SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs6223315 | snp | A/G | 0.5 | 0 | intron-variant | Nsmaf | Mm_Celera | 4:6410946 | gaggcagaggcaggc[A/G]gatttctgagttcga | 18201 |
rs6359912 | snp | A/T | 0.5 | 0 | intron-variant | Nsmaf | Mm_Celera | 4:6404125 | tcatctttgacaatt[A/T]gggaaatgaaaattt | 18201 |
rs6359927 | snp | A/T | 0.5 | 0 | intron-variant | Nsmaf | Mm_Celera | 4:6404142 | ggaaatgaaaattta[A/T]aacgactttgagatt | 18201 |
rs13470983 | snp | C/T | 0.132653 | 0.220748 | downstream-variant-500B, utr-variant-3-prime | Sdcbp, Nsmaf | Mm_Celera | 4:6396368 | TTCTGACGGTAACAC[C/T]GTTCTTTGATGTGCG | 18201 |
rs13470984 | snp | G/T | | | downstream-variant-500B, utr-variant-3-prime | Sdcbp, Nsmaf | GRCm38.p3 | 4:6396332 | GGACTGGTTCCTTTC[G/T]GCAGTGCTGCGTGCC | 18201 |
rs27663168 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Nsmaf | Mm_Celera | 4:6440669 | TACTTGACTGTAACC[C/T]AGTGACTGAGAGCAG | 18201 |
rs27663169 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Nsmaf | Mm_Celera | 4:6440608 | ATTATTATTACTTCA[C/T]TCTGAAGAGGGTGAC | 18201 |
rs27663170 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Nsmaf | Mm_Celera | 4:6440551 | TTACAGGAGCAATTC[A/G]AAGTCATGGAGAAAG | 18201 |
rs27663171 | snp | A/T | 0.142012 | 0.225474 | intron-variant | Nsmaf | Mm_Celera | 4:6440284 | ACCAATAAAATTGGA[A/T]GGTCACTCATGGGTC | 18201 |
rs27663172 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Nsmaf | Mm_Celera | 4:6440235 | ATCAAACATGGGCCA[C/T]ACAGAAACAAATGGC | 18201 |
rs27663173 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Nsmaf | Mm_Celera | 4:6440124 | CTCCCCTAATGGTTT[C/T]AGCAGCCCTTGGAGA | 18201 |
rs27663174 | snp | A/C | 0.244898 | 0.249948 | intron-variant | Nsmaf | Mm_Celera | 4:6440006 | TTCTGTTCCCTACTC[A/C]GGCAATGCCTCAAGG | 18201 |
rs27663175 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Nsmaf | Mm_Celera | 4:6439954 | GTGATATTCCTCTGC[C/T]GTGTCCTTCTTTACA | 18201 |
rs27663176 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Nsmaf | Mm_Celera | 4:6439836 | GTGCTTTTTGCAATA[C/G]TAGGACAGAACCCAG | 18201 |
rs27663177 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Nsmaf | Mm_Celera | 4:6439061 | CTTCCATATAAGTCT[C/T]TAAAGAAGCACCTCT | 18201 |
rs27663178 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Nsmaf | Mm_Celera | 4:6438860 | TTGCTTTTAATATGT[A/G]AACATACCCAAGAGT | 18201 |
rs27663179 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Nsmaf | Mm_Celera | 4:6438691 | CTCTCCTCTTGTGTG[A/G]AGGACGTTTGCTGGA | 18201 |
rs27663180 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Nsmaf | Mm_Celera | 4:6438409 | TTGAATCTTCACAAC[C/T]GCTCTCCACATAACC | 18201 |
rs27663181 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Nsmaf | Mm_Celera | 4:6438356 | CCCCGTGAACCCATT[A/G]ATTACTAACAATTAT | 18201 |
rs27663182 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Nsmaf | Mm_Celera | 4:6438341 | CGGGCTGAAGTGCAA[C/T]CCCGTGAACCCATTG | 18201 |
rs27663183 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Nsmaf | Mm_Celera | 4:6438268 | GCAGAGCGGTGACCA[C/T]GACGGCCACCACGAC | 18201 |
rs27663184 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Nsmaf | Mm_Celera | 4:6438222 | CTAAGGTGTCAGCTA[A/G]TCAAAGCTCAGCAGT | 18201 |
rs27663185 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Nsmaf | Mm_Celera | 4:6438159 | AGATTATCTGATGAA[C/T]ACCAAGACAACCTCA | 18201 |
rs27663186 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Nsmaf | Mm_Celera | 4:6438024 | GGAATGTTTCTGCTC[A/G]CATTCAAAACACCTT | 18201 |
rs27663187 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Nsmaf | Mm_Celera | 4:6437436 | GGAGGCCACAGAAGG[A/G]ACTGCTGTGCGCTCA | 18201 |
rs27663188 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Nsmaf | Mm_Celera | 4:6437355 | CCCCTTCCTGAGGCA[C/T]GCTGGGCTGTCATGT | 18201 |
rs27663189 | snp | A/G | 0.18 | 0.24 | intron-variant | Nsmaf | Mm_Celera | 4:6437332 | AGTCATTCCTGAGAG[A/G]AGGGACTCCCCTTCC | 18201 |
rs27663190 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Nsmaf | Mm_Celera | 4:6437308 | GGAATGAACAAAAAC[A/C]AATCCTGTAGTCATT | 18201 |
rs27663191 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Nsmaf | Mm_Celera | 4:6437293 | ATGCGGCATGCATCC[A/G]GAATGAACAAAAACA | 18201 |
rs27663192 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Nsmaf | Mm_Celera | 4:6437243 | GTGATGCCAATACTG[A/G]TTTGAGTTCAACTGT | 18201 |
rs27663193 | snp | C/T | 0.18 | 0.24 | intron-variant | Nsmaf | Mm_Celera | 4:6437184 | TTTCAGTCTACAAAC[C/T]AACTAATGATATGCC | 18201 |
rs27663194 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Nsmaf | Mm_Celera | 4:6437038 | CCCGACTGAGCACAG[A/G]ATGATGAGTGATGAC | 18201 |
rs27663195 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Nsmaf | Mm_Celera | 4:6436943 | CTTTCCCTCTACTCC[C/T]GAGATGCTCCAGGCA | 18201 |
rs27663196 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Nsmaf | Mm_Celera | 4:6436756 | GGAGCATTAAATATG[A/G]AGTTGAAGATAGTTC | 18201 |
rs27663197 | snp | A/T | 0.142012 | 0.225474 | intron-variant | Nsmaf | Mm_Celera | 4:6436150 | TTTTATTTCAGTAAA[A/T]GGTAGCCCGATCCAG | 18201 |
rs27663198 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Nsmaf | Mm_Celera | 4:6436010 | CTTTATCTTTCTGGC[C/T]TCAGCCTCATGAAAC | 18201 |
rs27663199 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Nsmaf | Mm_Celera | 4:6435813 | AGCAAGACTCTTTGC[C/T]AGAGTTATTTGTAAC | 18201 |
rs27663200 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Nsmaf | Mm_Celera | 4:6435752 | AAACAGGTAGCCACA[C/T]TGATGGTATCACACC | 18201 |
rs27663201 | snp | C/T | 0.484429 | 0.0868505 | intron-variant | Nsmaf | Mm_Celera | 4:6435352 | ATTTGTACCAAGTAG[C/T]CAATCACATAAGGCT | 18201 |
rs27663202 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Nsmaf | Mm_Celera | 4:6435238 | AGGTACCCATATTTA[C/T]ATTAGTATGGTTTTA | 18201 |
rs27663203 | snp | A/G | 0.489796 | 0.070696 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | Nsmaf | Mm_Celera | 4:6435081 | CTTATACGGTGCCAC[A/G]ATGTTGTGCTCCTTA | 18201 |
rs27663204 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Nsmaf | Mm_Celera | 4:6434404 | CCAACAAGTGCCTAC[A/G]CGTCCCTGAAAACAA | 18201 |
rs27663205 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Nsmaf | Mm_Celera | 4:6434362 | CTGCTGCAGTGGACT[A/G]AGTGCAAAGGATACC | 18201 |
rs27663206 | snp | A/G | 0.456747 | 0.140554 | intron-variant | Nsmaf | Mm_Celera | 4:6434120 | TTACACACAGTGGAT[A/G]TGAACTGCACTACAC | 18201 |
rs27663207 | snp | C/T | 0.426035 | 0.177515 | intron-variant | Nsmaf | Mm_Celera | 4:6433765 | TTAATTTCCCTCATG[C/T]ACTATGTGTACACAG | 18201 |
rs27663208 | snp | C/T | 0.197531 | 0.244432 | intron-variant | Nsmaf | Mm_Celera | 4:6433201 | AAGGGAAAACTAAAC[C/T]AAAGGTTTCCGACTG | 18201 |
rs27663209 | snp | A/G | 0.132653 | 0.220748 | synonymous-codon, nc-transcript-variant | Nsmaf | Mm_Celera | 4:6432709 | TGATGTCCTAGCCAG[A/G]CGTGACTGCAAGATA | 18201 |
rs27663210 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Nsmaf | Mm_Celera | 4:6431505 | AGTGTAGCTCTGTCT[A/G]TGTTGCTGGGACCAG | 18201 |
rs27663211 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Nsmaf | Mm_Celera | 4:6431503 | TGAGTGTAGCTCTGT[C/T]TGTGTTGCTGGGACC | 18201 |
rs27663212 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Nsmaf | Mm_Celera | 4:6431366 | AGAGAGACGGTCACA[C/G]TGGGGATGCACGGGC | 18201 |
rs27663213 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Nsmaf | Mm_Celera | 4:6428849 | GTTTTATGCCAGCAC[C/T]AGGAGGAAGCTGAGA | 18201 |
rs27663214 | snp | A/G | 0.429688 | 0.173817 | intron-variant | Nsmaf | Mm_Celera | 4:6428323 | CATAGTAACTATAAC[A/G]TCAGGTTCCTGGAAA | 18201 |
rs27663215 | snp | A/G | 0.290657 | 0.246672 | intron-variant | Nsmaf | Mm_Celera | 4:6428303 | CCTTCCCCAAGATGT[A/G]AGGGCATAGTAACTA | 18201 |
rs27663216 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Nsmaf | Mm_Celera | 4:6428179 | CTTTACGCACTACTG[A/G]GTACAAGGTCCTTCA | 18201 |
rs27663217 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Nsmaf | Mm_Celera | 4:6428094 | TTCACCACAGCCTTT[C/T]CTGGGTGTCTTACCC | 18201 |
rs27663218 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Nsmaf | Mm_Celera | 4:6428023 | ACGGAAGCCAGAGAC[C/T]CACTGTCTGCAGTGA | 18201 |
rs27663219 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Nsmaf | Mm_Celera | 4:6427894 | TAGTTTTAGGTCTAG[C/T]GTTCTCAAAGAGAAG | 18201 |
rs27663220 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Nsmaf | Mm_Celera | 4:6427755 | AGCTGTGTGGCCAGA[A/G]AGACGGGACTTGTCC | 18201 |
rs27663221 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Nsmaf | Mm_Celera | 4:6427559 | ACCAAGCCAGCCAGC[C/T]ATGTGCCATGTCATT | 18201 |
rs27663222 | snp | A/C | 0.142012 | 0.225474 | intron-variant | Nsmaf | Mm_Celera | 4:6427338 | GAGAGTCAAAATTAG[A/C]AAATATTGTATGCTT | 18201 |
rs27663223 | snp | A/T | 0.18 | 0.24 | intron-variant | Nsmaf | Mm_Celera | 4:6427277 | TTTAAAGGAAAAAAA[A/T]TTGATTCTCTGGAAC | 18201 |
rs27663224 | snp | A/C | 0.396694 | 0.202437 | intron-variant | Nsmaf | Mm_Celera | 4:6427001 | CAGGGTCTCTCCCTG[A/C]ACCTGTCTCCACCCA | 18201 |
rs27663225 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Nsmaf | Mm_Celera | 4:6426666 | CACGTTTCTAACCCT[C/T]GTCAGTAATCTCAGA | 18201 |
rs27663226 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Nsmaf | Mm_Celera | 4:6426654 | ATTTAGCTTGGACAC[A/G]TTTCTAACCCTTGTC | 18201 |
rs27663227 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Nsmaf | Mm_Celera | 4:6426276 | AGAAATGTAATTCCT[A/G]TATCAATTTCTAGCT | 18201 |
rs27663228 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Nsmaf | Mm_Celera | 4:6425932 | GTGTGCTCTGTGCAC[A/G]GTGAGGGACGTGGTG | 18201 |
rs27663229 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Nsmaf | Mm_Celera | 4:6425648 | GGAAGCCGAACCAAT[A/G]GGAATCTCGTTGCTC | 18201 |
rs27663230 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Nsmaf | Mm_Celera | 4:6425616 | CAGCTGGGCCTCGGG[C/T]CGCGGGCCGGCAGCC | 18201 |
rs27663231 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Nsmaf | Mm_Celera | 4:6425569 | CCAGCCAGGAGAGCC[C/T]GGATTCACGGCTGCT | 18201 |
rs27663232 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Nsmaf | Mm_Celera | 4:6425345 | TAAATAACCATGAAA[C/T]GTAACAAAATAATAA | 18201 |
rs27663233 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Nsmaf | Mm_Celera | 4:6425079 | GGTAAGCATCTATAC[A/G]CTTGAGTTTTCGACC | 18201 |
rs27663234 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Nsmaf | Mm_Celera | 4:6424813 | GTGTCTGTTCTCTTA[C/T]TTGCTGTCCCAGCTT | 18201 |
rs27663235 | snp | C/T | 0.207612 | 0.24638 | intron-variant | Nsmaf | Mm_Celera | 4:6424563 | ATTCACCTACACAAA[C/T]ATCCTCTCCCACCTT | 18201 |
rs27663236 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Nsmaf | Mm_Celera | 4:6424045 | CAAAACCACCTAGGC[C/T]TAATCAAGCTTTCTA | 18201 |
rs27663237 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Nsmaf | Mm_Celera | 4:6423797 | GTTCTACAGAACGTG[A/C]TGGGTTTGGACAGTT | 18201 |
rs27663238 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Nsmaf | Mm_Celera | 4:6423692 | AAGCCACTCCCAGAC[A/G]TTACATAACTTTACA | 18201 |
rs27663239 | snp | C/T | 0.42 | 0.183303 | intron-variant | Nsmaf | Mm_Celera | 4:6423269 | CTAACTAAGACAACA[C/T]GCTTCCCTTTGGAAG | 18201 |
rs27663240 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Nsmaf | Mm_Celera | 4:6422813 | ATGACCTTCGCAAAT[A/G]TGTAAATACACATAA | 18201 |
rs27663241 | snp | A/T | 0.142012 | 0.225474 | intron-variant | Nsmaf | Mm_Celera | 4:6422730 | AAACTTAAATATTTT[A/T]AAACTTGTCACTTAC | 18201 |
rs27663242 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Nsmaf | Mm_Celera | 4:6422639 | TAGTAGATGCCTGAT[C/T]ATTAATTTCCTTTTT | 18201 |
rs27663243 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Nsmaf | Mm_Celera | 4:6422264 | TAAGATGTCATTGTT[C/T]GAAAGCAGTGAAAAG | 18201 |
rs27663244 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Nsmaf | Mm_Celera | 4:6422131 | GTCTTGAGTGCCAGC[C/G]TGAGTGGCCTGGGAA | 18201 |
rs27663245 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Nsmaf | Mm_Celera | 4:6421935 | TAAACAATTGGTTAG[C/T]ACTTTTAATGACAAG | 18201 |
rs27663246 | snp | A/C | 0.152778 | 0.230321 | intron-variant | Nsmaf | Mm_Celera | 4:6421788 | TTCCAAATAAAACTC[A/C]AAAACAAATTTTAAA | 18201 |
rs27663247 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Nsmaf | Mm_Celera | 4:6421397 | GATACCCAGAATATA[A/G]GGTTTTTGGGTTTTT | 18201 |
rs27663248 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Nsmaf | Mm_Celera | 4:6421200 | GCCAAGCTCACACCT[A/G]CTTCTATAAAGTAGT | 18201 |
rs27663249 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Nsmaf | Mm_Celera | 4:6420918 | AAAGCAGAGCACACA[A/G]GAGCAGTGGTCACAG | 18201 |
rs27663250 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Nsmaf | Mm_Celera | 4:6420335 | ACAGATGTAATTTTG[C/T]GTGTAGGGAGAGGGT | 18201 |
rs27663251 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Nsmaf | Mm_Celera | 4:6420295 | TCTGATTTTCTAGGT[G/T]TTGATGGTGCTGACA | 18201 |
rs27663252 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Nsmaf | Mm_Celera | 4:6420250 | CCATTCCTGCCTTAG[G/T]AACAGCAGAGGGACA | 18201 |
rs27663253 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Nsmaf | Mm_Celera | 4:6420230 | ATCCGGATACACTAC[A/G]TTCCCCATTCCTGCC | 18201 |
rs27663254 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Nsmaf | Mm_Celera | 4:6420229 | GATCCGGATACACTA[C/T]GTTCCCCATTCCTGC | 18201 |
rs27663255 | snp | A/G/T | 0.244898 | 0.249948 | intron-variant | Nsmaf | GRCm38.p3 | 4:6420166 | AGAATAAACAGCTCC[A/G/T]TGTTGACTCTGAGAC | 18201 |
rs27663256 | snp | A/T | 0.165289 | 0.235211 | intron-variant | Nsmaf | Mm_Celera | 4:6419822 | GCATACTGTACATAT[A/T]TAATCAGAAAGTTTT | 18201 |
rs27663257 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Nsmaf | Mm_Celera | 4:6419169 | TGCGCAGGACAGGAG[A/G]AAAATCTACATTTAA | 18201 |
rs27663258 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Nsmaf | Mm_Celera | 4:6419126 | AAAGCATTATTTCAA[A/G]ATAGTATGGGAAAAA | 18201 |
rs27663259 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Nsmaf | Mm_Celera | 4:6419067 | AGAGAATAATAGTTA[A/G]AGTAAATTAGGGCAT | 18201 |
rs27663260 | snp | A/G | 0.18 | 0.24 | intron-variant | Nsmaf | Mm_Celera | 4:6418919 | ATGGTGAGACACAAA[A/G]GGATTTTGTTCACTT | 18201 |
rs27663261 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Nsmaf | Mm_Celera | 4:6418833 | CACATGCACACTGCC[A/G]TGGAAGGTGCACATC | 18201 |
rs27663262 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Nsmaf | Mm_Celera | 4:6418571 | CCCGAGCTATGGAGA[C/T]GGCAGCAGCTGCAGG | 18201 |