SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs6221454 | snp | C/T | 0.5 | 0 | intron-variant | Taf5l | GRCm38.p3 | 8:123998680 | ACAGCCACCAGCCAA[C/T]CATGGATGCCAAGAG | 102162 |
rs6221956 | snp | C/T | 0.5 | 0 | intron-variant | Taf5l | GRCm38.p3 | 8:123998770 | GATACTGCAGAGACT[C/T]TGGGGGAAAAAGCAA | 102162 |
rs6223063 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Taf5l | GRCm38.p3 | 8:123998955 | AAACACAGCCTGACC[A/G]ACAGAGAGTAAGACT | 102162 |
rs6223217 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Taf5l | GRCm38.p3 | 8:123999037 | TCATGCCACCCTTGG[A/G]TTAATTTTCCCATGG | 102162 |
rs6224298 | snp | C/T | 0.5 | 0 | intron-variant | Taf5l | GRCm38.p3 | 8:123999209 | ACCGAGCTTTGTTGG[C/T]TCCTGCATCGAAAAA | 102162 |
rs6224855 | snp | A/G | 0.5 | 0 | intron-variant | Taf5l | GRCm38.p3 | 8:123999296 | ATAATTGCTTCTAAT[A/G]TGTGCGGACTTGAGG | 102162 |
rs13459284 | snp | A/T | 0.5 | 0 | utr-variant-3-prime | Taf5l | GRCm38.p3 | 8:123996739 | CTCCTGCAGGGATGG[A/T]GGCAAAGGAGGTTCT | 102162 |
rs13459285 | snp | C/T | 0.5 | 0 | utr-variant-3-prime | Taf5l | GRCm38.p3 | 8:123996983 | GAAAGGAGGGGATGA[C/T]GTCTTTCCTTTTCCA | 102162 |
rs31825334 | snp | A/G | 0.124444 | 0.216185 | synonymous-codon | Taf5l | Mm_Celera | 8:124003154 | CAGCTGTTCCGTGTT[A/G]TAGAAGGCATAGAAG | 102162 |
rs31825337 | snp | C/T | 0.124444 | 0.216185 | synonymous-codon | Taf5l | Mm_Celera | 8:124003382 | GTGCACGGCAAGCAC[C/T]TTGCACAGGGCAGTG | 102162 |
rs31825340 | snp | A/G | 0.124444 | 0.216185 | synonymous-codon | Taf5l | Mm_Celera | 8:124003406 | GGCAGTGTTGTTGTC[A/G]CTTTGGAGGTAGCGG | 102162 |
rs31825343 | snp | A/G | 0.456747 | 0.140554 | intron-variant | Taf5l | GRCm38.p3 | 8:124003826 | ATGGAAGAGCAGACT[A/G]TGAGGTTCAGTCAAG | 102162 |
rs31826136 | snp | A/G | 0.290657 | 0.246672 | intron-variant | Taf5l | GRCm38.p3 | 8:124003902 | TAGGCCTACAGCGTA[A/G]GATCTTCTTCGTTAC | 102162 |
rs31826139 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Taf5l | GRCm38.p3 | 8:124003913 | CGTAAGATCTTCTTC[A/G]TTACTTAAGTCAGAA | 102162 |
rs31826141 | snp | A/C | 0.375 | 0.216506 | intron-variant | Taf5l | GRCm38.p3 | 8:124003931 | ACTTAAGTCAGAAAC[A/C]CATACTTCTGAGAAT | 102162 |
rs31826894 | snp | A/G | 0.456747 | 0.140554 | intron-variant | Taf5l | GRCm38.p3 | 8:124004769 | GCCCAAAGTGTGCCG[A/G]GTCGAGCTTTACTGA | 102162 |
rs31826897 | snp | C/G | 0.152778 | 0.230321 | intron-variant | Taf5l | Mm_Celera | 8:124004809 | GAGAAGAGGTGCACA[C/G]GGCACATCAGTGTGG | 102162 |
rs31826900 | snp | C/T | 0.46875 | 0.121031 | intron-variant | Taf5l | GRCm38.p3 | 8:124004897 | CAGCCACCATGGCAG[C/T]GCTAGACACTTGAGG | 102162 |
rs31826903 | snp | A/G | 0.475309 | 0.108333 | intron-variant | Taf5l | GRCm38.p3 | 8:124005106 | TATTTAAAAAGAGCC[A/G]TTTCACAGCAGGAGC | 102162 |
rs31827726 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Taf5l | Mm_Celera | 8:124005291 | CTTTTTGGCTCTCTC[C/T]ACCAGCAAGATGCCC | 102162 |
rs31827729 | snp | A/T | 0.493827 | 0.0552116 | intron-variant | Taf5l | GRCm38.p3 | 8:124005435 | CCAGCCCAAAAGAGA[A/T]CTAACACACTTCGTC | 102162 |
rs31827732 | snp | A/G | 0.465374 | 0.126941 | intron-variant | Taf5l | GRCm38.p3 | 8:124005718 | GTGAAGAACAAGAAG[A/G]CTCAGCTGGTGGTGA | 102162 |
rs31828595 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Taf5l | GRCm38.p3 | 8:124005767 | CCATTGAGCTGGTGG[A/T]TTTCCTGCCTGCCCT | 102162 |
rs31828598 | snp | A/G | 0.475309 | 0.108333 | intron-variant | Taf5l | GRCm38.p3 | 8:124006673 | GCCAGGTTTCACAGC[A/G]AGTATCTTTTTGCCT | 102162 |
rs31828601 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Taf5l | Mm_Celera | 8:124007272 | AAGGGAACACGTCCA[A/T]GATTTTGTCTCCTTG | 102162 |
rs31829414 | snp | C/T | 0.304688 | 0.243945 | intron-variant | Taf5l | Mm_Celera | 8:124007304 | TCACTCTATGGCCTA[C/T]GTAAATGACAATAGC | 102162 |
rs31829417 | snp | A/G | 0.493827 | 0.0552116 | intron-variant | Taf5l | GRCm38.p3 | 8:124008376 | GGGAGAGCACAGAGC[A/G]CAATGGCATCTCTCA | 102162 |
rs31829420 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Taf5l | Mm_Celera | 8:124008399 | ATCTCTCAGTAGTCT[C/T]TAGGACCCTGACAGA | 102162 |
rs31829423 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Taf5l | Mm_Celera | 8:124008547 | AGAGAAGAGAAGAGA[A/G]GCACGCAATATTCCT | 102162 |
rs31829429 | snp | A/T | 0.444444 | 0.157135 | downstream-variant-500B | Taf5l | Mm_Celera | 8:123996258 | TCTGCCCACTACTCT[A/T]GGTCCAGTGATGCAC | 102162 |
rs31829432 | snp | A/G | 0.5 | 0 | utr-variant-3-prime | Taf5l | GRCm38.p3 | 8:123996649 | TGGGTAACTGGTGCA[A/G]CGCTGAGGCCTACCC | 102162 |
rs31830055 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Taf5l | Mm_Celera | 8:123999634 | GAACCAGGGCTGTGG[C/T]AACCTTCCTCAAGCC | 102162 |
rs31830058 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Taf5l | GRCm38.p3 | 8:123999953 | AGCTCTTGTCCTCAG[C/T]TTTCAGCATGTGAAG | 102162 |
rs31830061 | snp | A/G | 0.375 | 0.216506 | intron-variant | Taf5l | GRCm38.p3 | 8:124000177 | TCTGCTGCATAGCAC[A/G]AGAGACCACCGGGGA | 102162 |
rs31830196 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Taf5l | Mm_Celera | 8:124008890 | GATGTGAAACAGGGC[A/T]CCACAGGGATGATGG | 102162 |
rs31830199 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Taf5l | Mm_Celera | 8:124009494 | GACAGAAAACAATCT[A/G]GACTCTCTGAGGAAA | 102162 |
rs31830202 | snp | A/T | 0.487535 | 0.077957 | intron-variant | Taf5l | Mm_Celera | 8:124009512 | CTCTCTGAGGAAAGA[A/T]ACACGGCTCTAGCAG | 102162 |
rs31830904 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Taf5l | GRCm38.p3 | 8:124000282 | CTTAGCTTATCCAGT[A/G]AAACAGTGTCCATAT | 102162 |
rs31830907 | snp | A/G | 0.473373 | 0.11227 | intron-variant | Taf5l | GRCm38.p3 | 8:124001119 | AACTGTTAGGTCTGA[A/G]CACTGAATTAATCGG | 102162 |
rs31830910 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Taf5l | GRCm38.p3 | 8:124001487 | GTGGTGCCATTTTAT[A/G]CTGAACTGTCATTTG | 102162 |
rs31830913 | snp | A/G | 0.495868 | 0.0452663 | intron-variant | Taf5l | Mm_Celera | 8:124001697 | GCTGTGCTCCTGACT[A/G]CCCTAGCCTGACAGG | 102162 |
rs31830995 | snp | A/G | 0.33241 | 0.236027 | intron-variant | Taf5l | GRCm38.p3 | 8:124009608 | AGAGCTGCTCACTGA[A/G]GCTTGGTAGCCTACC | 102162 |
rs31830998 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Taf5l | Mm_Celera | 8:124010243 | GAGCTGAGAACCTGG[C/T]AATGGGAAGTTCCCT | 102162 |
rs31831001 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Taf5l | GRCm38.p3 | 8:124010302 | CGAACAGCCAGGAAG[C/T]ACTGCACCAGTGAGC | 102162 |
rs31831786 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Taf5l | Mm_Celera | 8:124002717 | CACACTCGAGTACAT[A/G]TGACAGACACGTAAT | 102162 |
rs31831789 | snp | G/T | 0.336735 | 0.234472 | intron-variant | Taf5l | GRCm38.p3 | 8:124002934 | AAGGGAACTACAGAT[G/T]ACTGTTTCAGTCAGT | 102162 |
rs31831874 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Taf5l | GRCm38.p3 | 8:124013426 | AATTGATAACACGAA[C/T]GGTGGTGTGTCCAGG | 102162 |
rs31831877 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Taf5l | GRCm38.p3 | 8:124013647 | AGTACCAAAGGCAAC[A/G]GAATGAACTTAGGTT | 102162 |
rs31831880 | snp | C/T | 0.35503 | 0.226867 | intron-variant | Taf5l | Mm_Celera | 8:124013742 | GGATCCGTTCTCCAC[C/T]CTCCTTAGTGCAGCC | 102162 |
rs31831883 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Taf5l | GRCm38.p3 | 8:124013975 | CACACAACTGCCATG[C/T]CCTTCTGGATTAAAA | 102162 |
rs31832666 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Taf5l | Mm_Celera | 8:124014498 | ATGAGGGAAAAGACT[C/G]TAAAGCTGTAAAAGA | 102162 |
rs32554971 | snp | G/T | 0.5 | 0 | intron-variant | Taf5l | GRCm38.p3 | 8:124016921 | GGTCTACATAGCAAG[G/T]TCTAGAATAGCCAGA | 102162 |
rs32575936 | snp | A/T | 0.5 | 0 | intron-variant | Taf5l | GRCm38.p3 | 8:124015813 | TGACACGGACACACC[A/T]GGGGTTTTGGGGATG | 102162 |
rs32576521 | snp | C/T | 0.5 | 0 | upstream-variant-2KB, intron-variant | Urb2, Taf5l, Mir1967 | GRCm38.p3 | 8:124022340 | ACAGGAAGGGAGGCC[C/T]CTCAGTTCTGAAGGC | 102162 |
rs32577440 | snp | A/G | 0.444444 | 0.157135 | upstream-variant-2KB, intron-variant | Urb2, Taf5l, Mir1967 | GRCm38.p3 | 8:124022429 | GTTCTGTCAGGGTTT[A/G]AGCTAAGTTGTTTAC | 102162 |
rs32623138 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Taf5l | GRCm38.p3 | 8:124015546 | TGTATCTCAGCCTCA[C/T]CCACTTACCATCAAA | 102162 |
rs32624520 | snp | C/T | 0.444444 | 0.157135 | upstream-variant-2KB, downstream-variant-500B, intron-variant | Urb2, Taf5l, Mir1967 | GRCm38.p3 | 8:124023220 | GCTCAAAGTTAGGAG[C/T]ACAGCTGCTCTCAGA | 102162 |
rs32627338 | snp | A/T | 0.444444 | 0.157135 | utr-variant-3-prime | Taf5l | Mm_Celera | 8:123996310 | ATAAGATGCCACACA[A/T]TTTTTTTGAAACTAA | 102162 |
rs32640443 | snp | A/G | 0.5 | 0 | intron-variant | Taf5l | GRCm38.p3 | 8:124017265 | TGGAGTGACTGACAC[A/G]TTGCCTCCAACCCTT | 102162 |
rs32662074 | snp | C/T | 0.5 | 0 | intron-variant | Taf5l | GRCm38.p3 | 8:124001132 | GAACACTGAATTAAT[C/T]GGCTATTGTACCAAA | 102162 |
rs32712522 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Taf5l | GRCm38.p3 | 8:124005980 | GGGGAGGTAACCTGG[G/T]TCCTAAGTCTGTGGC | 102162 |
rs32725642 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Taf5l | GRCm38.p3 | 8:124017730 | CTTTGTAGACCAGGC[C/T]GGCCTCGAACTCACA | 102162 |
rs32774052 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Taf5l | GRCm38.p3 | 8:124017736 | AGACCAGGCTGGCCT[C/T]GAACTCACAGATTCA | 102162 |
rs32780216 | snp | A/G | 0.5 | 0 | intron-variant | Taf5l | GRCm38.p3 | 8:124000308 | CATATCAGGTTAACA[A/G]CCCCTTATAACAGAT | 102162 |
rs32783064 | snp | C/T | 0.5 | 0 | intron-variant | Taf5l | GRCm38.p3 | 8:124000506 | AGGACCTTGACATAT[C/T]AGGCCTTACTTTTTT | 102162 |
rs32787166 | snp | C/T | 0.5 | 0 | intron-variant | Taf5l | GRCm38.p3 | 8:124006579 | GTGTGTGTGTCAGGT[C/T]ATGTGTGTAGAGGGC | 102162 |
rs32805525 | snp | C/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | Taf5l, Urb2 | GRCm38.p3 | 8:124019899 | ACTTGCCCAAAGTCA[C/T]GCAGTTCCTGAATGG | 102162 |
rs32810291 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Taf5l | GRCm38.p3 | 8:124006402 | CTGGTGCCTTCAAAC[A/G]CCAGAAGAGGGTACA | 102162 |
rs32827065 | snp | A/G | 0.5 | 0 | intron-variant | Taf5l | GRCm38.p3 | 8:124004669 | CCAGCCTGGTCTACA[A/G]AGTGAGTTCCAGGAC | 102162 |
rs32844990 | snp | C/T | 0.375 | 0.216506 | intron-variant | Taf5l | GRCm38.p3 | 8:124016154 | TCTCCTTATCTCCTG[C/T]CTTAATCCACCTTTC | 102162 |
rs32845007 | snp | C/G/T | 0.5 | 0 | intron-variant | Taf5l | GRCm38.p3 | 8:124007832 | AGAATTGACATTACT[C/G/T]GATGGTATTAAAATG | 102162 |
rs32857068 | snp | C/T | 0.5 | 0 | intron-variant | Taf5l | GRCm38.p3 | 8:124000684 | TACAGATTCTGGGGA[C/T]GAAGCACAGGTTGCC | 102162 |
rs32870543 | snp | G/T | 0.444444 | 0.157135 | upstream-variant-2KB, nc-transcript-variant, intron-variant | Urb2, Taf5l, Mir1967 | GRCm38.p3 | 8:124022708 | ATCCTGGGGAGAAGA[G/T]GCAGAATTCCCTGGA | 102162 |
rs32882324 | snp | A/G | 0.5 | 0 | intron-variant | Taf5l | GRCm38.p3 | 8:123998563 | TTAGGAAAAACCTGA[A/G]CTCAAAGGCCAGCTA | 102162 |
rs32928274 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Taf5l | GRCm38.p3 | 8:124018188 | AGTTGAGCCCCAGTA[A/C]AGCCAAGGCAATGTA | 102162 |
rs32929921 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Taf5l | GRCm38.p3 | 8:124011274 | GGTGCCAAGCCTCAA[A/C]TCCTTTGCATGACCC | 102162 |
rs32932019 | snp | A/G | 0.444444 | 0.157135 | upstream-variant-2KB, intron-variant | Urb2, Taf5l, Mir1967 | GRCm38.p3 | 8:124022394 | ACAGTCTCTTGCCTC[A/G]ACACAGCAGCGTGGT | 102162 |
rs32939328 | snp | C/T | 0.5 | 0 | intron-variant | Taf5l | GRCm38.p3 | 8:124018900 | TCCATCCCCTTGTCA[C/T]GGCCGGTTGCAGTAG | 102162 |
rs32968521 | snp | C/T | 0.5 | 0 | intron-variant | Taf5l | GRCm38.p3 | 8:123999724 | CTAGTGTGGCTCAGC[C/T]CATGACCACACAGGC | 102162 |
rs32978747 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Taf5l | GRCm38.p3 | 8:124010124 | CTTCTGCTGCTCTGT[C/T]AGAGAGCTGGTACCA | 102162 |
rs32995285 | snp | A/T | 0.5 | 0 | intron-variant | Taf5l | GRCm38.p3 | 8:124018937 | AAGAACAAGCCTCCA[A/T]TTCCACATTAGTTTG | 102162 |
rs33000103 | snp | A/G | 0.444444 | 0.157135 | upstream-variant-2KB, nc-transcript-variant, intron-variant | Urb2, Taf5l, Mir1967 | GRCm38.p3 | 8:124022683 | CTCCTTTTGTCTGAC[A/G]TTCATGAGGATCCTG | 102162 |
rs33003841 | snp | A/T | 0.375 | 0.216506 | intron-variant | Taf5l | GRCm38.p3 | 8:124012416 | GGCAAGTCTTTTTTT[A/T]TAAAAAAAGATTTAT | 102162 |
rs33059073 | snp | C/G | 0.5 | 0 | intron-variant | Taf5l | GRCm38.p3 | 8:124004342 | CACCTTAAAACAAAA[C/G]AAAAAAAAAAACTTC | 102162 |
rs33066539 | snp | C/T | 0.5 | 0 | intron-variant | Taf5l | GRCm38.p3 | 8:124004649 | GCTGATTTCTGAGTT[C/T]GAGGCCAGCCTGGTC | 102162 |
rs33071556 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Taf5l | GRCm38.p3 | 8:124015431 | CCAGAAAGGAAAGAC[C/T]GCTGGCTCCCTGCTC | 102162 |
rs33075529 | snp | A/C | 0.48 | 0.0979796 | intron-variant | Taf5l | GRCm38.p3 | 8:124010289 | GGACCCAGAGCCTCG[A/C]ACAGCCAGGAAGCAC | 102162 |
rs33117335 | snp | C/T | 0.5 | 0 | intron-variant | Taf5l | GRCm38.p3 | 8:124006462 | TAACTACTTCATGGG[C/T]GACAGGATCCGAACC | 102162 |
rs33137366 | snp | A/T | 0.5 | 0 | intron-variant | Taf5l | Mm_Celera | 8:124007791 | CCTTATTTGTGTTTA[A/T]TGTATTGTTGCTTGT | 102162 |
rs33143638 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Taf5l | GRCm38.p3 | 8:124019128 | GAAGACCATCTTGGT[A/G]TTGGAGCAACAACTA | 102162 |
rs33145789 | snp | C/T | 0.5 | 0 | synonymous-codon | Taf5l | GRCm38.p3 | 8:123997945 | ATGTCCCTGATACAG[C/T]ACAGTGTTGGTGAAG | 102162 |
rs33166615 | snp | A/G | 0.444444 | 0.157135 | downstream-variant-500B | Taf5l | GRCm38.p3 | 8:123996234 | CTCTGTGTCTCATCT[A/G]GCTTATGCTCTGCCC | 102162 |
rs33185768 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Taf5l | GRCm38.p3 | 8:124015669 | CCATCTCTACCTCCA[A/C]ACCTGACTGCCTTCC | 102162 |
rs33203119 | snp | A/G | 0.5 | 0 | intron-variant | Taf5l | Mm_Celera | 8:124017502 | CTTTTGATCTTTTGT[A/G]ATTTCTAGAAATACG | 102162 |
rs33255819 | snp | C/T | 0.5 | 0 | intron-variant | Taf5l | GRCm38.p3 | 8:124018999 | GAGACATGATCCCAG[C/T]ACTCCTCAGTGAACA | 102162 |
rs33272388 | snp | C/T | 0.375 | 0.216506 | intron-variant, upstream-variant-2KB | Taf5l, Mir1967, Urb2 | GRCm38.p3 | 8:124020677 | GCAACTCTAAGTCTC[C/T]GCGGTCACCAACTCC | 102162 |
rs33276161 | snp | A/G | 0.5 | 0 | intron-variant | Taf5l | GRCm38.p3 | 8:124018701 | TCCTCACAGCACTTC[A/G]TCCTTTCCAAATCCC | 102162 |
rs33277634 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Taf5l | GRCm38.p3 | 8:124017895 | CCATGAGTATCACGG[C/T]GAGGAGCAGACAAGC | 102162 |
rs33288737 | snp | A/T | 0.5 | 0 | intron-variant | Taf5l | Mm_Celera | 8:124004180 | CTGTCTCAAAAAATC[A/T]TCTGGGGCTAGAGAG | 102162 |
rs33330859 | snp | A/T | 0.375 | 0.216506 | intron-variant | Taf5l | Mm_Celera | 8:124012417 | GCAAGTCTTTTTTTT[A/T]AAAAAAAGATTTATT | 102162 |