SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs3661812 | snp | C/T | 0.433884 | 0.169371 | intron-variant | Gak | Mm_Celera | 5:108581126 | ATCTCCAGGTATAAG[C/T]AGGAAGTAACCTGCT | 231580 |
rs3661859 | snp | A/G | 0.455 | 0.143091 | intron-variant | Gak | Mm_Celera | 5:108581155 | CTAGCCCAGCGTACA[A/G]TCCAAGGGACCAATG | 231580 |
rs3682429 | snp | A/G | 0.5 | 0 | intron-variant, upstream-variant-2KB | Tmem175, Gak | Mm_Celera | 5:108630390 | AAGCCATATGAAGTT[A/G]CAGAGCCTTGGGTAG | 231580 |
rs3691543 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Gak | Mm_Celera | 5:108579961 | TCTATGCAACTTGAG[A/G]TGCTTTGAGTGGCTG | 231580 |
rs4137568 | snp | A/G | 0.415225 | 0.187619 | intron-variant, upstream-variant-2KB | Tmem175, Gak | Mm_Celera | 5:108630533 | TCTTTAAAAAGTCAA[A/G]TAGAAAAGAAATGAA | 231580 |
rs6271231 | snp | C/T | 0.456747 | 0.140554 | intron-variant | Gak | Mm_Celera | 5:108573398 | GAAGAGCTGCTCTGC[C/T]TTACACTCCACTGCG | 231580 |
rs6286929 | snp | C/T | 0.5 | 0 | intron-variant | Gak | Mm_Celera | 5:108580616 | GGGCAATTGATTATA[C/T]ACAGGCAAGGACTTA | 231580 |
rs6286989 | snp | A/G | 0.456747 | 0.140554 | intron-variant | Gak | Mm_Celera | 5:108580658 | ATTTGTCTTCATGAA[A/G]AAGGAAATACATGGA | 231580 |
rs6289704 | snp | A/G | 0.5 | 0 | intron-variant | Gak | Mm_Celera | 5:108581150 | ACCTGCTAGCCCAGC[A/G]TACANTCCAANGGAC | 231580 |
rs6289720 | snp | G/T | 0.5 | 0 | intron-variant | Gak | Mm_Celera | 5:108581161 | CAGCGTACAGTCCAA[G/T]GGACCAATGTGGCTA | 231580 |
rs6354472 | snp | A/G | 0.5 | 0 | intron-variant | Gak | Mm_Celera | 5:108590380 | GGAGTTGTGACCTGT[A/G]GCATGCTCTGTCTAG | 231580 |
rs6375445 | snp | G/T | 0.48 | 0.0979796 | intron-variant, upstream-variant-2KB | Tmem175, Gak | Mm_Celera | 5:108630789 | TGGGAAAGAGTGAAG[G/T]CTTTCCAGTATAGTG | 231580 |
rs6376504 | snp | A/T | 0.456747 | 0.140554 | intron-variant, upstream-variant-2KB | Tmem175, Gak | Mm_Celera | 5:108630968 | TAACTTTATGTTATT[A/T]CTGGAATGAAGTTGA | 231580 |
rs6377651 | snp | A/T | 0.415225 | 0.187619 | intron-variant, upstream-variant-2KB | Tmem175, Gak | Mm_Celera | 5:108631235 | TTTATGGCATTGTAG[A/T]AGATGCCATTCCAAG | 231580 |
rs6394905 | snp | A/C | 0.5 | 0 | intron-variant | Gak | Mm_Celera | 5:108620082 | TCACAGATATTATCC[A/C]TATCTTTCAAACCAA | 231580 |
rs6394958 | snp | A/G | 0.297521 | 0.245442 | intron-variant | Gak | Mm_Celera | 5:108620109 | CCAAGATTTCCAAAA[A/G]CCAAGATTTGCATCA | 231580 |
rs13466431 | snp | C/T | | | missense, downstream-variant-500B | Gak | Mm_Celera | 5:108571892 | CGAGAAGAGAGGGGC[C/T]TCCGTGTGCCCAGCT | 231580 |
rs13466433 | snp | C/T | 0.391111 | 0.206368 | utr-variant-3-prime, downstream-variant-500B | Gak | GRCm38.p3 | 5:108569267 | CCAATACCATCTTCA[C/T]TGAGCATTTTGCTAA | 231580 |
rs29505758 | snp | A/G | 0.465374 | 0.126941 | intron-variant | Gak | Mm_Celera | 5:108612554 | TCAAACTCCAACAGT[A/G]CTCGAGAATGAAACC | 231580 |
rs29508790 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Gak | Mm_Celera | 5:108609274 | GTGAAGAGCAGGGAG[A/G]AAAGAGAAGGAAGCT | 231580 |
rs29512827 | snp | A/G | 0.375 | 0.216506 | intron-variant | Gak | Mm_Celera | 5:108593161 | CACCTGGTGCCCTGG[A/G]AGACCATAAGACCTG | 231580 |
rs29515860 | snp | A/G | 0.487535 | 0.077957 | intron-variant | Gak | Mm_Celera | 5:108610273 | TATACATACAGAACT[A/G]AGACCCACTAGGCCC | 231580 |
rs29517416 | snp | A/G | 0.465374 | 0.126941 | intron-variant | Gak | Mm_Celera | 5:108613146 | CAAATTGCTGTTTAG[A/G]ATGACAGACAAATTC | 231580 |
rs29525292 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Gak | Mm_Celera | 5:108626363 | AAAATATAAAACAGG[A/T]GGGCTATAGGACACA | 231580 |
rs29525922 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Gak | GRCm38.p3 | 5:108598544 | GTGTGTGTGTGTGTG[C/T]GCGCATACGCATGCA | 231580 |
rs29543778 | snp | A/G | 0.487535 | 0.077957 | intron-variant | Gak | Mm_Celera | 5:108570699 | TACAGTGGTTTGTGG[A/G]CAGAACTGAGAACCT | 231580 |
rs29545943 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Gak | Mm_Celera | 5:108627691 | ACTCCCAAGAAGCTA[A/G]GGTTACAGGCCTGTG | 231580 |
rs29550204 | snp | A/G | 0.498615 | 0.0262793 | intron-variant | Gak | Mm_Celera | 5:108611012 | GCTCTGCCCACTCTG[A/G]ATTAAAAGGATTAGG | 231580 |
rs29555494 | snp | A/G | 0.5 | 0 | upstream-variant-2KB, intron-variant | Tmem175, Gak | Mm_Celera | 5:108628725 | TCCTGTACCTTATAC[A/G]AGGTCACTACAGAAA | 231580 |
rs29561034 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Gak | Mm_Celera | 5:108598160 | GCCACAGAGCATATG[C/T]ATGTGGAGGACAGAG | 231580 |
rs29568275 | snp | A/G | 0.465374 | 0.126941 | intron-variant | Gak | Mm_Celera | 5:108587211 | AAACTTCTGATTTGC[A/G]TCATGACTGTAGCAT | 231580 |
rs29572388 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Gak | Mm_Celera | 5:108579414 | TTCATCCTAAAGATG[C/T]CTGGAAGGTTCGACA | 231580 |
rs29580540 | snp | A/G | 0.487535 | 0.077957 | utr-variant-3-prime, downstream-variant-500B | Gak | Mm_Celera | 5:108569208 | TGGGAGAAACCCAAT[A/G]TTGTGGATCAGGCTC | 231580 |
rs29581060 | snp | C/T | 0.444444 | 0.157135 | upstream-variant-2KB, intron-variant | Tmem175, Gak | Mm_Celera | 5:108627888 | CCACAGGTCTTCTAC[C/T]AAAATCACATCCAAA | 231580 |
rs29626559 | snp | A/G | 0.46875 | 0.121031 | intron-variant | Gak | Mm_Celera | 5:108591576 | ACGACTGGCACAAAC[A/G]CTTATGGAACAACAG | 231580 |
rs29629469 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Gak | Mm_Celera | 5:108602610 | TCCATCTTGGCTTCC[C/T]TTGGTGATGATGAAC | 231580 |
rs29633399 | snp | A/G | 0.487535 | 0.077957 | intron-variant | Gak | Mm_Celera | 5:108611371 | ACTCTAAGAACAGAT[A/G]TGTGCTCATCTGCAC | 231580 |
rs29635131 | snp | A/G | 0.42 | 0.183303 | intron-variant | Gak | Mm_Celera | 5:108614180 | ATGAGTCATAAAATC[A/G]CATGCCATCCTAATT | 231580 |
rs29678167 | snp | A/G | 0.46875 | 0.121031 | intron-variant | Gak | Mm_Celera | 5:108625338 | AAAAGCAAGTATCCT[A/G]AAAACAAGTAACACT | 231580 |
rs29678971 | snp | A/G | 0.456747 | 0.140554 | intron-variant | Gak | Mm_Celera | 5:108591892 | TCTGGATGTTTATGT[A/G]CCAAGTTATACCAAG | 231580 |
rs29682080 | snp | C/G | 0.487535 | 0.077957 | intron-variant | Gak | Mm_Celera | 5:108609705 | ACGAAAAGAATCAAG[C/G]CAAAACATTCACCCA | 231580 |
rs29684427 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Gak | Mm_Celera | 5:108585244 | GAGGTACTGCCCAGC[C/T]TTAGGCAGAACTCTG | 231580 |
rs29685804 | snp | C/T | 0.5 | 0 | intron-variant | Gak | Mm_Celera | 5:108590435 | AACAAGAACACAACA[C/T]GGCAGGGGGCATAGC | 231580 |
rs29717931 | snp | C/T | 0.492188 | 0.0620098 | intron-variant | Gak | Mm_Celera | 5:108591247 | AAGACCAGCAGGAGA[C/T]GCATTCAGAGTGCAT | 231580 |
rs29726605 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Gak | Mm_Celera | 5:108618113 | TCTTAAAAATTTTTA[C/T]TGCAGGTGTGAGTGA | 231580 |
rs29727337 | snp | C/G | 0.489796 | 0.070696 | intron-variant | Gak | Mm_Celera | 5:108595494 | AGTGACACTATGTCA[C/G]TGTACCTCCACGAGA | 231580 |
rs29727656 | snp | A/G | 0.432133 | 0.171253 | intron-variant | Gak | Mm_Celera | 5:108619041 | CAACCTCGGACTTCA[A/G]AAATGCCTTTAGTAA | 231580 |
rs29731128 | snp | C/T | 0.49827 | 0.0293608 | intron-variant | Gak | Mm_Celera | 5:108609609 | GTCCCTCCCACTGTG[C/T]TCTGACCTCTGCTCA | 231580 |
rs29732514 | snp | C/T | 0.5 | 0 | intron-variant | Gak | Mm_Celera | 5:108572985 | TCAGAGTTTATTTCC[C/T]TGGCTATTACAAATA | 231580 |
rs29736017 | snp | C/T | 0.465374 | 0.126941 | intron-variant | Gak | Mm_Celera | 5:108617536 | CTGCTGCCAACTCCA[C/T]TCTGGTTCCATTTCC | 231580 |
rs29770248 | snp | A/T | 0.46875 | 0.121031 | intron-variant | Gak | Mm_Celera | 5:108610693 | ATGTACTTTCATTAG[A/T]AAGTTGATTTGCATA | 231580 |
rs29816463 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Gak | Mm_Celera | 5:108586447 | GCCACATACTCTTGG[C/T]CCTAAGGGAGCCTCT | 231580 |
rs29818640 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Gak | Mm_Celera | 5:108607803 | TGATCCCTTCTTGTG[A/G]TTTGTTCTAATTACC | 231580 |
rs29822716 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Gak | Mm_Celera | 5:108584780 | ACCCCAAAAGTAGGT[A/C]AAGGATTCATATACT | 231580 |
rs29823632 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Gak | Mm_Celera | 5:108592066 | CATAACTCCTCTTTC[A/C]CCACCCTCAGCCCAA | 231580 |
rs29825187 | snp | A/G | 0.5 | 0 | intron-variant | Gak | Mm_Celera | 5:108595047 | TCAGAGTCTACCCAA[A/G]AGTCTGAGATTCTCA | 231580 |
rs33040953 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Gak | Mm_Celera | 5:108591022 | TACAATCAGCGTCAC[A/G]TGGTAGGTCTCTCAC | 231580 |
rs33054228 | snp | A/C/T | 0.459184 | 0.136902 | intron-variant | Gak | GRCm38.p3 | 5:108599584 | TTTAAGAAGAGCCTA[A/C/T]GTCCTAGAATACTGA | 231580 |
rs33067368 | snp | A/C/G | 0.48 | 0.0979796 | intron-variant | Gak | GRCm38.p3 | 5:108593473 | GTTTTGTTTTGTTTT[A/C/G]TTCTGTTTGTTTTTT | 231580 |
rs33075693 | snp | A/G | 0.5 | 0 | intron-variant | Gak | Mm_Celera | 5:108610280 | ACAGAACTAAGACCC[A/G]CTAGGCCCCCCAGAA | 231580 |
rs33076153 | snp | C/T | 0.444444 | 0.157135 | intron-variant, downstream-variant-500B | Gak | Mm_Celera | 5:108571568 | AAAAACAAAACAACA[C/T]TCTTCTAGACACTGT | 231580 |
rs33098098 | snp | C/T | 0.475309 | 0.108333 | intron-variant | Gak | Mm_Celera | 5:108609813 | AGCTTACGTGAGGGG[C/T]ACTATTCTAATGAGC | 231580 |
rs33098641 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Gak | Mm_Celera | 5:108616471 | TCTACAAAGTGAGTT[C/T]CAGGACAGCCAGGGC | 231580 |
rs33106980 | snp | A/G | 0.492188 | 0.0620098 | intron-variant | Gak | Mm_Celera | 5:108605342 | AGATCCCTATGCACG[A/G]ATGAGGACTCGGACC | 231580 |
rs33114778 | snp | A/G | 0.495 | 0.0497494 | intron-variant, downstream-variant-500B | Gak | Mm_Celera | 5:108571133 | CCCAAACAAATTGCT[A/G]CTGTCAACAGTCAGA | 231580 |
rs33120553 | snp | A/C | 0.489796 | 0.070696 | intron-variant | Gak | Mm_Celera | 5:108596683 | CTGCAGGTCCGACAC[A/C]GTGAAGGCAGCAGCA | 231580 |
rs33131548 | snp | C/G | 0.5 | 0 | intron-variant | Gak | Mm_Celera | 5:108579560 | AAGTTTTGGAGAGAT[C/G]AGGGATAAAAGGGAC | 231580 |
rs33133175 | snp | C/T | 0.290657 | 0.246672 | intron-variant | Gak | Mm_Celera | 5:108600849 | CTCTACACAGTATAC[C/T]TTAACCTCTAACCCA | 231580 |
rs33151194 | snp | A/T | 0.5 | 0 | intron-variant | Gak | Mm_Celera | 5:108625877 | TGTCTCTAAAGGACC[A/T]ACAGCAGCAGTACTA | 231580 |
rs33156822 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Gak | Mm_Celera | 5:108592050 | TGTATACACTCTTGT[A/T]CATAACTCCTCTTTC | 231580 |
rs33157832 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Gak | Mm_Celera | 5:108603047 | TTCCTCGAACCCACC[A/C]GTGAACTGTCTTTCC | 231580 |
rs33189400 | snp | C/T | 0.465374 | 0.126941 | intron-variant | Gak | Mm_Celera | 5:108617583 | CATTCACAGAATCTA[C/T]ACAAACCTAAAGGAA | 231580 |
rs33223774 | snp | C/T | 0.465374 | 0.126941 | downstream-variant-500B | Gak | Mm_Celera | 5:108568670 | CAGGAGTGTGTCTGG[C/T]TAAGATAAACCTGGG | 231580 |
rs33234046 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Gak | Mm_Celera | 5:108598546 | GTGTGTGTGTGTGCG[C/T]GCATACGCATGCACA | 231580 |
rs33236647 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Gak | Mm_Celera | 5:108591017 | AGCTTTACAATCAGC[A/G]TCACATGGTAGGTCT | 231580 |
rs33259908 | snp | A/T | 0.48 | 0.0979796 | intron-variant | Gak | Mm_Celera | 5:108609039 | TTTTTTAAGATTTAT[A/T]AACTTATGTGTATGA | 231580 |
rs33260861 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Gak | Mm_Celera | 5:108618018 | CATGGGCACTAGGCA[C/T]GCATATATCTGTATA | 231580 |
rs33273832 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Gak | Mm_Celera | 5:108627064 | AGCCTTAAAATATCA[C/T]ATTAAGTATAAAAAG | 231580 |
rs33276557 | snp | G/T | 0.277778 | 0.248452 | intron-variant | Gak | Mm_Celera | 5:108621063 | ACTACAGGAATTCAT[G/T]AAGACAAAATGTAGC | 231580 |
rs33277917 | snp | A/G | 0.5 | 0 | intron-variant | Gak | Mm_Celera | 5:108589452 | AACCTGAATTAAGAA[A/G]TCAGAGAATAACCTG | 231580 |
rs33278076 | snp | A/C | 0.495 | 0.0497494 | intron-variant | Gak | Mm_Celera | 5:108572190 | GGCCATGTGCTCGTA[A/C]AACAAGCCACTATCA | 231580 |
rs33299867 | snp | C/G/T | 0.5 | 0 | intron-variant | Gak | Mm_Celera | 5:108596540 | ACAAGTCAGAAGCCA[C/G/T]CACAGCTTCAGAGTT | 231580 |
rs33301337 | snp | C/T | 0.197531 | 0.244432 | downstream-variant-500B | Gak | Mm_Celera | 5:108568850 | TTTGAAGCAGTCTTA[C/T]ACACCCCATCTGTAC | 231580 |
rs33306143 | snp | A/T | 0.48 | 0.0979796 | intron-variant | Gak | Mm_Celera | 5:108578960 | CCTCTTTTGGTTTTT[A/T]GAGACAGGGTTTCTC | 231580 |
rs33308040 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | Gak | Mm_Celera | 5:108596355 | ATTTTGTGACCGCAG[A/G]GAAGCAGGGTAATAA | 231580 |
rs33314456 | snp | C/T | 0.444444 | 0.157135 | upstream-variant-2KB, intron-variant | Tmem175, Gak | Mm_Celera | 5:108627852 | GTGGAGGTCCTAAAC[C/T]CATCTCTGGCGGGAA | 231580 |
rs33317045 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Gak | Mm_Celera | 5:108602002 | GGCATCCTTGGGCAG[C/T]AGGAGCATCCATACT | 231580 |
rs33317407 | snp | A/G | 0.5 | 0 | intron-variant | Gak | Mm_Celera | 5:108596224 | CAGGCTAAGCTTCAG[A/G]TTGGATTCCTGTGTC | 231580 |
rs33323166 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Gak | Mm_Celera | 5:108586822 | GGATGGAAGAACAAG[A/G]CAGGAGAGCCCACGG | 231580 |
rs33341222 | snp | A/T | 0.401235 | 0.199068 | intron-variant | Gak | Mm_Celera | 5:108602350 | CTTGTGATTGTTAGA[A/T]TTTGGTCTTGTCTTG | 231580 |
rs33352508 | snp | C/T | 0.456747 | 0.140554 | intron-variant | Gak | Mm_Celera | 5:108585788 | GGGAGGCCAGGTGCT[C/T]AGAGTGACCACAGAA | 231580 |
rs33355795 | snp | A/G | 0.5 | 0 | synonymous-codon, nc-transcript-variant | Gak | Mm_Celera | 5:108583126 | GAGAGGTATTGTCTA[A/G]CCCAGTCTCTGGTTC | 231580 |
rs33378570 | snp | A/G | 0.49827 | 0.0293608 | intron-variant | Gak | Mm_Celera | 5:108596312 | CCTACTTATGGCAAC[A/G]GGAATGTCTGAGTGA | 231580 |
rs33388527 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Gak | Mm_Celera | 5:108602473 | AAGACTAGCCTATGG[A/G]CAGGTGGTCCTGGGC | 231580 |
rs33403102 | snp | C/T | 0.188366 | 0.242283 | intron-variant | Gak | Mm_Celera | 5:108586555 | CAAAGCAATGGTTCG[C/T]TTCATTTACTATTAT | 231580 |
rs33414334 | snp | A/G | 0.498615 | 0.0262793 | intron-variant | Gak | Mm_Celera | 5:108608962 | TTGCATATGATATCC[A/G]TGCAGACGCAGAGTC | 231580 |
rs33421820 | snp | C/T | 0.444444 | 0.157135 | intron-variant, downstream-variant-500B | Gak | Mm_Celera | 5:108582663 | TCTGCATAACTGAAA[C/T]GCATACCAGTGTCAG | 231580 |
rs33422101 | snp | C/T | 0.415225 | 0.187619 | intron-variant | Gak | Mm_Celera | 5:108584446 | AAGGCACAGTCAGAA[C/T]ACAGGATAGAGTAGG | 231580 |
rs33424845 | snp | C/G | 0.432133 | 0.171253 | intron-variant | Gak | Mm_Celera | 5:108609637 | TCACTCACCTGGCCA[C/G]GCAATGCTGTACCAT | 231580 |
rs33430330 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Gak | Mm_Celera | 5:108598123 | AACCTCTGTGTGCCC[A/G]TGTATATGCATACAC | 231580 |