SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs4225169 | snp | C/T | 0.21875 | 0.248039 | downstream-variant-500B | Tnip2 | Mm_Celera | 5:34495801 | AATTCTGTGGCTATA[C/T]AGCACCTGGAAATCT | 231130 |
rs4225170 | snp | C/T | 0.21875 | 0.248039 | downstream-variant-500B | Tnip2 | Mm_Celera | 5:34495849 | TTCCCTACTCCTTTG[C/T]TACCTGCAGCATATG | 231130 |
rs4225171 | snp | C/G | 0.1128 | 0.208988 | downstream-variant-500B | Tnip2 | Mm_Celera | 5:34495875 | ATATGTAAGCACATT[C/G]TTGAACCAGCTCTAC | 231130 |
rs4225172 | snp | A/G | 0.375 | 0.216506 | downstream-variant-500B | Tnip2 | Mm_Celera | 5:34495879 | GTAAGCACATTGTTG[A/G]ACCAGCTCTACTCCA | 231130 |
rs4225173 | snp | A/C | 0.375 | 0.216506 | downstream-variant-500B | Tnip2 | Mm_Celera | 5:34495997 | attgaggCAAGACAG[A/C]AGGAATGTTTCTCCT | 231130 |
rs4225174 | snp | A/G | 0.21875 | 0.248039 | downstream-variant-500B | Tnip2 | Mm_Celera | 5:34495999 | tgaggCAAGACAGAA[A/G]GAATGTTTCTCCTTA | 231130 |
rs4225175 | snp | A/G | 0.21875 | 0.248039 | utr-variant-3-prime | Tnip2 | Mm_Celera | 5:34496104 | CACAGTAGTAAAGCC[A/G]TTTATTATAAAAATA | 231130 |
rs13470478 | snp | A/C | | | missense | Tnip2 | Mm_Celera | 5:34503644 | GATGAGACCCACCAA[A/C]TGCGCAGGACATTGG | 231130 |
rs33471614 | snp | A/G | 0.5 | 0 | utr-variant-3-prime | Tnip2 | GRCm38.p3 | 5:34496305 | TGGAGCTACCACCCT[A/G]GAAAGAGGACACACT | 231130 |
rs36246345 | snp | C/G | 0.375 | 0.216506 | missense | Tnip2 | GRCm38.p3 | 5:34496938 | TCCGACAGGGTCCTG[C/G]CTCCCGGGAGTCCTG | 231130 |
rs36269440 | snp | C/T | 0.297521 | 0.245442 | upstream-variant-2KB | Tnip2 | Mm_Celera | 5:34514942 | ACTAGAGAATGAGTG[C/T]GTATTTCTTTTCTAT | 231130 |
rs36274922 | snp | A/G | 0.18 | 0.24 | upstream-variant-2KB | Tnip2 | Mm_Celera | 5:34514734 | TGGTTGAGCCTGCAG[A/G]AACACACTCACTTGC | 231130 |
rs36354675 | snp | A/G | 0.375 | 0.216506 | intron-variant | Tnip2 | GRCm38.p3 | 5:34498255 | CTAAAGCCCTCTGGC[A/G]CCACTGCCTTGTCCT | 231130 |
rs36384402 | snp | C/T | 0.32 | 0.24 | missense | Tnip2 | Mm_Celera | 5:34513813 | GCTGTAGTTGCTGGC[C/T]GGCCTCGTGGTACAG | 231130 |
rs36442551 | snp | A/G | 0.46875 | 0.121031 | intron-variant | Tnip2 | Mm_Celera | 5:34507937 | AAAAATAAGTCTTGA[A/G]ATTCCTTTTCCATTG | 231130 |
rs36461375 | snp | A/C | 0.375 | 0.216506 | utr-variant-3-prime | Tnip2 | GRCm38.p3 | 5:34496217 | TCTGCTGAGTTTGGG[A/C]AGGTTCTAGTGTATC | 231130 |
rs36464482 | snp | A/G | 0.489796 | 0.070696 | intron-variant | Tnip2 | Mm_Celera | 5:34507865 | ATGGATTATGTTCAA[A/G]GACACATCTGGAGTC | 231130 |
rs36710723 | snp | A/G | 0.277778 | 0.248452 | upstream-variant-2KB | Tnip2 | GRCm38.p3 | 5:34515739 | aaaTCAACAACAAAA[A/G]GAGTCCTGTTTCCAG | 231130 |
rs36753472 | snp | C/T | 0.32 | 0.24 | upstream-variant-2KB | Tnip2 | GRCm38.p3 | 5:34514892 | AAAGATGGGTCACAG[C/T]TGCTTCCTTCCCTAC | 231130 |
rs36781086 | snp | A/G | 0.495868 | 0.0452663 | upstream-variant-2KB | Tnip2 | GRCm38.p3 | 5:34514685 | TCTGCTCAGTCTTCT[A/G]CTCTCAATACCCTGT | 231130 |
rs36925533 | snp | A/T | 0.444444 | 0.157135 | upstream-variant-2KB | Tnip2 | GRCm38.p3 | 5:34515566 | CATCCTCTAAAAAGG[A/T]CTACTCTTGGAAGGC | 231130 |
rs36970233 | snp | A/G | 0.375 | 0.216506 | intron-variant | Tnip2 | GRCm38.p3 | 5:34498014 | CCAAAAGCCCAGCAA[A/G]CCCACAGACATGTTA | 231130 |
rs37000121 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Tnip2 | Mm_Celera | 5:34513181 | CAGGACGTCAGGACT[C/T]GGTACTCCTCAAACA | 231130 |
rs37029160 | snp | C/G | 0.375 | 0.216506 | intron-variant | Tnip2 | GRCm38.p3 | 5:34502081 | TCTCTATACTTTGGG[C/G]AAGCTGCTGATACCT | 231130 |
rs37085540 | snp | C/T | 0.297521 | 0.245442 | intron-variant | Tnip2 | GRCm38.p3 | 5:34502871 | CACCACCCAAACTAT[C/T]CTGGCCTGGAGCCAC | 231130 |
rs37120823 | snp | C/T | 0.32 | 0.24 | upstream-variant-2KB | Tnip2 | Mm_Celera | 5:34514866 | CTTCCAGCCCAAAAC[C/T]TCTGCTCAGAAAAGA | 231130 |
rs37476974 | snp | A/C | 0.489796 | 0.070696 | intron-variant | Tnip2 | Mm_Celera | 5:34513366 | TTACCTGCGCCTCTG[A/C]TCCCCACGCCCTTCA | 231130 |
rs37524714 | snp | A/G | 0.152778 | 0.230321 | upstream-variant-2KB | Tnip2 | Mm_Celera | 5:34515773 | CTGTGCATATGGGCA[A/G]GCTCTGCACAACAGG | 231130 |
rs37584602 | snp | C/T | 0.375 | 0.216506 | intron-variant | Tnip2 | GRCm38.p3 | 5:34501740 | CCAGACATTCAACAC[C/T]ACAGAGGGACTGGTA | 231130 |
rs37709363 | snp | A/G | 0.396694 | 0.202437 | missense | Tnip2 | GRCm38.p3 | 5:34513678 | GCTGCTCACGGAAGC[A/G]CTCCACCTGATCCAG | 231130 |
rs37716918 | snp | A/G | 0.375 | 0.216506 | intron-variant | Tnip2 | GRCm38.p3 | 5:34499312 | AATCTGAGAAAAGAC[A/G]GAATATTCATGGCTA | 231130 |
rs37741016 | snp | C/T | 0.375 | 0.216506 | intron-variant | Tnip2 | Mm_Celera | 5:34513581 | CTCCAACAAGTTCCC[C/T]AGGCCGCCTTGCGCA | 231130 |
rs37826289 | snp | A/G | 0.426035 | 0.177515 | upstream-variant-2KB | Tnip2 | GRCm38.p3 | 5:34514374 | CTTCCGGGACTTGAC[A/G]TGCGTTTCTTCATAG | 231130 |
rs37897746 | snp | C/T | 0.375 | 0.216506 | intron-variant | Tnip2 | GRCm38.p3 | 5:34508565 | AAATTTAAATTTGTA[C/T]ACAATCTTGTTTAAT | 231130 |
rs37940468 | snp | A/T | 0.375 | 0.216506 | intron-variant | Tnip2 | GRCm38.p3 | 5:34501999 | CCTATATAGAAACAC[A/T]TACAACTGTGTTCCT | 231130 |
rs37955101 | snp | A/G | 0.132653 | 0.220748 | upstream-variant-2KB | Tnip2 | Mm_Celera | 5:34515844 | CAAAGTAACAAAGAC[A/G]TGATATTGCTTCAAG | 231130 |
rs38067175 | snp | A/T | 0.375 | 0.216506 | utr-variant-3-prime | Tnip2 | GRCm38.p3 | 5:34496419 | TGCAGCTTTGAATTG[A/T]CAGCTCACTCCAAAC | 231130 |
rs38277009 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Tnip2 | Mm_Celera | 5:34511866 | TCTAGCTGCAGTGGT[A/T]ATCTTGAAAACAAGC | 231130 |
rs38292009 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Tnip2 | Mm_Celera | 5:34513519 | CTCGAGCTTCATATC[C/T]TCGCGACCCTCAAGA | 231130 |
rs38574608 | snp | A/G | 0.489796 | 0.070696 | intron-variant | Tnip2 | GRCm38.p3 | 5:34510648 | TTCTGTTCTGGTTAT[A/G]GGGATCTCCTTTACC | 231130 |
rs38683405 | snp | C/G | 0.152778 | 0.230321 | upstream-variant-2KB | Tnip2 | Mm_Celera | 5:34515390 | CTCTTCACTACTATT[C/G]CTGTGTGTAGCCTAG | 231130 |
rs38893678 | snp | C/T | 0.375 | 0.216506 | intron-variant | Tnip2 | GRCm38.p3 | 5:34501349 | TTGTCATCAAGTCTA[C/T]AGGGATAAGTACATG | 231130 |
rs39042124 | snp | C/G | 0.375 | 0.216506 | upstream-variant-2KB | Tnip2 | Mm_Celera | 5:34514673 | TGTGTCTCCTTTTCT[C/G]CTCAGTCTTCTACTC | 231130 |
rs39513575 | snp | C/T | 0.277778 | 0.248452 | missense | Tnip2 | Mm_Celera | 5:34513849 | AGAGCGCTGCGGCCG[C/T]ACGCGGGGCCCCGTC | 231130 |
rs52177975 | snp | C/T | | | upstream-variant-2KB | Tnip2 | Mm_Celera | 5:34515941 | TGATATGTATATGAG[C/T]ATATATACTATACAT | 231130 |
rs52314705 | snp | C/T | | | upstream-variant-2KB | Tnip2 | Mm_Celera | 5:34515972 | GTATGTGTGAGTGTG[C/T]GATATGTGTGTGATA | 231130 |
rs211888808 | snp | A/C | | | intron-variant | Tnip2 | Mm_Celera | 5:34500595 | GGAGGCTGTCCATGG[A/C]CGCATGGGGGGTGGG | 231130 |
rs211924060 | snp | A/T | | | intron-variant | Tnip2 | Mm_Celera | 5:34500041 | TGGCCTCGTATTCAC[A/T]GGATCCACCTGCCTC | 231130 |
rs211997263 | snp | C/T | | | intron-variant | Tnip2 | Mm_Celera | 5:34508144 | CCACATGGTGACTTA[C/T]AACCATCTATAGGGG | 231130 |
rs212029962 | snp | C/G | | | upstream-variant-2KB | Tnip2 | Mm_Celera | 5:34514960 | ATTTCTTTTCTATTA[C/G]TGTGACAAAATGCCA | 231130 |
rs212032809 | snp | C/T | | | intron-variant | Tnip2 | Mm_Celera | 5:34508741 | TTGGAGACAGGGTTT[C/T]TCTGTGTAGCAGTTC | 231130 |
rs212330979 | snp | C/T | | | upstream-variant-2KB | Tnip2 | Mm_Celera | 5:34514529 | CAGAAGACAAGAGGG[C/T]GCCCACCCTTTCCTT | 231130 |
rs212346011 | in-del | -/TGTGTGTGTGTGTG | | | upstream-variant-2KB | Tnip2 | Mm_Celera | 5:34515888 | GAGTCTTTTTTAAAA[-/TGTGTGTGTGTGTG]TGTGTGTGTGTGTGT | 231130 |
rs212400758 | snp | C/T | | | intron-variant | Tnip2 | Mm_Celera | 5:34498732 | AAAGGCATGTATGTC[C/T]AGCTTTCCATGCCTC | 231130 |
rs212496091 | snp | C/T | | | intron-variant | Tnip2 | Mm_Celera | 5:34511056 | AAATGCTTTCTTTTT[C/T]CCCCCTCTAGAATTT | 231130 |
rs212662346 | snp | C/T | | | intron-variant | Tnip2 | Mm_Celera | 5:34505377 | GAAAACAGATATGCA[C/T]GTGGTGCCCAGACAT | 231130 |
rs212979350 | snp | A/G | | | intron-variant | Tnip2 | Mm_Celera | 5:34501674 | CAGTTGGCTGACCCA[A/G]AGGGAAAGCAGCATA | 231130 |
rs213020852 | snp | C/T | | | intron-variant | Tnip2 | Mm_Celera | 5:34509605 | TAGAAGTGTATACCA[C/T]CATACCATGAGAGCC | 231130 |
rs213300649 | in-del | -/GT | | | intron-variant | Tnip2 | Mm_Celera | 5:34508941 | ATGAATGAGAGAATA[-/GT]GTGTGTGTGTGTGTG | 231130 |
rs213330104 | snp | A/G | | | intron-variant | Tnip2 | Mm_Celera | 5:34498905 | GGCCAGACACTGACA[A/G]AACTGTCAGTAAAGC | 231130 |
rs213433195 | snp | C/T | | | intron-variant | Tnip2 | Mm_Celera | 5:34510134 | AAAAAGGCACGGGGG[C/T]TGGAGAGGTGGCTCA | 231130 |
rs213448370 | snp | C/G | | | intron-variant | Tnip2 | Mm_Celera | 5:34507512 | CTCTGCTTCTCCTGA[C/G]TCTCTTCAAATCGCC | 231130 |
rs213454485 | snp | A/G | | | upstream-variant-2KB | Tnip2 | Mm_Celera | 5:34514348 | AGGTTTCATTGGCTG[A/G]GCTCCTTCCTCTTCC | 231130 |
rs213550776 | snp | G/T | | | intron-variant | Tnip2 | GRCm38.p3 | 5:34509455 | CGGTTTGTTTGTTTG[G/T]TTGGTTGGTTGGTTG | 231130 |
rs213858416 | snp | C/T | | | intron-variant | Tnip2 | Mm_Celera | 5:34497407 | CAAAACCAGGGGTGG[C/T]GTGGGCAGCTGGGCA | 231130 |
rs213896399 | snp | C/T | | | missense | Tnip2 | Mm_Celera | 5:34496794 | GACCTCTCTGGGCTG[C/T]GCACACATGCCCACC | 231130 |
rs213899605 | in-del | -/AAAT | | | intron-variant | Tnip2 | Mm_Celera | 5:34501170 | TATCAAAAAACAAAC[-/AAAT]AAACTTTGCAGATCC | 231130 |
rs213902524 | snp | A/G | | | intron-variant | Tnip2 | Mm_Celera | 5:34498271 | CCACTGCCTTGTCCT[A/G]TAGACTTAGGGAGGG | 231130 |
rs213948142 | snp | A/G | | | intron-variant | Tnip2 | Mm_Celera | 5:34506232 | GCTCTATAAAGTGTG[A/G]CAAACCAGGAAGAGA | 231130 |
rs214128354 | snp | G/T | | | intron-variant | Tnip2 | Mm_Celera | 5:34504988 | GCTCCCAATGTGCTG[G/T]GACCAGGGGTCCTTA | 231130 |
rs214376391 | snp | A/G | | | intron-variant | Tnip2 | Mm_Celera | 5:34508811 | TTCATTTAGGCTTAG[A/G]GTTAGGGTGGTCTTG | 231130 |
rs214412901 | in-del | -/GTGC | | | intron-variant | Tnip2 | Mm_Celera | 5:34500087 | GGACTAAAGGTGTGT[-/GTGC]ACCACTACCACTCGG | 231130 |
rs214495294 | snp | G/T | | | upstream-variant-2KB | Tnip2 | Mm_Celera | 5:34515060 | CATCTTGATTACAAA[G/T]CAGGAAGCAGAGGGC | 231130 |
rs214604620 | snp | G/T | | | intron-variant | Tnip2 | Mm_Celera | 5:34504152 | GCAACTTCAAGGCCC[G/T]TCTGGGCTCCATGAG | 231130 |
rs214651752 | snp | A/G | | | intron-variant | Tnip2 | Mm_Celera | 5:34511807 | TACAAAAAGGGTGGA[A/G]ATGGGAAGGAAAAAA | 231130 |
rs214693773 | snp | G/T | | | intron-variant | Tnip2 | Mm_Celera | 5:34500606 | ATGGCCGCATGGGGG[G/T]TGGGGGAGGGAGCGA | 231130 |
rs214848766 | snp | A/G | | | intron-variant | Tnip2 | Mm_Celera | 5:34512573 | TTTTTTCATCATCAG[A/G]TAGTAGCACAATTTG | 231130 |
rs214854544 | snp | A/G | | | intron-variant | Tnip2 | Mm_Celera | 5:34504330 | CAACTAGGACATCCT[A/G]TCTCAAAAGAAAATT | 231130 |
rs214892454 | snp | C/G | | | intron-variant | Tnip2 | Mm_Celera | 5:34511897 | ATTATCTTTTATCAG[C/G]TAATCTCCTCTCTTA | 231130 |
rs215228207 | snp | A/T | | | intron-variant | Tnip2 | Mm_Celera | 5:34508265 | TTTTCACTTTTTTTT[A/T]TAAGACAAAATCTGA | 231130 |
rs215360396 | snp | A/T | | | intron-variant | Tnip2 | Mm_Celera | 5:34510897 | ACAGATAGAAAACCA[A/T]GACAACAGAAGTGTG | 231130 |
rs215442757 | snp | A/C | | | intron-variant | Tnip2 | Mm_Celera | 5:34510204 | TTCAATTCCCAGCAA[A/C]CACATGGTGGCCCAC | 231130 |
rs215681906 | snp | A/C | | | intron-variant | Tnip2 | Mm_Celera | 5:34499993 | ATTTCCCCATGTAGC[A/C]CTGGCTGTCCTGGAA | 231130 |
rs215717085 | snp | C/T | | | intron-variant | Tnip2 | Mm_Celera | 5:34508097 | AGAGCACTGGCTGCT[C/T]TTCCAGAGGGCATGA | 231130 |
rs215803514 | snp | C/T | | | intron-variant | Tnip2 | Mm_Celera | 5:34507537 | ATCGCCTTCAACACA[C/T]AGTTCATTTCTAGTT | 231130 |
rs215838344 | snp | A/T | | | upstream-variant-2KB | Tnip2 | Mm_Celera | 5:34514406 | GGGACACTGACCCAG[A/T]AAGGTGTTCCCATCC | 231130 |
rs215936651 | snp | C/T | | | intron-variant | Tnip2 | Mm_Celera | 5:34502096 | CAAGCTGCTGATACC[C/T]GTGTATCCCTTTCCT | 231130 |
rs216173709 | in-del | -/GG | | | intron-variant | Tnip2 | Mm_Celera | 5:34505195 | ACCCTGTCTGGGGAC[-/GG]GGGTTGGGGGAGACT | 231130 |
rs216255721 | snp | C/T | | | intron-variant | Tnip2 | Mm_Celera | 5:34505752 | TAAATGAGATCCCCA[C/T]CACACTGTAAAGACA | 231130 |
rs216290861 | snp | C/T | | | intron-variant | Tnip2 | Mm_Celera | 5:34505092 | CTTTGATCCCACACT[C/T]GGGAGGCAGAGGCAG | 231130 |
rs216495449 | in-del | -/TTTTTT | | | intron-variant | Tnip2 | Mm_Celera | 5:34500512 | TCCTGATGGCAATTC[-/TTTTTT]TTTTTTTTTTTTTTT | 231130 |
rs216633652 | snp | A/G | | | intron-variant | Tnip2 | Mm_Celera | 5:34502048 | TGAAATCTGAGATGG[A/G]TGGTTGTTGATCGAG | 231130 |
rs216672995 | snp | A/G | | | intron-variant | Tnip2 | Mm_Celera | 5:34501469 | ATACCCAGCATCCAG[A/G]AGGCTTTTTCAGGTC | 231130 |
rs216746176 | snp | A/G | | | intron-variant | Tnip2 | Mm_Celera | 5:34509511 | TTTGGGGTTTTTTTA[A/G]AGACAGGGTTTCTCT | 231130 |
rs216778916 | snp | C/T | | | intron-variant | Tnip2 | Mm_Celera | 5:34508905 | TTTCTTAAAGAATTG[C/T]GTTTATTTATTAATT | 231130 |
rs216907860 | snp | C/T | | | intron-variant | Tnip2 | Mm_Celera | 5:34499146 | ATAAAAGAAGAAAAC[C/T]CATCTAAAGGGAGAA | 231130 |
rs217063678 | snp | C/T | | | intron-variant | Tnip2 | Mm_Celera | 5:34498157 | TGATCTAAAACAAGA[C/T]GGGGAAACATGCACA | 231130 |
rs217083596 | snp | A/G | | | intron-variant | Tnip2 | Mm_Celera | 5:34505908 | TCAACAGGCTTGTAC[A/G]GAAAGCACTTTCTGC | 231130 |
rs217114670 | in-del | -/TT | | | intron-variant | Tnip2 | Mm_Celera | 5:34506098 | CCAACCATAAAATTA[-/TT]TTTTGTTGTTGTTGT | 231130 |
rs217172720 | snp | A/G | | | intron-variant | Tnip2 | Mm_Celera | 5:34505207 | GACGGGGGTTGGGGG[A/G]GACTTTTTCTGGGTT | 231130 |