCTTGA[C/T]ACCCGGTTCTCAGGC | 245492 |
rs29122816 | snp | A/G | 0.486111 | 0.0821678 | intron-variant | 4930595M18Rik | Mm_Celera | X:81465112 | TCATTTGTTCCAAAT[A/G]TCTATGAATTTGAGA | 245492 |
rs29122817 | snp | A/G | 0.260355 | 0.249785 | intron-variant | 4930595M18Rik | Mm_Celera | X:81465050 | GAATATGTTTAAACT[A/G]TAAGAAATAAAGACA | 245492 |
rs29122818 | snp | A/G | 0.231111 | 0.249285 | intron-variant | 4930595M18Rik | Mm_Celera | X:81464951 | AGTTATAGCTTAGAA[A/G]TTTGTACTAAATGCA | 245492 |
rs29122819 | snp | A/C | 0.231111 | 0.249285 | intron-variant | 4930595M18Rik | Mm_Celera | X:81464909 | GGAGAGAGATAAAGT[A/C]TGGGCTTTCAATATA | 245492 |
rs29122820 | snp | A/T | 0.231111 | 0.249285 | intron-variant | 4930595M18Rik | Mm_Celera | X:81464630 | ATACAGTAAGTAGAG[A/T]TATATAGTGAGTAAA | 245492 |
rs29122821 | snp | A/C | 0.492188 | 0.0620098 | intron-variant | 4930595M18Rik | Mm_Celera | X:81463172 | ATGATCTGTTCTGAA[A/C]AAATGAATACAGAAA | 245492 |
rs29122822 | snp | G/T | 0.475309 | 0.108333 | intron-variant | 4930595M18Rik | Mm_Celera | X:81462863 | CATAATGATGGTTGA[G/T]TGACCCAATTTTTAA | 245492 |
rs29122823 | snp | C/T | 0.475309 | 0.108333 | intron-variant | 4930595M18Rik | Mm_Celera | X:81462832 | TATGCATATAATCTG[C/T]ACTAGGCTATTCCTA | 245492 |
rs29123224 | snp | C/T | 0.231111 | 0.249285 | intron-variant | 4930595M18Rik | Mm_Celera | X:81423062 | TGTGCTTTGAAATTT[C/T]GCTACGAAAGAGTAA | 245492 |
rs29123225 | snp | A/C | 0.132653 | 0.220748 | intron-variant | 4930595M18Rik | Mm_Celera | X:81422982 | ACAAAGGATTGCCTA[A/C]ACCAGTTACCATCAA | 245492 |
rs29123226 | snp | A/T | 0.475309 | 0.108333 | intron-variant | 4930595M18Rik | Mm_Celera | X:81422416 | TGGAAAAGCCTAAAA[A/T]CCCCCTATAATTTGC | 245492 |
rs29123227 | snp | C/T | 0.132653 | 0.220748 | intron-variant | 4930595M18Rik | Mm_Celera | X:81422325 | TTTACAATTTATAGT[C/T]CAGAAAAACTAAAAT | 245492 |
rs29123228 | snp | A/C | 0.231111 | 0.249285 | intron-variant | 4930595M18Rik | Mm_Celera | X:81421976 | GGACTGTATGGTAAG[A/C]TGACTAAAAGCATTC | 245492 |
rs29123229 | snp | C/G | 0.260355 | 0.249785 | intron-variant | 4930595M18Rik | Mm_Celera | X:81421446 | ACTAATATAAACAAA[C/G]AAAATACACCTAAAA | 245492 |
rs29123230 | snp | A/G/T | 0.231111 | 0.249285 | intron-variant | 4930595M18Rik | Mm_Celera | X:81421186 | GCTTCAAAAGAGAAT[A/G/T]AAAACAAACACCTAC | 245492 |
rs29123231 | snp | G/T | 0.231111 | 0.249285 | missense | 4930595M18Rik | Mm_Celera | X:81420978 | TGAGTTACCCTGACA[G/T]TTTGCTGTCCAAAAC | 245492 |
rs29123232 | snp | C/T | 0.497778 | 0.0332592 | missense | 4930595M18Rik | Mm_Celera | X:81420739 | ATGTCTGGAGTCTTT[C/T]GTCTAGTACTTGTTT | 245492 |
rs29123233 | snp | C/G | 0.231111 | 0.249285 | missense | 4930595M18Rik | Mm_Celera | X:81420733 | GTCAGAATGTCTGGA[C/G]TCTTTCGTCTAGTAC | 245492 |
rs29123244 | snp | C/T | 0.493827 | 0.0552116 | intron-variant | 4930595M18Rik | Mm_Celera | X:81462680 | CATGTAGTCATGCTC[C/T]TCCTTACTTAAGATA | 245492 |
rs29123245 | snp | A/C | 0.231111 | 0.249285 | intron-variant | 4930595M18Rik | Mm_Celera | X:81462522 | TAGTCAGAAATTTTT[A/C]GTTATCCATGGTCAG | 245492 |
rs29123246 | snp | A/C | 0.492188 | 0.0620098 | intron-variant | 4930595M18Rik | Mm_Celera | X:81461579 | CTTAGTTTTGAAAAA[A/C]ATATCCAAATTATAA | 245492 |
rs29123247 | snp | A/G | 0.124444 | 0.216185 | intron-variant | 4930595M18Rik | Mm_Celera | X:81461543 | ATGTTACACACATGT[A/G]TTCTGATGCTTTCTG | 245492 |
rs29123248 | snp | C/G | 0.493827 | 0.0552116 | intron-variant | 4930595M18Rik | Mm_Celera | X:81461493 | AGTATGTTATGTACA[C/G]AAATCTTTATTTTAC | 245492 |
rs29123249 | snp | C/T | 0.124444 | 0.216185 | intron-variant | 4930595M18Rik | Mm_Celera | X:81461378 | AGATCTGCTTGTCTC[C/T]TTCTTTTGAATGCTG | 245492 |
rs29123250 | snp | A/G | 0.32 | 0.24 | intron-variant | 4930595M18Rik | Mm_Celera | X:81461193 | TGTTTTTAGTGAAGC[A/G]GATTTTCTTCAGAGG | 245492 |
rs29123251 | snp | G/T | 0.132653 | 0.220748 | intron-variant | 4930595M18Rik | Mm_Celera | X:81461066 | AATGTAGGAGCATTT[G/T]TACAGTGAAAGGAAA | 245492 |
rs29123252 | snp | A/C | 0.473373 | 0.11227 | intron-variant | 4930595M18Rik | Mm_Celera | X:81461012 | TGAATGAGAGATTAC[A/C]TAACAGTGGAAAAAT | 245492 |
rs29123253 | snp | A/C | 0.244898 | 0.249948 | intron-variant | 4930595M18Rik | Mm_Celera | X:81460979 | AGCTTTGATTTTCTC[A/C]ACAATAACTTGGAAA | 245492 |
rs29123684 | snp | C/T | 0.124444 | 0.216185 | synonymous-codon | 4930595M18Rik | Mm_Celera | X:81420570 | TAAATTGTCTCTCAA[C/T]GGTAAAAATGTGTGA | 245492 |
rs29123685 | snp | C/T | 0.46875 | 0.121031 | missense | 4930595M18Rik | Mm_Celera | X:81420560 | CAGATATGGCTAAAT[C/T]GTCTCTCAATGGTAA | 245492 |
rs29123686 | snp | C/T | 0.231111 | 0.249285 | missense | 4930595M18Rik | Mm_Celera | X:81420376 | TCAGAAATTTGTATA[C/T]CTGTCTGGTTAGAAC | 245492 |
rs29123687 | snp | A/T | 0.231111 | 0.249285 | missense | 4930595M18Rik | Mm_Celera | X:81420265 | TTATCATCTACCTCA[A/T]AAACTCCTAGCATGA | 245492 |