SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs3720571 | snp | A/G | 0.415225 | 0.187619 | intron-variant | Senp7 | Mm_Celera | 16:56186837 | GCTTAGTGAAGTGGT[A/G]CAGATAAAATACAAA | 66315 |
rs3721136 | snp | A/G | 0.484429 | 0.0868505 | intron-variant | Senp7 | GRCm38.p3 | 16:56186905 | TAAGTCTCTCAGAGC[A/G]CCATAGCTGAGGAAA | 66315 |
rs4188243 | snp | C/T | 0.444444 | 0.157135 | upstream-variant-2KB | Senp7 | GRCm38.p3 | 16:56071989 | CTCCCTCCCTCCCTC[C/T]CTCTCTCTCTCTCTC | 66315 |
rs4188244 | snp | C/T | 0.444444 | 0.157135 | upstream-variant-2KB | Senp7 | GRCm38.p3 | 16:56072024 | TCTCTCTCTCTCTCT[C/T]TCTCTCTCTCTCTGC | 66315 |
rs4188245 | snp | C/T | 0.48 | 0.0979796 | upstream-variant-2KB, intron-variant | Senp7 | GRCm38.p3 | 16:56074234 | CCCCATCTCTCCCCA[C/T]GTCCTCATGGTGCTC | 66315 |
rs4188246 | snp | A/T | 0.493827 | 0.0552116 | upstream-variant-2KB, utr-variant-5-prime, intron-variant | Senp7 | Mm_Celera | 16:56075333 | GATAGGCTCGCAGGC[A/T]AAACAAGGCCCAGGA | 66315 |
rs4188247 | snp | C/T | 0.375 | 0.216506 | intron-variant | Senp7 | GRCm38.p3 | 16:56085048 | AGGGCTTTGAAAATG[C/T]TGAGGATATACTTTG | 66315 |
rs4188248 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Senp7 | Mm_Celera | 16:56085421 | TCTTCAACCTGAAAG[A/G]ATGTGTGTGTGTGTG | 66315 |
rs4188249 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Senp7 | Mm_Celera | 16:56085915 | CACACACACACACAC[A/G]CACACACACACACAC | 66315 |
rs4188250 | snp | G/T | 0.375 | 0.216506 | intron-variant | Senp7 | GRCm38.p3 | 16:56100373 | CACCCAAGGTACACT[G/T]AGATGCTTAATGGTT | 66315 |
rs4188251 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Senp7 | GRCm38.p3 | 16:56102226 | TTAAATCTTAAAAAA[A/G]AGGAAAAAGTTAAAA | 66315 |
rs4188253 | snp | C/T | 0.375 | 0.216506 | intron-variant | Senp7 | Mm_Celera | 16:56105866 | agggactagacaagg[C/T]tgcccactttctccc | 66315 |
rs4188254 | snp | C/T | 0.375 | 0.216506 | intron-variant | Senp7 | Mm_Celera | 16:56134982 | TTGTGTGTGTGTGTG[C/T]GCGCGCGCGCGCGCC | 66315 |
rs4188255 | snp | A/C | 0.48 | 0.0979796 | intron-variant, utr-variant-3-prime | Senp7 | GRCm38.p3 | 16:56141266 | ATATTTTCTAGATCC[A/C]TCCATTTGCCTGTGA | 66315 |
rs4188256 | snp | A/T | 0.499055 | 0.0217186 | intron-variant, downstream-variant-500B | Senp7 | GRCm38.p3 | 16:56142290 | TGTTTTATAGAGGCA[A/T]GCTTCCACACAACCA | 66315 |
rs4188257 | snp | A/T | 0.375 | 0.216506 | intron-variant | Senp7 | GRCm38.p3 | 16:56146274 | TTGCTCTAAGGAGAC[A/T]CCATGACCAAGGCAA | 66315 |
rs4188258 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Senp7 | Mm_Celera | 16:56148535 | GAGAGAGTTGTTGAG[A/G]AAAGACAGTTTGGCT | 66315 |
rs4188259 | snp | A/T | 0.453686 | 0.144955 | intron-variant | Senp7 | Mm_Celera | 16:56157146 | CCTAAATTTTGATCT[A/T]GAAAATCAAAGCACT | 66315 |
rs4188260 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Senp7 | Mm_Celera | 16:56165635 | GGTGTGTTCTTCCCC[G/T]GGGAAGACTATTGCT | 66315 |
rs4188261 | snp | C/T | 0.277778 | 0.248452 | missense | Senp7 | Mm_Celera | 16:56165871 | ACAGTGGACACCGCA[C/T]GTTTAAAGAGGTTCG | 66315 |
rs4188262 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Senp7 | Mm_Celera | 16:56167701 | TGTGTCTATATGCCT[A/G]TTTGTGCAGGTGTCC | 66315 |
rs4188263 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Senp7 | Mm_Celera | 16:56167913 | ATCTATATATGTATA[C/T]ATTACATATATAATA | 66315 |
rs4188264 | snp | C/T | 0.375 | 0.216506 | intron-variant | Senp7 | Mm_Celera | 16:56168300 | TTACTGGAGAGTTCT[C/T]TGATTTTTTTTTTTT | 66315 |
rs4188265 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Senp7 | Mm_Celera | 16:56168602 | ATTCCTGCCTGATTT[C/T]TTCAATGACCCAGTG | 66315 |
rs4188266 | snp | C/T | 0.375 | 0.216506 | intron-variant | Senp7 | Mm_Celera | 16:56170394 | AAAATGACAGTAGTA[C/T]TCTGTAGTGAAGAGT | 66315 |
rs4188267 | snp | C/T | 0.42 | 0.183303 | intron-variant | Senp7 | Mm_Celera | 16:56170933 | GGACAGCCAGGGCTA[C/T]ACAGAGAAACCCTGT | 66315 |
rs4188269 | snp | A/G | 0.498615 | 0.0262793 | intron-variant | Senp7 | GRCm38.p3 | 16:56178567 | CACCTCCTCCACTAG[A/G]CTTTAACATGTACCG | 66315 |
rs4188270 | snp | C/T | 0.5 | 0 | intron-variant | Senp7 | GRCm38.p3 | 16:56178715 | AGTCTACAAAGCCTG[C/T]CGCAGTGTACTGCCT | 66315 |
rs4188271 | snp | A/T | 0.375 | 0.216506 | intron-variant | Senp7 | GRCm38.p3 | 16:56180019 | TTTCTTTGAAAAAAA[A/T]TTTTTAAGAATCAGG | 66315 |
rs4188272 | snp | A/T | 0.499055 | 0.0217186 | intron-variant | Senp7 | GRCm38.p3 | 16:56180310 | AAATGGACCCAGCCA[A/T]TTTGTATTTCAGGTT | 66315 |
rs4188273 | snp | C/G | 0.375 | 0.216506 | intron-variant | Senp7 | Mm_Celera | 16:56181260 | CTCTGAACCTGTAAG[C/G]TAGCCCCAGTTAAAC | 66315 |
rs4188274 | snp | G/T | 0.408163 | 0.193609 | intron-variant | Senp7 | Mm_Celera | 16:56183596 | AGAAGTGTGTCACTG[G/T]GGGGGTGGGATTTGA | 66315 |
rs4188275 | snp | A/G | 0.375 | 0.216506 | intron-variant | Senp7 | Mm_Celera | 16:56185210 | GTCAGAGATCTGCTT[A/G]TTTCTGCCTCCTGAG | 66315 |
rs4188276 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Senp7 | Mm_Celera | 16:56185568 | AGGAGAGAGGAGAGA[A/G]AGAGAGATGTTTGGG | 66315 |
rs4188277 | snp | G/T | 0.498866 | 0.0237825 | intron-variant | Senp7 | GRCm38.p3 | 16:56185819 | CATAATATAAATAAC[G/T]TTGTTTCCTGAACTG | 66315 |
rs4188278 | snp | A/G | 0.489796 | 0.070696 | synonymous-codon | Senp7 | GRCm38.p3 | 16:56186095 | GGTGAAACGAAAAAC[A/G]CACCGTGAATTCAGT | 66315 |
rs4188279 | snp | A/G | 0.476371 | 0.106096 | intron-variant | Senp7 | GRCm38.p3 | 16:56186321 | ATGGCGAGATGGAGA[A/G]AAGACATGGAGACCA | 66315 |
rs4188280 | snp | G/T | 0.491493 | 0.0646602 | intron-variant | Senp7 | GRCm38.p3 | 16:56186453 | ACAGAAGATATCAAA[G/T]GAACATTTTAAAGGT | 66315 |
rs4188281 | snp | C/T | 0.396694 | 0.202437 | intron-variant | Senp7 | Mm_Celera | 16:56187352 | TTTGTTATTTAATTC[C/T]ATTTAAGGTCGTCTC | 66315 |
rs4188282 | snp | C/T | 0.385633 | 0.210009 | intron-variant | Senp7 | Mm_Celera | 16:56187491 | AGAACTACTGGATTT[C/T]CATAATGAAAGCAAT | 66315 |
rs4188283 | snp | A/G | 0.476371 | 0.106096 | utr-variant-3-prime | Senp7 | GRCm38.p3 | 16:56188412 | CTCCCTAAGTTTCCT[A/G]GAAAGCCGCTTACCA | 66315 |
rs6162828 | snp | C/T | 0.5 | 0 | intron-variant | Senp7 | GRCm38.p3 | 16:56162230 | ggctatacagagaaa[C/T]cctgtctcgaaaaac | 66315 |
rs6163348 | snp | A/G | 0.359862 | 0.224567 | intron-variant | Senp7 | Mm_Celera | 16:56162339 | AGAAATGCATTTGGA[A/G]TAGTAACTCATATTT | 66315 |
rs6173876 | snp | C/T | 0.5 | 0 | intron-variant | Senp7 | Mm_Celera | 16:56174686 | tatctatctatctat[C/T]tatctGCCTGTGTAA | 66315 |
rs6177089 | snp | A/C | 0.5 | 0 | intron-variant | Senp7 | Mm_Celera | 16:56162506 | CACAAATTTTCCATC[A/C]ATTTTTANTATAGAA | 66315 |
rs6177110 | snp | C/G | 0.5 | 0 | intron-variant | Senp7 | GRCm38.p3 | 16:56162514 | TTCCATCNATTTTTA[C/G]TATAGAAAATAAGTN | 66315 |
rs6177139 | snp | A/C/G | 0.255102 | 0.274943 | intron-variant | Senp7 | GRCm38.p3 | 16:56162529 | NTATAGAAAATAAGT[A/C/G]AAGTNTAGACCATTT | 66315 |
rs6177142 | snp | A/G | 0.5 | 0 | intron-variant | Senp7 | GRCm38.p3 | 16:56162534 | GAAAATAAGTNAAGT[A/G]TAGACCATTTAATAA | 66315 |
rs6177604 | snp | A/T | 0.359862 | 0.224567 | intron-variant | Senp7 | GRCm38.p3 | 16:56162606 | AAAATGTTTTATAGT[A/T]CCGAAAGAATATATT | 66315 |
rs6228285 | snp | C/T | 0.5 | 0 | intron-variant | Senp7 | Mm_Celera | 16:56171286 | ACATATGTACAGACA[C/T]ATACTCTGAGGCTCT | 66315 |
rs6288153 | snp | C/T | 0.5 | 0 | upstream-variant-2KB | Senp7, LOC105246121 | Mm_Celera | 16:56070877 | gttggggccggcctg[C/T]ggctctcatgtcccg | 66315 |
rs6288760 | snp | A/G | 0.5 | 0 | upstream-variant-2KB | Senp7, LOC105246121 | Mm_Celera | 16:56071031 | taaaggagaggggag[A/G]cccattccngctaaa | 66315 |
rs6288773 | snp | C/T | 0.5 | 0 | upstream-variant-2KB | Senp7, LOC105246121 | Mm_Celera | 16:56071040 | ggggagncccattcc[C/T]gctaaactggaggtg | 66315 |
rs6302155 | snp | A/T | 0.5 | 0 | upstream-variant-2KB | Senp7, LOC105246121 | Mm_Celera | 16:56071060 | aactggaggtgacca[A/T]gtgtaggatcagatg | 66315 |
rs6388703 | snp | C/T | 0.359862 | 0.224567 | intron-variant | Senp7 | Mm_Celera | 16:56160166 | TTGAGTGTAGCAGTA[C/T]ATACACTTTCTTTTA | 66315 |
rs6388742 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Senp7 | Mm_Celera | 16:56160190 | TCTTTTAAAATTCAG[A/G]TTAACACTNGTGGTA | 66315 |
rs6388757 | snp | G/T | 0.5 | 0 | intron-variant | Senp7 | Mm_Celera | 16:56160199 | ATTCAGNTTAACACT[G/T]GTGGTAGTAAGAAAA | 66315 |
rs6402354 | snp | A/G | 0.415225 | 0.187619 | intron-variant | Senp7 | GRCm38.p3 | 16:56160323 | AGATGGAAAGTTTCC[A/G]GGACAGGCTTTGCTT | 66315 |
rs6402456 | snp | A/G | 0.359862 | 0.224567 | intron-variant | Senp7 | GRCm38.p3 | 16:56160369 | ATCCCGACATAGCTG[A/G]GAGTAGACCCTACNC | 66315 |
rs6402480 | snp | A/G | 0.415225 | 0.187619 | intron-variant | Senp7 | GRCm38.p3 | 16:56160383 | GNGAGTAGACCCTAC[A/G]CACGCTGTTATAGTA | 66315 |
rs13471805 | snp | A/G | 0.391111 | 0.206368 | utr-variant-3-prime | Senp7 | GRCm38.p3 | 16:56188647 | GGAATGTTTTCCTAA[A/G]TAATAAGCCTATGTG | 66315 |
rs45643982 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Senp7 | Mm_Celera | 16:56162966 | AAGAAATATGTGGGC[A/G]CATAACATCAGATAT | 66315 |
rs45645154 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Senp7 | Mm_Celera | 16:56160307 | CTAGTCTTCTGCAAA[G/T]AGATGGAAAGTTTCC | 66315 |
rs45667546 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Senp7 | GRCm38.p3 | 16:56187602 | GTTCCACGGCAGCCC[A/G]TTTGTTCTTCTATCC | 66315 |
rs45688419 | snp | A/T | 0.391111 | 0.206368 | intron-variant | Senp7 | GRCm38.p3 | 16:56179651 | TTAATGCACCATTTT[A/T]AATAATAATCCTGGT | 66315 |
rs45688618 | snp | C/G | 0.391111 | 0.206368 | intron-variant | Senp7 | GRCm38.p3 | 16:56095866 | CTCATCAGATTCAAG[C/G]ACAACATACATCTTC | 66315 |
rs45727900 | snp | A/T | 0.32 | 0.24 | intron-variant | Senp7 | GRCm38.p3 | 16:56125122 | CCACGCAGGCCCACA[A/T]AGGAACTCCAGACTA | 66315 |
rs45738603 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Senp7 | Mm_Celera | 16:56161121 | TTGTGTTTGCAAGTT[C/T]TATCTCTGATGTAGT | 66315 |
rs45745642 | snp | G/T | 0.32 | 0.24 | intron-variant | Senp7 | GRCm38.p3 | 16:56186021 | TGCTGACTGATGAAG[G/T]TTTCTGCTCAAGCCA | 66315 |
rs45758248 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Senp7 | GRCm38.p3 | 16:56172397 | AGTTACATAGAAACT[A/G]TCAAATTACATTTAA | 66315 |
rs45786082 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Senp7 | Mm_Celera | 16:56138196 | TAATTATTTTGCCAG[A/C]ATCTTACATTTTAAA | 66315 |
rs45805225 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Senp7 | GRCm38.p3 | 16:56161359 | GATCTCAGTCACAAG[A/G]GAGTTCTGAGAAGTG | 66315 |
rs45844072 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Senp7 | GRCm38.p3 | 16:56160764 | CATTAAATTAGATTG[C/T]CTTAATTAGATACGG | 66315 |
rs45865881 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Senp7 | GRCm38.p3 | 16:56125202 | GACAGACACTCTGAC[G/T]TCTTCCCACTTTTGT | 66315 |
rs45868748 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Senp7 | GRCm38.p3 | 16:56179700 | AACAATATGAAGCTA[A/G]CAGTCTACCCATTTA | 66315 |
rs45881570 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Senp7 | Mm_Celera | 16:56171639 | TGTTACTTTTTGATA[C/T]ACATTTATTTTAGTT | 66315 |
rs45887768 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Senp7 | Mm_Celera | 16:56089626 | CTTGGAGATTAGGAT[C/T]TTGGGTCTTCAGTTT | 66315 |
rs45891678 | snp | G/T | 0.32 | 0.24 | intron-variant | Senp7 | GRCm38.p3 | 16:56120278 | CAGATTCTTCTGGTG[G/T]TGAGTGGCCACAGCC | 66315 |
rs45907782 | snp | A/G | 0.391111 | 0.206368 | utr-variant-3-prime | Senp7 | GRCm38.p3 | 16:56188976 | TTTCCTTCTCCACTT[A/G]TTTCAATGTCATATA | 66315 |
rs45924428 | snp | C/T | 0.391111 | 0.206368 | synonymous-codon | Senp7 | GRCm38.p3 | 16:56158500 | TCCATACAATCCTGA[C/T]GTAGAAAACATTTCC | 66315 |
rs45944444 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Senp7 | Mm_Celera | 16:56157798 | TCTCTGTGATATTTC[C/T]GATACAGTGAAAATT | 66315 |
rs45957478 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Senp7 | GRCm38.p3 | 16:56167495 | TGTTTGCACTTGTAC[C/T]TCATTTCCCATTTTT | 66315 |
rs45982558 | snp | C/T | 0.391111 | 0.206368 | intron-variant, utr-variant-3-prime | Senp7 | Mm_Celera | 16:56139710 | AACTTTCAAAAGATT[C/T]TTACCTAAGCCAATT | 66315 |
rs45987613 | snp | A/T | 0.165289 | 0.235211 | intron-variant | Senp7 | Mm_Celera | 16:56077848 | AAATGGCCTTTCTGC[A/T]GAGGATGTGTTATCA | 66315 |
rs45989094 | snp | C/T | 0.391111 | 0.206368 | synonymous-codon | Senp7 | GRCm38.p3 | 16:56165942 | CCACGCTATCCTTTT[C/T]CTCTGGCTTTCCTCA | 66315 |
rs46005128 | snp | A/T | 0.391111 | 0.206368 | intron-variant | Senp7 | GRCm38.p3 | 16:56148785 | GGTGAGAGGATGGAA[A/T]GTATTGGATGATAAA | 66315 |
rs46017870 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Senp7 | Mm_Celera | 16:56161088 | CAGAACTCATTTGCT[A/G]TCTATTTCAATTTTA | 66315 |
rs46034035 | snp | C/T | 0.32 | 0.24 | intron-variant | Senp7 | GRCm38.p3 | 16:56101644 | GGGTATCTCTTTCAA[C/T]TTTATTTGGGGGATC | 66315 |
rs46053888 | snp | C/T | 0.32 | 0.24 | intron-variant | Senp7 | GRCm38.p3 | 16:56125336 | CTGCTGATAAGGTGC[C/T]AGAAAGTTTCTATGC | 66315 |
rs46056442 | snp | C/T | 0.426035 | 0.177515 | intron-variant | Senp7 | Mm_Celera | 16:56163118 | ATCACCATTTAAGTA[C/T]TGAGAATACAACAAT | 66315 |
rs46076091 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Senp7 | Mm_Celera | 16:56156841 | AGAGATGAAAAGATC[G/T]GAAATATTTAAAAAC | 66315 |
rs46102773 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Senp7 | GRCm38.p3 | 16:56178542 | AAAATTAAAGACAGA[A/G]CCCTCATTTCACCTC | 66315 |
rs46109614 | snp | A/C | | | intron-variant | Senp7 | GRCm38.p3 | 16:56079478 | AGTTGTTCTTTAGTG[A/C]CTGGATCCTAAGGGC | 66315 |
rs46112632 | snp | G/T | 0.152778 | 0.230321 | intron-variant | Senp7 | GRCm38.p3 | 16:56167679 | CATGCACGTGTGCCT[G/T]CACCTGTGTGTCTAT | 66315 |
rs46121333 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Senp7 | GRCm38.p3 | 16:56171940 | GCTGCTTTCAAGTAG[C/T]TTCCCTGGTGGGAAG | 66315 |
rs46148309 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Senp7 | GRCm38.p3 | 16:56148770 | CAGTTAGAAAAGTAT[A/G]GTGAGAGGATGGAAA | 66315 |
rs46152571 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Senp7 | Mm_Celera | 16:56158020 | GTAAAACAGAATAAA[C/T]CTGGCAGCAGTCCTC | 66315 |
rs46175081 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Senp7 | Mm_Celera | 16:56082537 | AATTCTGTGTTCTGA[C/T]TAACTGAGGTTGGAA | 66315 |
rs46181899 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Senp7 | Mm_Celera | 16:56125698 | TCTGTAATAGGAACA[C/T]CTGAAATAATGTTTG | 66315 |
rs46183680 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Senp7 | GRCm38.p3 | 16:56093610 | TCACAGCGATGTAAG[A/G]TTTATTGCTACGCTC | 66315 |