SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs6162507 | snp | C/G | 0.5 | 0 | utr-variant-3-prime, downstream-variant-500B | Ing2 | Mm_Celera | 8:47667288 | TTTTCTAGGTTGATC[C/G]ATCACCCAANATTCA | 69260 |
rs6162857 | snp | C/T | 0.5 | 0 | utr-variant-3-prime, downstream-variant-500B | Ing2 | GRCm38.p3 | 8:47667298 | TGATCNATCACCCAA[C/T]ATTCAGGTAAGGTGA | 69260 |
rs6164420 | snp | A/G | 0.5 | 0 | utr-variant-3-prime | Ing2 | GRCm38.p3 | 8:47667618 | ATTATTAATCGTATT[A/G]TTATAATGAAATTAG | 69260 |
rs48451296 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Ing2 | Mm_Celera | 8:47669381 | TGCCATATTAGCACA[C/T]ACATCATTTTCAAGT | 69260 |
rs49662480 | snp | A/G | | | intron-variant | Ing2 | Mm_Celera | 8:47672856 | ATGTCTGCAGAAAAT[A/G]CCACAGAATGATTTT | 69260 |
rs50049547 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Ing2 | Mm_Celera | 8:47671530 | AGCCATCTTGTTGGC[C/T]TGTGCATTTCACGTT | 69260 |
rs212133111 | snp | A/T | | | intron-variant | Ing2 | Mm_Celera | 8:47670112 | CTGGCACCCACAGAA[A/T]ACATGGTGTGGCTGT | 69260 |
rs212422375 | snp | C/T | | | intron-variant | Ing2 | Mm_Celera | 8:47670855 | TATCTAACTCAGCAG[C/T]TGAGTCAATGCTTGC | 69260 |
rs212557781 | snp | C/T | | | upstream-variant-2KB | Ing2 | Mm_Celera | 8:47676405 | CAAGGGAAACCTAGG[C/T]CCTGGTCTAGATGAA | 69260 |
rs212761345 | in-del | -/AA | | | intron-variant, upstream-variant-2KB | Ing2 | Mm_Celera | 8:47674429 | CACACACACACACAC[-/AA]AACCGCTTCCCGGCC | 69260 |
rs212879131 | snp | C/G | | | upstream-variant-2KB | Ing2 | Mm_Celera | 8:47675862 | GTGGCAAGGCTGCAC[C/G]CCGCCCCGGTCCCCA | 69260 |
rs213857217 | snp | A/G | | | intron-variant, upstream-variant-2KB | Ing2 | GRCm38.p3 | 8:47673937 | AGCCGAAGAAGGGCT[A/G]AGTGAGACACCGGGC | 69260 |
rs214048634 | snp | C/G | | | intron-variant | Ing2 | Mm_Celera | 8:47670092 | ATGAGGACCTAAGCT[C/G]ACTCCTGGCACCCAC | 69260 |
rs214354724 | in-del | -/A | | | intron-variant, upstream-variant-2KB | Ing2 | Mm_Celera | 8:47673369 | ACAATCCCTGAAGAT[-/A]ATTCCCTGTCCTAGT | 69260 |
rs214587745 | snp | A/C | | | intron-variant | Ing2 | Mm_Celera | 8:47672691 | CTGAACAGTTTATGA[A/C]AATTACAGGTAACTG | 69260 |
rs214903441 | snp | A/C | | | utr-variant-3-prime | Ing2 | GRCm38.p3 | 8:47668432 | TGCAGTTCGTTCATA[A/C]GCCTCTCTGCCTGCT | 69260 |
rs215018650 | snp | A/C | | | upstream-variant-2KB | Ing2 | Mm_Celera | 8:47676763 | CTGGCTGTCCTGGAG[A/C]TCACTCTCTAGACCA | 69260 |
rs215417208 | in-del | -/TT | | | upstream-variant-2KB | Ing2 | Mm_Celera | 8:47675964 | ACAGTCCTCACTGTC[-/TT]TTCACTCGGCTTCAC | 69260 |
rs215532532 | in-del | -/TTAG | | | intron-variant | Ing2 | Mm_Celera | 8:47669990 | GGATCAACATAAACC[-/TTAG]TTAGGGTCATTCACC | 69260 |
rs215671031 | in-del | -/T | | | intron-variant | Ing2 | Mm_Celera | 8:47670770 | CCAGAGTAGATCTGC[-/T]GTTGCTGGCATCCAG | 69260 |
rs215817982 | snp | A/G | | | utr-variant-3-prime | Ing2 | Mm_Celera | 8:47668042 | GTCTGTTCTGAAGAA[A/G]CAGGGGCTTTTACAG | 69260 |
rs215998163 | snp | C/T | | | intron-variant | Ing2 | Mm_Celera | 8:47670888 | ACGCTGCTGATGCAA[C/T]GGTATTAAAAGTTGA | 69260 |
rs216022243 | snp | A/G | | | intron-variant | Ing2 | Mm_Celera | 8:47672647 | TTGCATTAACCTCTC[A/G]GTCTTGTAAGATCTA | 69260 |
rs216054549 | snp | C/T | | | upstream-variant-2KB | Ing2 | Mm_Celera | 8:47675730 | GGTAGGCGGTGCGCC[C/T]TCTGCCCTTTTAAAT | 69260 |
rs216355532 | snp | C/G | | | upstream-variant-2KB | Ing2 | Mm_Celera | 8:47676723 | GTTTGGTTTTGATTT[C/G]GAGACAGGGTTTCTC | 69260 |
rs217680442 | snp | A/G | | | intron-variant | Ing2 | Mm_Celera | 8:47672863 | CAGAAAATACCACAG[A/G]ATGATTTTCATTTTT | 69260 |
rs217716109 | snp | A/G | | | intron-variant, upstream-variant-2KB | Ing2 | GRCm38.p3 | 8:47674136 | GGAGGGAGCCCCAGC[A/G]GGCAAGGGGCTAAGC | 69260 |
rs218709062 | in-del | -/C | | | intron-variant | Ing2 | Mm_Celera | 8:47671097 | CCCATGTTTTAGCTT[-/C]CAATGGTATTACTAT | 69260 |
rs218982735 | snp | C/T | | | upstream-variant-2KB | Ing2 | Mm_Celera | 8:47676837 | GTGCTGAGTTAAAGG[C/T]GTGTGCCACCACTGC | 69260 |
rs219045325 | in-del | -/CC | | | upstream-variant-2KB | Ing2 | GRCm38.p3 | 8:47676177 | TTTGGTTTTGGTTCT[-/CC]CCCCCCCCCCCAACC | 69260 |
rs219557918 | in-del | -/T | | | utr-variant-3-prime | Ing2 | Mm_Celera | 8:47667366 | AAAAAAACATCTTTC[-/T]TTTTTTTTTTTTTCC | 69260 |
rs220044852 | in-del | -/G | | | intron-variant | Ing2 | Mm_Celera | 8:47671806 | TTAACTATACAGTGA[-/G]GGGGAAAAAAAAGCA | 69260 |
rs220193159 | snp | C/T | | | synonymous-codon | Ing2 | Mm_Celera | 8:47669164 | CAGCTCCATTTGTCT[C/T]GCTCGGTTCTCCACC | 69260 |
rs220358305 | in-del | -/GGGG | | | intron-variant, upstream-variant-2KB | Ing2 | GRCm38.p3 | 8:47673593 | TTCACTAACCGGGGT[-/GGGG]GGGGGGGCTAGGGAG | 69260 |
rs220710421 | snp | C/T | | | intron-variant | Ing2 | Mm_Celera | 8:47671273 | AGTAATACTTGATGG[C/T]CAATTTTGCCACAAG | 69260 |
rs220746962 | snp | A/G | | | intron-variant | Ing2 | Mm_Celera | 8:47672925 | TCCTGTGTGAGTCCT[A/G]ACTTCAATCTCTTGG | 69260 |
rs220798534 | in-del | -/C | | | upstream-variant-2KB | Ing2 | Mm_Celera | 8:47676192 | CCCCCCCCCCCCCAA[-/C]CGAAATAGGTATAAG | 69260 |
rs220851320 | snp | A/G | | | downstream-variant-500B | Ing2 | Mm_Celera | 8:47667065 | CTTACTAAGAAGAAA[A/G]ATGATAGTCACCAAG | 69260 |
rs220984503 | snp | C/T | | | intron-variant, upstream-variant-2KB | Ing2 | Mm_Celera | 8:47673102 | TGGTGAAAACACTGT[C/T]ATACTATAAACAGTG | 69260 |
rs221046972 | snp | A/G | | | intron-variant, upstream-variant-2KB | Ing2 | Mm_Celera | 8:47674391 | GGCCGCGAGTGTGCT[A/G]TGCCGTCCCCCCACC | 69260 |
rs221211283 | snp | G/T | | | upstream-variant-2KB | Ing2 | Mm_Celera | 8:47676101 | TCAGTGAAATGCCGG[G/T]AGGAGGAGCTCACTG | 69260 |
rs221634282 | snp | A/G | | | intron-variant | Ing2 | Mm_Celera | 8:47669469 | AACTCTACATCATCC[A/G]ATATGAAAGTATACT | 69260 |
rs221659426 | snp | A/G | | | intron-variant | Ing2 | Mm_Celera | 8:47670195 | TAGCTTCAGTGAGAG[A/G]CCCGCCTCCAAAACA | 69260 |
rs221904070 | snp | G/T | | | upstream-variant-2KB | Ing2 | Mm_Celera | 8:47675911 | GAAACTGTTGTCAGA[G/T]GTCGAATCGCCTAGG | 69260 |
rs222301456 | snp | A/G | | | intron-variant | Ing2 | Mm_Celera | 8:47669737 | CTCAGCTGTGAAAAT[A/G]TCTCAAAACCCTGGG | 69260 |
rs222450262 | snp | G/T | | | intron-variant | Ing2 | Mm_Celera | 8:47670394 | AAGTTAAGACAAATG[G/T]ATTACATAAGACATG | 69260 |
rs222709039 | in-del | -/A | | | utr-variant-3-prime | Ing2 | Mm_Celera | 8:47668098 | CTACCAAGAAAATAC[-/A]GCAGTGGACACTCCA | 69260 |
rs222734439 | snp | A/C | | | upstream-variant-2KB | Ing2 | Mm_Celera | 8:47677201 | AAACTTTGTGAACTT[A/C]AAACATGATAATGTG | 69260 |
rs222853730 | snp | A/G | | | intron-variant | Ing2 | Mm_Celera | 8:47671046 | AAAAAATAAATAAAT[A/G]AACAGTAGCTCTTAG | 69260 |
rs223177711 | snp | A/T | | | intron-variant | Ing2 | Mm_Celera | 8:47670544 | TGCAGCCACAGATTG[A/T]TACTAAATTATGTGT | 69260 |
rs223189655 | snp | C/T | | | upstream-variant-2KB | Ing2 | Mm_Celera | 8:47676454 | ACACAACGCGGAATT[C/T]GGCGTCCTGAGGACA | 69260 |
rs223217396 | snp | G/T | | | intron-variant | Ing2 | Mm_Celera | 8:47671179 | ATAAGTGCATGATGC[G/T]GGCTATCTGACAGCA | 69260 |
rs223226572 | snp | A/G | | | upstream-variant-2KB | Ing2 | Mm_Celera | 8:47676040 | TCAACCACCGAGTGC[A/G]GTGCTTTCCGTGTGA | 69260 |
rs223244446 | snp | C/G | | | downstream-variant-500B | Ing2 | Mm_Celera | 8:47666971 | GCATCAGTAAAAGAG[C/G]TACATTCAAGAGGGA | 69260 |
rs223326983 | snp | A/C | | | upstream-variant-2KB | Ing2 | Mm_Celera | 8:47677484 | CTCCCACTCTACACT[A/C]TAGAAATTGATGCTA | 69260 |
rs223663404 | in-del | -/C | | | upstream-variant-2KB | Ing2 | Mm_Celera | 8:47675777 | CGTGCGGCCCCTCCA[-/C]CCCCCCAGCGCCGGG | 69260 |
rs223919861 | in-del | -/AGGGCT | | | upstream-variant-2KB | Ing2 | Mm_Celera | 8:47676470 | GGCGTCCTGAGGACA[-/AGGGCT]ATATTGGAAGGCCTG | 69260 |
rs224477326 | snp | G/T | | | utr-variant-5-prime, upstream-variant-2KB, intron-variant | Ing2 | Mm_Celera | 8:47674962 | CCGGCCCCCTCCCTC[G/T]CTAGGAGAGCGAGCA | 69260 |
rs224608791 | snp | A/T | | | missense, upstream-variant-2KB, intron-variant | Ing2 | GRCm38.p3 | 8:47674605 | CCTGCACGTAGCAGG[A/T]GAGCAGCCGGCTCCG | 69260 |
rs227234272 | snp | C/G | | | intron-variant | Ing2 | Mm_Celera | 8:47669945 | TCTCCGACAGAAACC[C/G]AAAGACAAAGCCAAT | 69260 |
rs227355464 | snp | A/C | | | intron-variant | Ing2 | Mm_Celera | 8:47670610 | ATGACTCCAGAGAGA[A/C]ACATTACCTTAATTT | 69260 |
rs227726933 | in-del | -/A | | | intron-variant | Ing2 | Mm_Celera | 8:47672778 | TTTGCGCTTTTAAAG[-/A]AAAAAAACTACATAT | 69260 |
rs228198207 | in-del | -/T | | | upstream-variant-2KB | Ing2 | Mm_Celera | 8:47677165 | AACTCCAGATCCCTG[-/T]TTTTCCACTGGCACT | 69260 |
rs228214849 | snp | A/C | | | intron-variant, upstream-variant-2KB | Ing2 | GRCm38.p3 | 8:47673688 | GCCCAGCAATGGGTT[A/C]AGTCCACCCCAGGAC | 69260 |
rs228627483 | snp | A/G | | | intron-variant | Ing2 | Mm_Celera | 8:47671645 | AAAATAAAGACATTA[A/G]CTATTTCCTTGTTAG | 69260 |
rs228774303 | snp | A/G | | | upstream-variant-2KB, intron-variant | Ing2 | Mm_Celera | 8:47675372 | CCCCCTCTTAAAGGG[A/G]CCGCATGGCTGAGCC | 69260 |
rs228835902 | snp | A/G | | | utr-variant-5-prime, upstream-variant-2KB, intron-variant | Ing2 | Mm_Celera | 8:47675087 | GTCGCCCGGATCCCC[A/G]TGACAAGCCCCTCGC | 69260 |
rs228892821 | snp | C/T | | | upstream-variant-2KB | Ing2 | Mm_Celera | 8:47676236 | TTAATTCAGATGAGA[C/T]GCCCAATGGGAGCGG | 69260 |
rs228918673 | snp | A/G | | | intron-variant | Ing2 | Mm_Celera | 8:47669843 | TATGTTTTAGTTCCT[A/G]CCTCCCGGTTCCTGC | 69260 |
rs229061366 | snp | A/G | | | intron-variant | Ing2 | Mm_Celera | 8:47670825 | TCAAGTCAGCACTGG[A/G]CCATTCTCCCTTTGT | 69260 |
rs229429965 | snp | C/T | | | intron-variant | Ing2 | Mm_Celera | 8:47672006 | AACTCAATGACCTCC[C/T]ATATTAAAATAAAGA | 69260 |
rs229618815 | snp | A/G | | | upstream-variant-2KB | Ing2 | Mm_Celera | 8:47675885 | GGTCCCCAGTCCCAA[A/G]CCATCTTAAGGAAAC | 69260 |
rs229690131 | in-del | -/CAAT | | | intron-variant | Ing2 | Mm_Celera | 8:47670345 | AATGTACCAAACTAA[-/CAAT]CAAAAGTATTTCACA | 69260 |
rs229723666 | snp | C/T | | | intron-variant, upstream-variant-2KB | Ing2 | GRCm38.p3 | 8:47674020 | CGCCACGCCGGGAGC[C/T]GGAGGGGGGTGGGGG | 69260 |
rs229828850 | snp | C/T | | | utr-variant-3-prime | Ing2 | Mm_Celera | 8:47667378 | TTTCTTTTTTTTTTT[C/T]TCCAAACAAGCAGAT | 69260 |
rs230879022 | in-del | -/AAAAAAAAC | | | upstream-variant-2KB | Ing2 | Mm_Celera | 8:47677071 | AAAAAAAAAAAAAAA[-/AAAAAAAAC]CAAGTTGAGAAGCAA | 69260 |
rs231141870 | snp | C/T | | | upstream-variant-2KB | Ing2 | Mm_Celera | 8:47676300 | TGCTAAGTTTGGGTG[C/T]TCTTGCCCGGTTTGC | 69260 |
rs231510545 | snp | A/G | | | upstream-variant-2KB | Ing2 | Mm_Celera | 8:47677260 | GCTGCATTTATTCAT[A/G]CAGGTTAATCTAATT | 69260 |
rs231727553 | snp | G/T | | | intron-variant, upstream-variant-2KB | Ing2 | GRCm38.p3 | 8:47673747 | CCCGCGGGAGCGCGC[G/T]CCCCGCCCATACGAC | 69260 |
rs232189658 | snp | C/G | | | intron-variant | Ing2 | Mm_Celera | 8:47672650 | CATTAACCTCTCAGT[C/G]TTGTAAGATCTACTA | 69260 |
rs232795954 | in-del | -/AC | | | upstream-variant-2KB | Ing2 | Mm_Celera | 8:47675945 | CACCCGCCAGCGAGG[-/AC]ACACAGTCCTCACTG | 69260 |
rs233103786 | snp | C/G | | | intron-variant | Ing2 | Mm_Celera | 8:47670336 | ACATATACAAATGTA[C/G]CAAACTAACAATCAA | 69260 |
rs233221113 | snp | A/G | | | intron-variant | Ing2 | Mm_Celera | 8:47670903 | TGGTATTAAAAGTTG[A/G]ACACTTTTAAATCAA | 69260 |
rs233366424 | in-del | -/CA | | | intron-variant, upstream-variant-2KB | Ing2 | GRCm38.p3 | 8:47673825 | ACTCACACACACACG[-/CA]CACACACACACGGAC | 69260 |
rs233546473 | snp | C/T | | | upstream-variant-2KB | Ing2 | Mm_Celera | 8:47675932 | ATCGCCTAGGCATCA[C/T]CCGCCAGCGAGGACA | 69260 |
rs233581276 | snp | A/T | | | upstream-variant-2KB | Ing2 | Mm_Celera | 8:47676739 | GAGACAGGGTTTCTC[A/T]GTGTAGCCCTGGCTG | 69260 |
rs233715155 | snp | C/T | | | utr-variant-3-prime | Ing2 | Mm_Celera | 8:47668152 | GGAGCATGGGTACTG[C/T]TGTCTCTAGTTCCTG | 69260 |
rs233747609 | in-del | -/T | | | intron-variant, upstream-variant-2KB | Ing2 | Mm_Celera | 8:47673249 | AATGACTCCAAGTTG[-/T]TTTTTATGGTCCATA | 69260 |
rs233883206 | snp | A/G | | | utr-variant-3-prime | Ing2 | Mm_Celera | 8:47667834 | CCCACTGACGGGTCT[A/G]TGGCTAAACATCCCA | 69260 |
rs234994478 | snp | C/T | | | downstream-variant-500B | Ing2 | Mm_Celera | 8:47666679 | TCTCCCAAAGGTTTT[C/T]GATAGGCTGAAAATT | 69260 |
rs235236456 | snp | A/C | | | intron-variant | Ing2 | Mm_Celera | 8:47670113 | TGGCACCCACAGAAA[A/C]CATGGTGTGGCTGTG | 69260 |
rs235276031 | snp | C/T | | | intron-variant | Ing2 | Mm_Celera | 8:47670864 | CAGCAGTTGAGTCAA[C/T]GCTTGCTGACGCTGC | 69260 |
rs235374685 | snp | A/G | | | intron-variant | Ing2 | Mm_Celera | 8:47672884 | TTTCATTTTTTGAAA[A/G]GGTGAACTTGTAGGG | 69260 |
rs235673049 | snp | A/T | | | intron-variant | Ing2 | Mm_Celera | 8:47672735 | CCCTGTCAAAAAATT[A/T]TGTCACTACCAATCT | 69260 |
rs235791044 | snp | A/G | | | intron-variant, upstream-variant-2KB | Ing2 | GRCm38.p3 | 8:47674159 | GGCTAAGCAGGCCCA[A/G]CACCCCGGTCCAGCC | 69260 |
rs236044837 | snp | C/T | | | upstream-variant-2KB | Ing2 | Mm_Celera | 8:47676777 | GCTCACTCTCTAGAC[C/T]AGACTGGCCTCAAAC | 69260 |
rs236056236 | in-del | -/TGAATTC | | | downstream-variant-500B | Ing2 | Mm_Celera | 8:47666782 | AAGTCATATTCCAAA[-/TGAATTC]TGTATCTCAATTGCT | 69260 |
rs236226326 | snp | A/C | | | intron-variant, upstream-variant-2KB | Ing2 | Mm_Celera | 8:47674429 | ACACACACACACACA[A/C]AACCGCTTCCCGGCC | 69260 |
rs236409865 | snp | C/T | | | intron-variant | Ing2 | Mm_Celera | 8:47670101 | TAAGCTGACTCCTGG[C/T]ACCCACAGAAAACAT | 69260 |
rs236484356 | in-del | -/C | | | upstream-variant-2KB | Ing2 | Mm_Celera | 8:47677320 | GGGAAAATGTTTACT[-/C]GAGGATGGGAAGTAG | 69260 |