SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs3700978 | snp | A/G | 0.5 | 0 | intron-variant | Zbtb20 | Mm_Celera | 16:43543103 | AATTATGTCTTTTTG[A/G]AAGAGGATGCTAGGA | 56490 |
rs4179132 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Zbtb20, Gm19522 | Mm_Celera | 16:42909162 | ACTCCACAACACACT[C/T]TCAAGGTTCAAGCCT | 56490 |
rs4179133 | snp | A/G | 0.333267 | 0.235726 | intron-variant | Zbtb20 | Mm_Celera | 16:42928326 | ATAATTTCTTCAAAG[A/G]ATCGTGGGTCCGTTC | 56490 |
rs4179134 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Zbtb20 | Mm_Celera | 16:42941360 | AGAAAATATCTAATT[A/T]AAAAAAAAAAAAAAA | 56490 |
rs4179135 | snp | C/T | 0.5 | 0 | intron-variant | Zbtb20 | Mm_Celera | 16:42943066 | tttctttctttcttt[C/T]tctttctttctttct | 56490 |
rs4179136 | snp | G/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | Zbtb20, BC002163 | Mm_Celera | 16:42953964 | TCTTGTGTGTGTGTG[G/T]GGGGGGGTTCTGATT | 56490 |
rs4179137 | snp | C/T | 0.375 | 0.216506 | intron-variant | Zbtb20 | Mm_Celera | 16:42957435 | CCTTGGAACCTCCCC[C/T]TGGGATAGATCCCAA | 56490 |
rs4179138 | snp | A/G | 0.375 | 0.216506 | intron-variant | Zbtb20 | Mm_Celera | 16:43008883 | CCCACCCACCCACTC[A/G]TACCTCTTGGCCATG | 56490 |
rs4179139 | snp | A/C | 0.5 | 0 | intron-variant | Zbtb20 | GRCm38.p3 | 16:43060825 | tctctctctctctct[A/C]tctctatatatatat | 56490 |
rs4179140 | snp | A/C | 0.48 | 0.0979796 | intron-variant | Zbtb20 | Mm_Celera | 16:43060827 | TCTCTCTCTCTCTCT[A/C]TCTATATATATATAT | 56490 |
rs4179141 | snp | A/G | 0.371124 | 0.218698 | intron-variant | Zbtb20 | GRCm38.p3 | 16:43067071 | AAAGAGTTTTCTATT[A/G]TGTATTTGAATTTTA | 56490 |
rs4179142 | snp | A/G | 0.489796 | 0.070696 | intron-variant | Zbtb20 | Mm_Celera | 16:43132011 | AATACGGGCTACACT[A/G]TGGAGTAATCATTCA | 56490 |
rs4179143 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Zbtb20 | GRCm38.p3 | 16:43216085 | GGTCACAAGCAGTTG[C/T]AGGTGCAGGGCACCA | 56490 |
rs4179144 | snp | A/G | 0.498866 | 0.0237825 | intron-variant | Zbtb20 | GRCm38.p3 | 16:43226883 | CTTATTTCCCTACTC[A/G]TTGATTCTAATTCCA | 56490 |
rs4179145 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Zbtb20 | GRCm38.p3 | 16:43238775 | GTTATACCCTCCACA[A/G]CATCTGCAAAATAAA | 56490 |
rs4179146 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Zbtb20 | GRCm38.p3 | 16:43240560 | GTTCTAACTATGAAT[A/G]CAGCAGTCTCCTGAG | 56490 |
rs4179147 | snp | G/T | 0.5 | 0 | intron-variant | Zbtb20 | Mm_Celera | 16:43288845 | AATACAAAGTAAATA[G/T]CATTATGACACATAT | 56490 |
rs4179148 | snp | A/G | 0.489796 | 0.070696 | intron-variant | Zbtb20 | Mm_Celera | 16:43300171 | AGTAATGTTTCAAGT[A/G]CCTTAGCCAGTGACT | 56490 |
rs4179149 | snp | A/G | 0.375 | 0.216506 | intron-variant | Zbtb20 | Mm_Celera | 16:43310620 | GTTTAATGTCTCAGG[A/G]TGGAAAATGCTGGTG | 56490 |
rs4179150 | snp | G/T | 0.375 | 0.216506 | intron-variant | Zbtb20 | Mm_Celera | 16:43344139 | TTCTGTGTGTGGGGG[G/T]TTTTTTTTTTCATTT | 56490 |
rs4179151 | snp | A/G | 0.32 | 0.24 | intron-variant | Zbtb20 | Mm_Celera | 16:43354184 | CGAACTCAGAAATCT[A/G]CCTGCCTCTGCCTCC | 56490 |
rs4179152 | snp | C/G/T | 0.4928 | 0.0595664 | intron-variant | Zbtb20 | GRCm38.p3 | 16:43354341 | TAATTAATTGAGCGA[C/G/T]TTGTTTTCAGAAGCA | 56490 |
rs4179153 | snp | A/G | 0.5 | 0 | intron-variant | Zbtb20 | Mm_Celera | 16:43406735 | CAGGCAGATCTCTAA[A/G]TTTGAGGACAGCCTG | 56490 |
rs4179154 | snp | C/T | 0.453686 | 0.144955 | intron-variant | Zbtb20 | GRCm38.p3 | 16:43408295 | CAAGTCAGGGTGGAA[C/T]TTAAGAGGTGATGTG | 56490 |
rs4179155 | snp | A/G | 0.226843 | 0.248925 | intron-variant, downstream-variant-500B | Zbtb20, Gm15713 | Mm_Celera | 16:43410488 | GGAAGGAGAATGTGG[A/G]CCAAAAGATTGCGAC | 56490 |
rs4179156 | snp | C/T | 0.487535 | 0.077957 | intron-variant | Zbtb20 | GRCm38.p3 | 16:43425116 | AATGTGTACTCATTC[C/T]TCTGAATTTATATTG | 56490 |
rs4179157 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Zbtb20 | Mm_Celera | 16:43426351 | CCCATCTATCTGATG[G/T]AGGAATTCCTCACTT | 56490 |
rs4179158 | snp | C/T | 0.489796 | 0.070696 | intron-variant | Zbtb20 | Mm_Celera | 16:43426569 | ACATTGGTCCAGTTG[C/T]CCCTCTGTTTTCAAA | 56490 |
rs4179159 | snp | A/C | 0.408163 | 0.193609 | intron-variant | Zbtb20 | Mm_Celera | 16:43434439 | ATCAGGATAATATAA[A/C]CAACAACAACAAAAA | 56490 |
rs4179160 | snp | A/C | 0.408163 | 0.193609 | intron-variant | Zbtb20 | Mm_Celera | 16:43434442 | AGGATAATATAAACA[A/C]CAACAACAAAAAAAG | 56490 |
rs4179161 | snp | A/C | 0.408163 | 0.193609 | intron-variant | Zbtb20 | Mm_Celera | 16:43434445 | ATAATATAAACAACA[A/C]CAACAAAAAAAGTTC | 56490 |
rs4179162 | snp | A/G | 0.483471 | 0.0893938 | intron-variant | Zbtb20 | Mm_Celera | 16:43442253 | AAGCATTTAAAATGG[A/G]AAGAAATGAATGTTC | 56490 |
rs4179163 | snp | C/G | 0.483471 | 0.0893938 | intron-variant | Zbtb20 | Mm_Celera | 16:43447366 | CCAGTGAACACCTTA[C/G]CAAAGGGTAGGGCAG | 56490 |
rs4179164 | snp | C/G | 0.455 | 0.143091 | intron-variant | Zbtb20 | GRCm38.p3 | 16:43452956 | ATGTTCCTTCCTTTT[C/G]CCATGACAAAAACCA | 56490 |
rs4179165 | snp | A/T | 0.367755 | 0.220531 | intron-variant | Zbtb20 | GRCm38.p3 | 16:43481494 | ATGGTGCGCTGGACT[A/T]TGTTTCTGTTTGTTT | 56490 |
rs4179166 | snp | C/G | 0.5 | 0 | intron-variant | Zbtb20 | Mm_Celera | 16:43482338 | CTGAGTAGCAGGCTG[C/G]CAAATTCCCTGCCTT | 56490 |
rs4179168 | snp | C/G | 0.5 | 0 | intron-variant | Zbtb20 | Mm_Celera | 16:43483775 | TACATATATATGTCT[C/G]TGTGTGTGTGTGTGT | 56490 |
rs4179169 | snp | C/T | 0.5 | 0 | intron-variant | Zbtb20 | GRCm38.p3 | 16:43487602 | GGTCCCTGTTGAGTT[C/T]CTTAGACTCAACCAC | 56490 |
rs4179170 | snp | A/G | 0.5 | 0 | intron-variant | Zbtb20 | GRCm38.p3 | 16:43489479 | TGGCATGCTAGAACC[A/G]AGCCCAGGGAAACAT | 56490 |
rs4179171 | snp | A/G | 0.455 | 0.143091 | intron-variant | Zbtb20 | Mm_Celera | 16:43493377 | CTTACTGTCCGGTCA[A/G]GATTCATTATTTTTT | 56490 |
rs4179172 | snp | A/G | 0.487535 | 0.077957 | intron-variant | Zbtb20 | Mm_Celera | 16:43493992 | TTGCATTAATTTTAA[A/G]GATGTGCAAATGCAT | 56490 |
rs4179173 | snp | A/G | 0.487535 | 0.077957 | intron-variant | Zbtb20 | GRCm38.p3 | 16:43496195 | CCAGTCATCATTGCA[A/G]CTTGAAACTCCCTAA | 56490 |
rs4179174 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Zbtb20 | GRCm38.p3 | 16:43497152 | CCAGAGCCAACAAGG[C/T]CAGGTCAGAGTGTCC | 56490 |
rs4179175 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Zbtb20 | GRCm38.p3 | 16:43497497 | ACGTGACTAATAAAG[G/T]CTCTTGTAACATAAG | 56490 |
rs4179176 | snp | A/T | 0.48 | 0.0979796 | intron-variant | Zbtb20 | Mm_Celera | 16:43498181 | CTCTCTCATTCTCTC[A/T]CTCTCTCTCTCTCTC | 56490 |
rs4179178 | snp | C/T | 0.5 | 0 | intron-variant | Zbtb20 | Mm_Celera | 16:43499883 | ATATATATATATACA[C/T]ACACACACACACATA | 56490 |
rs4179179 | snp | A/G | 0.444444 | 0.157135 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | Zbtb20 | GRCm38.p3 | 16:43508321 | TGCACACTGTACTTA[A/G]GGTAAGTACTATTCA | 56490 |
rs4179180 | snp | C/T | 0.496528 | 0.0415217 | intron-variant, upstream-variant-2KB | Zbtb20 | Mm_Celera | 16:43509390 | CAACCTACTACCTTT[C/T]ATTGCCAATCGGTAT | 56490 |
rs4179181 | snp | A/G | 0.489796 | 0.070696 | intron-variant, upstream-variant-2KB | Zbtb20 | Mm_Celera | 16:43509636 | TATGTTTATAAACAT[A/G]TATTTATATCCTTAT | 56490 |
rs4179182 | snp | G/T | 0.476371 | 0.106096 | intron-variant | Zbtb20 | GRCm38.p3 | 16:43513178 | GTGTAATCAAGGACA[G/T]AATTCAGCTCTTCCA | 56490 |
rs4179183 | snp | A/T | 0.495868 | 0.0452663 | intron-variant | Zbtb20 | GRCm38.p3 | 16:43517021 | TGAGGGTTTTTTTTT[A/T]AAACTGTATTTCCTA | 56490 |
rs4179184 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Zbtb20 | Mm_Celera | 16:43518527 | TCTGTAAGTAAACCC[A/G]ATTAGGCATATCCAC | 56490 |
rs4179185 | snp | C/G | 0.32 | 0.24 | intron-variant | Zbtb20 | Mm_Celera | 16:43519798 | AGTGAAAATGATCCT[C/G]TTTTGATTCCTCAGA | 56490 |
rs4179186 | snp | C/T | 0.483471 | 0.0893938 | intron-variant | Zbtb20 | Mm_Celera | 16:43520575 | GAAACATAAAGTTCA[C/T]ATGCCTGGCTCCTAA | 56490 |
rs4179187 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Zbtb20 | GRCm38.p3 | 16:43521613 | TCAGCCCCAGCATGG[C/T]TGCTGAGGGTCTCCT | 56490 |
rs4179188 | snp | A/T | 0.5 | 0 | intron-variant | Zbtb20 | Mm_Celera | 16:43522440 | AAATAATAAAAAAAA[A/T]TTTTTTTCTCATTAG | 56490 |
rs4179190 | snp | A/G | 0.5 | 0 | intron-variant | Zbtb20 | Mm_Celera | 16:43527098 | TTGTTTGTGTAGAGA[A/G]CAGGGCAACATCAGG | 56490 |
rs4179191 | snp | A/G | 0.491493 | 0.0646602 | intron-variant | Zbtb20 | Mm_Celera | 16:43530969 | TGACTTTGAAAATCT[A/G]TCTTAAAGGAACAAC | 56490 |
rs4179192 | snp | A/C/G | 0.444444 | 0.157135 | intron-variant | Zbtb20 | GRCm38.p3 | 16:43531223 | CCCTCTCTCCCAGCC[A/C/G]CTCCTCCCCCTCCAT | 56490 |
rs4179193 | snp | C/G | 0.235537 | 0.249581 | intron-variant | Zbtb20 | Mm_Celera | 16:43531488 | CTACAGTGCAGTCCT[C/G]CTCTTGCTTAATTAA | 56490 |
rs4179194 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Zbtb20 | GRCm38.p3 | 16:43533445 | CTCCTTCTACTGTGC[C/T]GTCCTGCCTCAGTCA | 56490 |
rs4179195 | snp | C/T | 0.46281 | 0.131194 | intron-variant | Zbtb20 | Mm_Celera | 16:43538464 | CAAAGAGACATCATT[C/T]TCCTGGTCAGGCATT | 56490 |
rs4179196 | snp | A/C | 0.48 | 0.0979796 | intron-variant | Zbtb20 | Mm_Celera | 16:43540871 | GAAAAAGTTTAGTTG[A/C]ACTTGGATTTTCTGT | 56490 |
rs4179197 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Zbtb20 | Mm_Celera | 16:43546329 | ACTGATGCAGTCAGG[C/T]AGCTCTGAGCCCGAT | 56490 |
rs4179198 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Zbtb20 | GRCm38.p3 | 16:43546343 | GCAGCTCTGAGCCCG[A/G]TACCCCTGTCTTCTC | 56490 |
rs4179199 | snp | A/T | 0.489796 | 0.070696 | intron-variant | Zbtb20 | GRCm38.p3 | 16:43546538 | AGTGTGGCTGAACAC[A/T]ATGGAGAGGGTACTG | 56490 |
rs4179200 | snp | C/G | 0.495868 | 0.0452663 | intron-variant | Zbtb20 | Mm_Celera | 16:43547545 | TGTGGGGACAGATGA[C/G]CCCTTAACCTGGGAA | 56490 |
rs4179201 | snp | A/G | 0.495 | 0.0497494 | intron-variant | Zbtb20 | GRCm38.p3 | 16:43558989 | GAATAGCGACATGCA[A/G]CTACTGTCAGATGCA | 56490 |
rs4179202 | snp | A/G | 0.495 | 0.0497494 | intron-variant | Zbtb20 | Mm_Celera | 16:43568650 | TCTGTGCTTTCTAAG[A/G]CTGTACTCCCTGGGG | 56490 |
rs4179203 | snp | G/T | 0.475309 | 0.108333 | intron-variant | Zbtb20 | GRCm38.p3 | 16:43569605 | GAAAACACTGTGAAA[G/T]AAACAAACAAAGCAT | 56490 |
rs4179204 | snp | A/G | 0.495868 | 0.0452663 | intron-variant | Zbtb20 | Mm_Celera | 16:43574781 | GTGCAATTTCTCCAG[A/G]GTTAGACCTCATGGG | 56490 |
rs4179205 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Zbtb20 | GRCm38.p3 | 16:43575671 | AGGCAGCCAATACAC[A/G]TGGCCCATGAGATAA | 56490 |
rs4179206 | snp | A/G | 0.375 | 0.216506 | intron-variant | Zbtb20 | GRCm38.p3 | 16:43578847 | GGAAAGGAAAGGAAA[A/G]GAAAGGAAAGGAAAG | 56490 |
rs4179207 | snp | C/G | 0.5 | 0 | intron-variant | Zbtb20 | GRCm38.p3 | 16:43579178 | AAGCAGGGACTTGTT[C/G]CCTGGAGCATCTTGG | 56490 |
rs4179208 | snp | C/T | 0.46281 | 0.131194 | intron-variant | Zbtb20 | GRCm38.p3 | 16:43580389 | ATTCCTGGCTATCCA[C/T]GGGCACCTTGGACAT | 56490 |
rs4179209 | snp | C/T | 0.489796 | 0.070696 | intron-variant | Zbtb20 | GRCm38.p3 | 16:43580903 | CTGAGTGGAGCCAAG[C/T]TCTCCCTTCAAGGAC | 56490 |
rs4179210 | snp | C/T | 0.4928 | 0.0595664 | intron-variant | Zbtb20 | Mm_Celera | 16:43582886 | CCTGTCATGCATTCC[C/T]TTTTGCTCAGTTTGG | 56490 |
rs4179211 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Zbtb20 | Mm_Celera | 16:43583211 | GTGCCAGAAAAATGA[A/G]AAACATTTTGGCCCC | 56490 |
rs4179212 | snp | C/T | 0.489796 | 0.070696 | intron-variant | Zbtb20 | Mm_Celera | 16:43588980 | GCAAGGTGAACCATT[C/T]CTGTTATTCAAATAA | 56490 |
rs4179213 | snp | C/G | 0.498866 | 0.0237825 | intron-variant | Zbtb20 | Mm_Celera | 16:43591718 | TTTTACAAGCAAAAA[C/G]CCTGGTAAGCAAAGC | 56490 |
rs4179214 | snp | A/G | 0.492188 | 0.0620098 | intron-variant | Zbtb20 | Mm_Celera | 16:43592397 | CCATGGAGCATAAAC[A/G]TCTTCATTTATAAAT | 56490 |
rs4179215 | snp | A/G | 0.5 | 0 | intron-variant | Zbtb20 | Mm_Celera | 16:43592410 | ACGTCTTCATTTATA[A/G]ATGAAATAACTGGTC | 56490 |
rs4179216 | snp | C/G | 0.5 | 0 | intron-variant | Zbtb20 | Mm_Celera | 16:43592574 | TATTATTTTTAATTA[C/G]TTTTCAGAAAAGTCA | 56490 |
rs4179217 | snp | A/G | 0.499055 | 0.0217186 | intron-variant | Zbtb20 | Mm_Celera | 16:43596056 | GCATGTTGATGTGGA[A/G]CTGAAAAGGAGAGCA | 56490 |
rs4179218 | snp | A/G | 0.5 | 0 | intron-variant | Zbtb20 | Mm_Celera | 16:43596786 | TGAGTGTGAGTGGAC[A/G]AGGTGGGGATAGTTC | 56490 |
rs4179219 | snp | G/T | 0.5 | 0 | intron-variant | Zbtb20 | GRCm38.p3 | 16:43596900 | GCTTCCTTGAGTTTG[G/T]ATTCCAGGCTTATAC | 56490 |
rs4179220 | snp | G/T | 0.5 | 0 | intron-variant | Zbtb20 | GRCm38.p3 | 16:43599124 | TGTGTAGACCTAACG[G/T]TCTGAGTTCTGTCCA | 56490 |
rs4179221 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Zbtb20 | Mm_Celera | 16:43599279 | AGACAGATGAATGGA[C/T]GGGCAGAAAGGCAGA | 56490 |
rs4179222 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Zbtb20 | GRCm38.p3 | 16:43600507 | CAGACAGAATCACAG[C/T]TCTGAGTCAGTTTCC | 56490 |
rs4179223 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Zbtb20 | Mm_Celera | 16:43601488 | ACATGTTAAGATCCC[G/T]TCTAAGGTAAAGGGT | 56490 |
rs4179224 | snp | C/T | 0.4608 | 0.1344 | intron-variant | Zbtb20 | GRCm38.p3 | 16:43602099 | CATGTTTTTATATAA[C/T]GGCAGACAAACGAGG | 56490 |
rs4179225 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Zbtb20 | GRCm38.p3 | 16:43602860 | TAGTAAGAAGAGAAT[A/G]GTGAGGATGGAAACC | 56490 |
rs4179226 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Zbtb20 | Mm_Celera | 16:43605113 | CATGAAGTTGTTTTT[A/G]TGCATGTGCATGCAT | 56490 |
rs4179229 | snp | A/C | 0.471655 | 0.115624 | intron-variant | Zbtb20 | Mm_Celera | 16:43606361 | ACTACAAAACAGAGA[A/C]CTAAGTTACAACTGA | 56490 |
rs4179230 | snp | A/G/T | 0.48 | 0.0979796 | intron-variant | Zbtb20 | GRCm38.p3 | 16:43608665 | CACTTGTGAGTTCCA[A/G/T]GACAGACTGAGTGGC | 56490 |
rs4179231 | snp | C/G | 0.471655 | 0.115624 | synonymous-codon | Zbtb20 | Mm_Celera | 16:43610063 | GACCACGCACTGCCG[C/G]AAGCAGCCCCGGCCT | 56490 |
rs4179232 | snp | C/T | 0.476371 | 0.106096 | synonymous-codon | Zbtb20 | GRCm38.p3 | 16:43610492 | CAGCTCCGATAAGGG[C/T]GTCCTACAGCAGCCT | 56490 |
rs4179233 | snp | C/T | 0.499567 | 0.0146995 | synonymous-codon | Zbtb20 | Mm_Celera | 16:43610765 | AGTGTCCCAGCCCGG[C/T]CTGTCCACCTTTACT | 56490 |
rs4179234 | snp | A/C | 0.5 | 0 | intron-variant | Zbtb20 | Mm_Celera | 16:43611399 | GATAGATAATAGATA[A/C]ATAGATGGTTATAGA | 56490 |
rs4179235 | snp | A/G | 0.495 | 0.0497494 | intron-variant | Zbtb20 | GRCm38.p3 | 16:43612927 | ACTTTGCTAATCTTG[A/G]ATCCATACATCCCTT | 56490 |