SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs6261555 | snp | C/T | 0.304688 | 0.243945 | synonymous-codon | N4bp2 | Mm_Celera | 5:65806379 | GGGTGACGTGAGTCA[C/T]GGTGGTCATAACCCC | 333789 |
rs6261610 | snp | C/T | 0.5 | 0 | missense | N4bp2 | Mm_Celera | 5:65806411 | TCTTTCAGGAAGCCC[C/T]GAGCACCTATTTTCC | 333789 |
rs6262226 | snp | C/T | 0.415225 | 0.187619 | synonymous-codon | N4bp2 | Mm_Celera | 5:65806559 | TGGGCGCTGTGCTGA[C/T]GATAATCAAGAAGCC | 333789 |
rs29508862 | snp | A/C | 0.497778 | 0.0332592 | intron-variant | N4bp2 | Mm_Celera | 5:65823449 | ACTGCTGAAGTGTTG[A/C]CTGCCACATGGCTTC | 333789 |
rs29511363 | snp | C/T | 0.444444 | 0.157135 | intron-variant | N4bp2 | Mm_Celera | 5:65820769 | CCCCTCCCCTTTCCT[C/T]TCCTCTCCTCTTCTC | 333789 |
rs29519365 | snp | C/T | 0.444444 | 0.157135 | intron-variant | N4bp2 | Mm_Celera | 5:65776589 | AGGCCTATTTTTCCC[C/T]CTGTTATTTTATTTG | 333789 |
rs29527203 | snp | A/G | 0.497041 | 0.0383476 | intron-variant | N4bp2 | Mm_Celera | 5:65821460 | CAGGGGTTAACTAGA[A/G]ACTGTTTTAAAGGGA | 333789 |
rs29540944 | snp | G/T | 0.415225 | 0.187619 | intron-variant | N4bp2 | Mm_Celera | 5:65772741 | AGGTACTTTGTGAGA[G/T]TGAGAATATTATTGA | 333789 |
rs29546389 | snp | C/T | 0.5 | 0 | intron-variant | N4bp2 | Mm_Celera | 5:65780076 | CCCTACATATGTACC[C/T]ACACCTGGAGTTAAA | 333789 |
rs29548261 | snp | C/T | 0.48 | 0.0979796 | intron-variant | N4bp2 | Mm_Celera | 5:65768863 | CAGTCCAGCTGGCTT[C/T]ATGCTCAAAAATATC | 333789 |
rs29561066 | snp | A/T | 0.387812 | 0.208586 | intron-variant | N4bp2 | Mm_Celera | 5:65770151 | CTATCCTCAAACCAG[A/T]GAGTTCAGAGGCTCG | 333789 |
rs29561177 | snp | C/T | 0.5 | 0 | intron-variant | N4bp2 | Mm_Celera | 5:65818078 | CAAGTGCTCTTAACC[C/T]CGAACCGTCTCCACA | 333789 |
rs29567017 | snp | A/G | 0.444444 | 0.157135 | intron-variant | N4bp2 | Mm_Celera | 5:65795468 | AAGCACACATCCTGT[A/G]CAGTGGGGAAACCAA | 333789 |
rs29568253 | snp | G/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | N4bp2 | GRCm38.p3 | 5:65775438 | TGGGAGGCAGAGACA[G/T]GTGGATCTCTGTGAG | 333789 |
rs29581957 | snp | C/G | 0.444444 | 0.157135 | upstream-variant-2KB | N4bp2 | Mm_Celera | 5:65761597 | CATCTGTAAAATCTA[C/G]AATTAAGCAGAGGGA | 333789 |
rs29583558 | snp | G/T | 0.444444 | 0.157135 | intron-variant | N4bp2 | Mm_Celera | 5:65822792 | TAATGCTGTAATCTC[G/T]CGGCTACTGAGTACC | 333789 |
rs29584991 | snp | A/G | 0.5 | 0 | intron-variant | N4bp2 | GRCm38.p3 | 5:65779934 | TCAGGGCCCTAGCAT[A/G]TTTATACCCTCTGAA | 333789 |
rs29586742 | snp | C/T | 0.484429 | 0.0868505 | intron-variant | N4bp2 | Mm_Celera | 5:65823717 | TGATTAAGGCTTTTC[C/T]GCACACGGCTCAGCA | 333789 |
rs29627694 | snp | C/T | 0.5 | 0 | intron-variant | N4bp2 | Mm_Celera | 5:65780145 | AAGAAACCAAAATTC[C/T]AGAATTGCATTACAG | 333789 |
rs29630657 | snp | A/G | 0.444444 | 0.157135 | intron-variant, upstream-variant-2KB | N4bp2 | Mm_Celera | 5:65774310 | TTGACTGGAGGAAGG[A/G]GTAGACCTTGGTTTC | 333789 |
rs29633223 | snp | A/G | 0.5 | 0 | intron-variant | N4bp2 | Mm_Celera | 5:65817058 | GGGAACCAAACCTGC[A/G]TTCTCTGCAAAAGCA | 333789 |
rs29683854 | snp | A/G | 0.429688 | 0.173817 | intron-variant | N4bp2 | Mm_Celera | 5:65821982 | AAAACAGAAGGTAGG[A/G]ATGTGCTCGTGACAT | 333789 |
rs29684850 | snp | A/G | 0.5 | 0 | intron-variant | N4bp2 | Mm_Celera | 5:65821337 | CTGATGCTGGGTTAG[A/G]GCATATACAGATATG | 333789 |
rs29685047 | snp | A/T | 0.444444 | 0.157135 | intron-variant, upstream-variant-2KB | N4bp2 | GRCm38.p3 | 5:65774496 | TTTTTCGAGACAGGG[A/T]TTCTCTGTGTAGCCC | 333789 |
rs29728283 | snp | C/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | N4bp2 | Mm_Celera | 5:65774018 | AGAGGGCATCAGATC[C/T]CATTACAGATGGTTG | 333789 |
rs29729598 | snp | C/T | 0.444444 | 0.157135 | intron-variant | N4bp2 | Mm_Celera | 5:65777940 | CTTCAGAAGAGCAGT[C/T]GGGTGCTCTTACCCA | 333789 |
rs29734309 | snp | A/G | 0.5 | 0 | intron-variant | N4bp2 | Mm_Celera | 5:65777180 | TATGGGTCAGTGACC[A/G]GGGAGACTAATCATG | 333789 |
rs29771388 | snp | A/G | 0.375 | 0.216506 | intron-variant | N4bp2 | Mm_Celera | 5:65778053 | ACAACCAATATGTGT[A/G]TATATATATATATAT | 333789 |
rs29771550 | snp | C/T | 0.444444 | 0.157135 | intron-variant | N4bp2 | Mm_Celera | 5:65813436 | GAATTTAAAAGAAGA[C/T]ACTCTAAGAATTCCA | 333789 |
rs29780618 | snp | A/T | 0.444444 | 0.157135 | intron-variant | N4bp2 | Mm_Celera | 5:65813523 | CCCCTCAACATCACC[A/T]TAAAAGCTTTTTAAG | 333789 |
rs29781222 | snp | C/T | 0.497041 | 0.0383476 | intron-variant | N4bp2 | Mm_Celera | 5:65775841 | GTGCCCTAGTTTTTC[C/T]ATTTAGTGACTGTTT | 333789 |
rs33057252 | snp | A/G | 0.5 | 0 | intron-variant | N4bp2 | GRCm38.p3 | 5:65779940 | CCCTAGCATATTTAT[A/G]CCCTCTGAAAATTTC | 333789 |
rs33081128 | snp | C/G | 0.473373 | 0.11227 | intron-variant | N4bp2 | Mm_Celera | 5:65813842 | CATCATAAACATTTG[C/G]AACTCTGCTCTGCTG | 333789 |
rs33134101 | snp | C/T | 0.5 | 0 | intron-variant | N4bp2 | Mm_Celera | 5:65769394 | CCTGTGCACTAACTA[C/T]TTACTAACAGTCTCC | 333789 |
rs33142282 | snp | C/T | 0.5 | 0 | intron-variant | N4bp2 | Mm_Celera | 5:65776909 | GAGCGTGGAAATAGT[C/T]AGCTGTAGTGGATGA | 333789 |
rs33144291 | snp | C/T | 0.48 | 0.0979796 | intron-variant | N4bp2 | Mm_Celera | 5:65779559 | TGGTTCCATTTATAC[C/T]GTGGCCCTGAATAGG | 333789 |
rs33169955 | snp | G/T | 0.359862 | 0.224567 | intron-variant | N4bp2 | Mm_Celera | 5:65771750 | TAGAAGCACCTGATA[G/T]ATGTAGATAGATGCA | 333789 |
rs33183648 | snp | C/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | N4bp2 | Mm_Celera | 5:65775341 | TATACTCCCAAATGT[C/T]TAATCTATTTTAGAT | 333789 |
rs33191656 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | N4bp2 | Mm_Celera | 5:65818862 | ACTCAGGTGGGAAGC[A/G]TATGGACGTTTGTAT | 333789 |
rs33205506 | snp | A/G | 0.456747 | 0.140554 | intron-variant | N4bp2 | Mm_Celera | 5:65768041 | GTGGGTTATGACACC[A/G]ACAAGTCAGCTGGAT | 333789 |
rs33210366 | snp | C/T | 0.444444 | 0.157135 | intron-variant | N4bp2 | GRCm38.p3 | 5:65777920 | CTGGGAATTGAACTT[C/T]GGACCTTCAGAAGAG | 333789 |
rs33237629 | snp | C/T | 0.444444 | 0.157135 | intron-variant | N4bp2 | Mm_Celera | 5:65776432 | GTAAGGCCACACCCC[C/T]TAATAGTGCCACTCT | 333789 |
rs33251848 | snp | A/T | 0.5 | 0 | intron-variant | N4bp2 | Mm_Celera | 5:65817935 | TACATGCATGTATGT[A/T]TATCTGTGTGCAGGG | 333789 |
rs33270681 | snp | A/G | 0.444444 | 0.157135 | intron-variant | N4bp2 | Mm_Celera | 5:65820150 | TAGGATTACAGACAT[A/G]TACCACCATGCCTGG | 333789 |
rs33287715 | snp | C/T | 0.429688 | 0.173817 | intron-variant | N4bp2 | Mm_Celera | 5:65820029 | GCCAGAGTAACCCAG[C/T]TTCTGTGTAGCCAGG | 333789 |
rs33301303 | snp | G/T | 0.5 | 0 | intron-variant | N4bp2 | Mm_Celera | 5:65788722 | TTCCCTTAGAAAACA[G/T]TGTGGCTGACTGTCA | 333789 |
rs33318735 | snp | C/T | 0.48 | 0.0979796 | intron-variant | N4bp2 | Mm_Celera | 5:65823599 | AGAGACAATATATCA[C/T]TAAGTTGCCCAGGCT | 333789 |
rs33338794 | snp | A/T | 0.444444 | 0.157135 | intron-variant | N4bp2 | Mm_Celera | 5:65813524 | CCCTCAACATCACCA[A/T]AAAAGCTTTTTAAGA | 333789 |
rs33354155 | snp | C/T | 0.5 | 0 | intron-variant | N4bp2 | Mm_Celera | 5:65770968 | GACATTTTCTAAGCC[C/T]GACATATAATTTACA | 333789 |
rs33379886 | snp | A/T | 0.444444 | 0.157135 | intron-variant, upstream-variant-2KB | N4bp2 | Mm_Celera | 5:65773844 | GCTGGTCATATGCAC[A/T]TATGAATATATATGT | 333789 |
rs33393717 | snp | A/G | 0.444444 | 0.157135 | intron-variant | N4bp2 | Mm_Celera | 5:65823565 | CACTACTGAATTATA[A/G]AGGAGTTGTTTGGGT | 333789 |
rs33399303 | snp | A/T | 0.486111 | 0.0821678 | intron-variant | N4bp2 | Mm_Celera | 5:65777315 | GGAACAAGAGCTACA[A/T]GCTGCTCAGCTACAC | 333789 |
rs33412281 | snp | C/T | 0.5 | 0 | intron-variant | N4bp2 | Mm_Celera | 5:65782326 | TTTTCTTAGACCCTG[C/T]GCCCCACTCCCCAAC | 333789 |
rs33439564 | snp | A/G | 0.5 | 0 | intron-variant | N4bp2 | Mm_Celera | 5:65780344 | AAAAAGAGGGAAGGG[A/G]CCAGAGCGGTAGCTC | 333789 |
rs33442420 | snp | C/T | 0.48 | 0.0979796 | intron-variant | N4bp2 | Mm_Celera | 5:65769385 | TCATTCTTTCCTGTG[C/T]ACTAACTACTTACTA | 333789 |
rs33447791 | snp | A/G | 0.5 | 0 | intron-variant | N4bp2 | Mm_Celera | 5:65822019 | TGCCAAACACAGTGA[A/G]TCTGCCTGAGCAGAC | 333789 |
rs33461309 | snp | C/T | 0.5 | 0 | intron-variant | N4bp2 | Mm_Celera | 5:65770982 | CCGACATATAATTTA[C/T]ATCCTTTCAGTTTTC | 333789 |
rs33493310 | snp | C/G | 0.429688 | 0.173817 | intron-variant, upstream-variant-2KB | N4bp2 | Mm_Celera | 5:65775091 | CTCAAGGTCATGGAT[C/G]GAGCATGGGGAAGGG | 333789 |
rs33495855 | snp | C/T | 0.444444 | 0.157135 | upstream-variant-2KB, utr-variant-5-prime | N4bp2 | Mm_Celera | 5:65763401 | GCTGGGGCCGCGGGG[C/T]CCTTTGTTCCCGCGG | 333789 |
rs33506311 | snp | A/T | 0.48 | 0.0979796 | intron-variant | N4bp2 | GRCm38.p3 | 5:65815058 | TGTTAATTAAAATTT[A/T]AAAAAAAAAATCGTT | 333789 |
rs33506477 | snp | A/T | 0.5 | 0 | intron-variant | N4bp2 | Mm_Celera | 5:65814084 | GTCTGTTAAGAGGAC[A/T]CATGGGAGACATTTC | 333789 |
rs33508933 | snp | A/G | 0.444444 | 0.157135 | intron-variant, upstream-variant-2KB | N4bp2 | Mm_Celera | 5:65775022 | CGCTGCTAAGTCAGG[A/G]ATAGGCTCAGGTTGG | 333789 |
rs33545517 | snp | A/G | 0.5 | 0 | intron-variant | N4bp2 | Mm_Celera | 5:65822086 | CTGCCTCTGCTTCCA[A/G]AAGGCTAGGATTAAA | 333789 |
rs33552257 | snp | A/G | 0.5 | 0 | intron-variant | N4bp2 | Mm_Celera | 5:65772671 | AACCGCAGTGAGTGA[A/G]GGAGAGAATCTGGAT | 333789 |
rs33557989 | snp | C/T | 0.5 | 0 | upstream-variant-2KB | N4bp2 | Mm_Celera | 5:65761306 | CTGAGGCTTCACACA[C/T]GAGACAAGAACAGTA | 333789 |
rs33561886 | snp | G/T | 0.401235 | 0.199068 | intron-variant | N4bp2 | Mm_Celera | 5:65772803 | AAACTTTGAGATGGT[G/T]TGGGTATAGAGCATA | 333789 |
rs33568557 | snp | C/T | 0.493827 | 0.0552116 | intron-variant | N4bp2 | Mm_Celera | 5:65818229 | GTACTGAGATTAAAG[C/T]TGTGGGTCACCATGC | 333789 |
rs33576548 | snp | C/G | 0.498615 | 0.0262793 | intron-variant | N4bp2 | Mm_Celera | 5:65824797 | CATACTAAAATTTTA[C/G]AGTGCTTCATTAATA | 333789 |
rs33590837 | snp | A/G | 0.48 | 0.0979796 | intron-variant | N4bp2 | Mm_Celera | 5:65779987 | CACACAATCACAGAA[A/G]TGATCTGCAGCTGGC | 333789 |
rs33591506 | snp | A/G | 0.492188 | 0.0620098 | intron-variant, upstream-variant-2KB | N4bp2 | Mm_Celera | 5:65775214 | ATAGTATCTTACTTA[A/G]AATAAATGCTTAGCT | 333789 |
rs33599341 | snp | A/G | 0.432133 | 0.171253 | missense | N4bp2 | Mm_Celera | 5:65825283 | ACAGAATTTAAACAG[A/G]GTGGTGGCAAGCCGT | 333789 |
rs33642592 | snp | A/G | 0.5 | 0 | intron-variant | N4bp2 | Mm_Celera | 5:65769095 | TTGGGAAGATGGGGC[A/G]GGGGCGGGGGGGCGG | 333789 |
rs33645178 | snp | C/T | 0.444444 | 0.157135 | intron-variant | N4bp2 | Mm_Celera | 5:65768375 | TAAGAAGTCTGAAGC[C/T]TAGAAATAATTCTGT | 333789 |
rs33648902 | snp | A/G | 0.5 | 0 | intron-variant | N4bp2 | Mm_Celera | 5:65777062 | AGGGTCTGCCCAAGT[A/G]GTGTAGGGAGCATGG | 333789 |
rs33655794 | snp | A/T | 0.32 | 0.24 | intron-variant | N4bp2 | Mm_Celera | 5:65768849 | CTACATTGCCCTGGC[A/T]GTCCAGCTGGCTTCA | 333789 |
rs33662086 | snp | G/T | 0.475309 | 0.108333 | intron-variant, upstream-variant-2KB | N4bp2 | Mm_Celera | 5:65774187 | CTGCGAACTGGGATG[G/T]CAGATGTAGTGTCAT | 333789 |
rs33662595 | snp | C/T | 0.465374 | 0.126941 | utr-variant-5-prime | N4bp2 | Mm_Celera | 5:65775605 | AGACTGCTGTAGAGT[C/T]GCAGATGACAATCTT | 333789 |
rs33671572 | snp | C/T | 0.444444 | 0.157135 | intron-variant | N4bp2 | Mm_Celera | 5:65776609 | TATTTTATTTGGGGT[C/T]TTTTATTTATACCTC | 333789 |
rs33683771 | snp | A/G | 0.5 | 0 | intron-variant | N4bp2 | Mm_Celera | 5:65785249 | GGTCCCAGTGGGAGG[A/G]GAAACATTGGAGGAG | 333789 |
rs33708757 | snp | C/T | 0.5 | 0 | intron-variant | N4bp2 | Mm_Celera | 5:65779209 | AAGTTCACTTTTAAT[C/T]ACTCACATGATGGCT | 333789 |
rs33719800 | snp | C/G | 0.444444 | 0.157135 | intron-variant | N4bp2 | Mm_Celera | 5:65782059 | CATTTCTAATATAAA[C/G]AACTATAGATCGGGG | 333789 |
rs33732622 | snp | G/T | 0.5 | 0 | intron-variant | N4bp2 | Mm_Celera | 5:65779449 | TAGCTTTATGCTCAG[G/T]AACAAATGAATGAAG | 333789 |
rs33734278 | snp | A/G | 0.48 | 0.0979796 | intron-variant | N4bp2 | Mm_Celera | 5:65823657 | AACTCTGTAACACAG[A/G]TTGACCTTGAACTTA | 333789 |
rs33739040 | snp | C/T | 0.5 | 0 | intron-variant | N4bp2 | Mm_Celera | 5:65775970 | ATACCCAAGATCTGC[C/T]GGCCTGCTTCTGCTT | 333789 |
rs33753049 | snp | C/G | 0.456747 | 0.140554 | intron-variant, upstream-variant-2KB | N4bp2 | Mm_Celera | 5:65775125 | TCAGGCCCATTACCC[C/G]GTCTAAGGAATAGTC | 333789 |
rs36242693 | snp | A/G/T | 0.244898 | 0.249948 | utr-variant-3-prime | N4bp2 | GRCm38.p3 | 5:65827414 | GGTACAATAGGTAAC[A/G/T]TTCAGAGAAGGAGAG | 333789 |
rs36252257 | snp | A/G | 0.396694 | 0.202437 | intron-variant | N4bp2 | Mm_Celera | 5:65784848 | AGTAGGAGACACATA[A/G]CTAAATATGTATGAA | 333789 |
rs36258462 | snp | A/T | 0.165289 | 0.235211 | intron-variant, upstream-variant-2KB | N4bp2 | Mm_Celera | 5:65774367 | GAGACAGAGAAGGGC[A/T]GAAGACAAGATACCC | 333789 |
rs36263376 | snp | A/T | 0.35503 | 0.226867 | intron-variant | N4bp2 | Mm_Celera | 5:65784470 | GGGACTTGACTTTGA[A/T]TTGGGTAGTCAGGGA | 333789 |
rs36270983 | snp | A/T | 0.444444 | 0.157135 | intron-variant | N4bp2 | Mm_Celera | 5:65772061 | AAGGCTTGTTATGTG[A/T]CAGAGCCCAGGAGGA | 333789 |
rs36276300 | snp | C/G | 0.132653 | 0.220748 | intron-variant | N4bp2 | Mm_Celera | 5:65798703 | TCTTGAGCCATGTGT[C/G]TACTGAAGGCAGGAC | 333789 |
rs36283786 | snp | A/G | 0.32 | 0.24 | intron-variant | N4bp2 | Mm_Celera | 5:65826114 | CTGAGAACACCAGTC[A/G]TTAAATCTCCTCTAA | 333789 |
rs36293575 | snp | A/G | 0.132653 | 0.220748 | synonymous-codon | N4bp2 | Mm_Celera | 5:65808443 | GACTCCCACGCCAGT[A/G]ACAGCCACATCTCTG | 333789 |
rs36295681 | snp | A/C | 0.124444 | 0.216185 | intron-variant | N4bp2 | Mm_Celera | 5:65766368 | CCTTTAGCTTTTCCT[A/C]TGTAGAATCATGTAA | 333789 |
rs36311181 | snp | A/C | 0.231111 | 0.249285 | intron-variant | N4bp2 | Mm_Celera | 5:65772990 | AATATCTGACTGGAA[A/C]TATGTTGAATAGCAC | 333789 |
rs36319015 | snp | A/G | 0.124444 | 0.216185 | intron-variant | N4bp2 | Mm_Celera | 5:65802740 | AAAAATATTGTTTGA[A/G]CCTAAAATGTAATAA | 333789 |
rs36321780 | snp | A/G | 0.244898 | 0.249948 | intron-variant | N4bp2 | Mm_Celera | 5:65816664 | AGATTTTTGAGCCTG[A/G]GCATAAAGTGCTTGG | 333789 |
rs36326064 | snp | C/T | 0.231111 | 0.249285 | intron-variant | N4bp2 | Mm_Celera | 5:65785946 | GAGTTATGTGGATAC[C/T]GTTCCACCTTAGGAG | 333789 |
rs36344686 | snp | A/G | 0.124444 | 0.216185 | intron-variant | N4bp2 | Mm_Celera | 5:65799198 | AGTTGCTTTGTAGTA[A/G]TTTGAACTAATTCAA | 333789 |
rs36348596 | snp | A/G | 0.32 | 0.24 | intron-variant | N4bp2 | Mm_Celera | 5:65800315 | TCCTGTGTCACTGCA[A/G]CCAGCCTCAATAGTT | 333789 |