SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs3091124 | snp | C/T | 0.21875 | 0.248039 | intron-variant, utr-variant-3-prime, downstream-variant-500B | Inppl1, Phox2a | Mm_Celera | 7:101822501 | TAGCTGGGCCACTCA[C/T]TCCTTGAAATCAAGC | 16332 |
rs3682265 | snp | C/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | Inppl1, LOC102639173 | GRCm38.p3 | 7:101836181 | CACACACTATTCAAC[C/T]CCACCCTACAATCAT | 16332 |
rs3710141 | snp | A/G | 0.5 | 0 | intron-variant | Inppl1 | GRCm38.p3 | 7:101832126 | GTAAGCTCTGCCGGC[A/G]AGAAATAAGGGTGGT | 16332 |
rs3726315 | snp | C/G | 0.48 | 0.0979796 | intron-variant | Inppl1 | GRCm38.p3 | 7:101832389 | TAGGAACAGGGTACA[C/G]TGGAGGAAGTCAGGA | 16332 |
rs3726958 | snp | C/T | 0.48 | 0.0979796 | synonymous-codon, nc-transcript-variant | Inppl1 | GRCm38.p3 | 7:101832492 | GTGTAGCCTTCGGCA[C/T]GAGGTGACAAGGGTT | 16332 |
rs13471179 | snp | C/T | 0.5 | 0 | synonymous-codon, nc-transcript-variant | Inppl1 | GRCm38.p3 | 7:101824487 | CAGCTTCAATAACCC[C/T]GCCTACTACGTCCTT | 16332 |
rs31096073 | snp | A/G | 0.375 | 0.216506 | downstream-variant-500B, intron-variant, upstream-variant-2KB | Folr2, Inppl1, LOC102639173 | GRCm38.p3 | 7:101839842 | TTCCTACAGGCTACT[A/G]AAGCACAGACGCTCG | 16332 |
rs31180321 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Inppl1 | GRCm38.p3 | 7:101826874 | CCAGTGAGGATAATC[C/T]CCTAGATGCCCCATC | 16332 |
rs31235074 | snp | A/T | 0.375 | 0.216506 | upstream-variant-2KB, downstream-variant-500B, intron-variant | Inppl1, LOC102639173 | GRCm38.p3 | 7:101839465 | AGCTAAGCAGACACA[A/T]GATGGGAATAGGGAA | 16332 |
rs31243612 | snp | C/T | 0.375 | 0.216506 | missense, nc-transcript-variant | Inppl1 | GRCm38.p3 | 7:101824195 | CACGGGCCTCACCCC[C/T]ACTTCGGCCCCTGAC | 16332 |
rs31248754 | snp | C/T | 0.375 | 0.216506 | downstream-variant-500B, intron-variant, upstream-variant-2KB | Folr2, Inppl1, LOC102639173 | GRCm38.p3 | 7:101839910 | ACATTTGTATAGTGA[C/T]GGTGAGTTTTGAAAC | 16332 |
rs31256504 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Inppl1 | GRCm38.p3 | 7:101827821 | GTCTGATGCCCTCTT[C/T]TGGTGTGTCTGAAGA | 16332 |
rs31260803 | snp | A/G | 0.444444 | 0.157135 | intron-variant, upstream-variant-2KB | Inppl1, LOC102639173 | GRCm38.p3 | 7:101835594 | ACTTAGTGTGGAACT[A/G]TGGGGCAGGGAGTAG | 16332 |
rs31326561 | snp | A/G | 0.375 | 0.216506 | intron-variant, upstream-variant-2KB | Inppl1, LOC102639173 | GRCm38.p3 | 7:101835365 | CTACTAGCCTTTGGA[A/G]CCACCAAATCCTTTG | 16332 |
rs31360758 | snp | C/G | 0.375 | 0.216506 | intron-variant | Inppl1 | GRCm38.p3 | 7:101834228 | CAATGTGCTAACACA[C/G]GCCTGAGACTCTGTC | 16332 |
rs31403120 | snp | A/C | 0.375 | 0.216506 | intron-variant | Inppl1 | Mm_Celera | 7:101830618 | GTATACATAATAAAT[A/C]TTAAAATAAAAAATA | 16332 |
rs31526645 | snp | C/T | 0.375 | 0.216506 | upstream-variant-2KB, downstream-variant-500B, intron-variant | Inppl1, Folr2, LOC102639173 | GRCm38.p3 | 7:101839799 | TTTAAAAATCCTGGA[C/T]CTTCCTGTTATTTGA | 16332 |
rs31546197 | snp | C/T | 0.5 | 0 | intron-variant | Inppl1 | GRCm38.p3 | 7:101824666 | ACTGGCACTTGACCT[C/T]GAGTAAGTCACTTGC | 16332 |
rs31555444 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Inppl1 | GRCm38.p3 | 7:101829085 | CAGAGGCTCGCCTCT[C/T]GAGAAAGGTGATACA | 16332 |
rs31678254 | snp | C/T | 0.5 | 0 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | Inppl1, Phox2a | GRCm38.p3 | 7:101822750 | CCACCTTTCTGAGTG[C/T]CCAAGGTGGGATAAA | 16332 |
rs31773047 | snp | A/C | 0.375 | 0.216506 | intron-variant | Inppl1 | Mm_Celera | 7:101834072 | CTACAGAGACTCTAC[A/C]CCCACCACAGGGCAA | 16332 |
rs31801009 | snp | C/T | 0.375 | 0.216506 | upstream-variant-2KB, downstream-variant-500B, intron-variant | Inppl1, Folr2, LOC102639173 | Mm_Celera | 7:101839540 | TTTAATGTATATGAG[C/T]ACAATGTAGCTGTCT | 16332 |
rs31834769 | snp | A/T | 0.444444 | 0.157135 | intron-variant, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | Inppl1, LOC102639173 | GRCm38.p3 | 7:101837382 | TCCACAACTACTACA[A/T]CATCCAAGAGAACAA | 16332 |
rs31848218 | snp | A/T | 0.375 | 0.216506 | intron-variant | Inppl1 | Mm_Celera | 7:101830619 | TATACATAATAAATC[A/T]TAAAATAAAAAATAA | 16332 |
rs31947131 | snp | A/G | 0.375 | 0.216506 | intron-variant | Inppl1 | Mm_Celera | 7:101830041 | TGCAGGGGCCCACCT[A/G]CCCTTGCTTACCCAG | 16332 |
rs31968817 | snp | A/G | 0.5 | 0 | intron-variant | Inppl1 | Mm_Celera | 7:101824697 | TCTCTCCAAGCCCTT[A/G]AGGCAAAGGTAAAAC | 16332 |
rs31983801 | snp | C/G | 0.375 | 0.216506 | synonymous-codon, nc-transcript-variant | Inppl1 | GRCm38.p3 | 7:101829241 | AAAGGCACTGAGCTG[C/G]CGATCACCCAACGAG | 16332 |
rs32031865 | snp | A/T | 0.375 | 0.216506 | intron-variant | Inppl1 | Mm_Celera | 7:101830637 | AAATAAAAAATAAAT[A/T]AAAAAAAAAAAGGGA | 16332 |
rs32104799 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Inppl1 | GRCm38.p3 | 7:101826946 | AGGCTTGTCCATGTT[C/T]ACTCTTACAGACATA | 16332 |
rs32125599 | snp | A/G | 0.444444 | 0.157135 | synonymous-codon, nc-transcript-variant | Inppl1 | GRCm38.p3 | 7:101829034 | CTCTCTCCTACTAAT[A/G]TAGTTCAGGATCTCC | 16332 |
rs32130157 | snp | A/T | 0.375 | 0.216506 | intron-variant | Inppl1 | Mm_Celera | 7:101830632 | TCTTAAAATAAAAAA[A/T]AAATTAAAAAAAAAA | 16332 |
rs32195192 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Inppl1 | GRCm38.p3 | 7:101829533 | GAATGGGTCTCAGGA[A/G]AATGGAGGGTAAGCA | 16332 |
rs32204394 | snp | A/C | 0.375 | 0.216506 | intron-variant | Inppl1 | Mm_Celera | 7:101834068 | AGACCTACAGAGACT[A/C]TACACCCACCACAGG | 16332 |
rs32252642 | snp | A/G | 0.5 | 0 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | Inppl1, Phox2a | GRCm38.p3 | 7:101823156 | GTGGGGAGCTGGGGA[A/G]CACGATGTTTTAACT | 16332 |
rs32308465 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Inppl1 | GRCm38.p3 | 7:101830226 | GTCCCTACCTATACT[C/T]CCTATGCCTATCAAC | 16332 |
rs32340189 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Inppl1 | GRCm38.p3 | 7:101833255 | TGTGAATACATGTGC[A/G]TGCATGCATATGTGT | 16332 |
rs32348186 | snp | C/T | 0.5 | 0 | intron-variant | Inppl1 | GRCm38.p3 | 7:101824740 | CCCCACTTACATTCT[C/T]TCTCCGTTCTTATAA | 16332 |
rs32359882 | snp | A/T | 0.444444 | 0.157135 | intron-variant, upstream-variant-2KB | Inppl1, LOC102639173 | Mm_Celera | 7:101836164 | CCAAGTCTTCCTCCC[A/T]ACACACACTATTCAA | 16332 |
rs32412599 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Inppl1 | GRCm38.p3 | 7:101828709 | CTTGATGCCCCACTG[C/T]TAACTTCCTGAAACC | 16332 |
rs32479007 | snp | C/G | 0.375 | 0.216506 | upstream-variant-2KB, downstream-variant-500B, intron-variant | Inppl1, Folr2, LOC102639173 | Mm_Celera | 7:101839722 | AAGCTCTCCAGGCAA[C/G]CACTCTTCCAACTGA | 16332 |
rs32511314 | snp | A/T | 0.375 | 0.216506 | intron-variant | Inppl1 | Mm_Celera | 7:101830636 | AAAATAAAAAATAAA[A/T]TAAAAAAAAAAAGGG | 16332 |
rs45795605 | snp | G/T | | | intron-variant | Inppl1 | GRCm38.p3 | 7:101832799 | CAGCTGGGGAAACAA[G/T]TCTCAGAGAAGGAAC | 16332 |
rs46126243 | snp | A/G | | | intron-variant | Inppl1 | GRCm38.p3 | 7:101824986 | GGGTGATAGCAGCCT[A/G]AGAAGGGCGACTAGA | 16332 |
rs46587582 | snp | A/C | | | intron-variant | Inppl1 | Mm_Celera | 7:101825822 | CACCTTGCCCAGCTC[A/C]AGGACCAATACCTAC | 16332 |
rs47430447 | snp | A/C | | | intron-variant | Inppl1 | Mm_Celera | 7:101825532 | AAAATACTACTACTA[A/C]TACTACTACTAATAA | 16332 |
rs47487993 | snp | C/G | | | intron-variant | Inppl1 | GRCm38.p3 | 7:101831104 | GGAGAACAGGGCACA[C/G]AGTAGCCAGTCAGGG | 16332 |
rs47691746 | snp | C/G | | | intron-variant, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | Inppl1, LOC102639173 | GRCm38.p3 | 7:101837343 | CGGGATCAAGGTTCG[C/G]AAAGCAAGGCTCCAG | 16332 |
rs47886493 | snp | A/C | | | intron-variant | Inppl1 | GRCm38.p3 | 7:101828571 | ACTGACAAAATCCTA[A/C]TCTTCCTCTGTTCCT | 16332 |
rs48020077 | snp | C/T | | | upstream-variant-2KB, nc-transcript-variant | Inppl1, LOC102639173 | GRCm38.p3 | 7:101838934 | GGAGAAAAGCTGTCA[C/T]GACCCTCCAAAATCA | 16332 |
rs48305580 | snp | C/T | | | intron-variant | Inppl1 | GRCm38.p3 | 7:101825833 | GCTCCAGGACCAATA[C/T]CTACATCCAAGGCAG | 16332 |
rs49854253 | snp | C/T | | | intron-variant | Inppl1 | Mm_Celera | 7:101825453 | CTACAAAGTTAGTTC[C/T]AGGACAGCTGGGGCT | 16332 |
rs50087977 | snp | A/G | | | intron-variant | Inppl1 | GRCm38.p3 | 7:101831331 | GCTAAAGAGACTCCA[A/G]TAGCCGCCAACACCC | 16332 |
rs50247811 | snp | A/G | | | upstream-variant-2KB, downstream-variant-500B, intron-variant | Inppl1, LOC102639173 | Mm_Celera | 7:101839212 | CTAGAGGGTGCTTCT[A/G]CCTCTGGGAAGCCAC | 16332 |
rs50837995 | snp | C/T | | | intron-variant | Inppl1 | GRCm38.p3 | 7:101831257 | CGAGTGCTATCTACC[C/T]TCAACACACTCCCTG | 16332 |
rs50982978 | snp | A/T | | | intron-variant | Inppl1 | GRCm38.p3 | 7:101825686 | AATAACCTCAAGCTA[A/T]GTCCTTTTTTGTTTG | 16332 |
rs51407179 | snp | A/C | | | intron-variant | Inppl1 | Mm_Celera | 7:101825541 | CTACTACTACTACTA[A/C]TAATAAATCTAGCAA | 16332 |
rs52321857 | snp | C/T | | | intron-variant | Inppl1 | GRCm38.p3 | 7:101826467 | CCCACACCACCACAT[C/T]GCATGCCCCACCCAC | 16332 |
rs52345589 | snp | A/T | | | intron-variant | Inppl1 | Mm_Celera | 7:101825506 | AACAAACAAAAAAAA[A/T]TTTTTTTTTAAAAAT | 16332 |
rs52579135 | snp | C/T | | | intron-variant | Inppl1 | GRCm38.p3 | 7:101829866 | TCACACATGCACATG[C/T]ATACACCCACCTCTC | 16332 |
rs211771570 | in-del | -/AAC | | | cds-indel, downstream-variant-500B | Inppl1, Phox2a | GRCm38.p3 | 7:101823183 | ACTAGAATGTCCCAA[-/AAC]ACTGGGCAGTAGGGA | 16332 |
rs211895158 | snp | C/T | | | intron-variant, upstream-variant-2KB | Inppl1, LOC102639173 | Mm_Celera | 7:101835281 | ACTTGTTGCAGAAGC[C/T]GAGAGGTTCCCAGAA | 16332 |
rs212029179 | snp | C/T | | | intron-variant | Inppl1 | Mm_Celera | 7:101825876 | AGACTCACTGGGGTC[C/T]CTTTAACTCAGAGGT | 16332 |
rs212234342 | snp | C/G | | | upstream-variant-2KB, intron-variant | Inppl1, LOC102639173 | GRCm38.p3 | 7:101837855 | CGCCTCGTCCGCCCG[C/G]GTCCCGGTCTCCGCC | 16332 |
rs212241978 | snp | C/T | | | intron-variant, upstream-variant-2KB | Inppl1, LOC102639173 | Mm_Celera | 7:101835920 | TGCCCTCTTCTGGTG[C/T]CTGAAGACAGCTACA | 16332 |
rs212462600 | snp | G/T | | | intron-variant | Inppl1 | GRCm38.p3 | 7:101827207 | CATCTCTTGCTCTTT[G/T]TAATCCCTTCATCTA | 16332 |
rs212500012 | snp | C/T | | | upstream-variant-2KB, utr-variant-5-prime, intron-variant | Inppl1, LOC102639173 | Mm_Celera | 7:101837919 | GCTCTTCAGTGCGCC[C/T]GAGCTTCTCGCTTTC | 16332 |
rs213014807 | snp | A/G | | | intron-variant | Inppl1 | Mm_Celera | 7:101828661 | TTCAGGGAAGCCAGC[A/G]AAGCTTGAGTAGCAA | 16332 |
rs213059875 | snp | C/T | | | utr-variant-3-prime, upstream-variant-2KB, intron-variant | Folr2, Inppl1, LOC102639173 | Mm_Celera | 7:101839997 | CAATAATTCATTAGG[C/T]CCAGATGTGTCATAG | 16332 |
rs213259104 | snp | C/T | | | intron-variant | Inppl1 | Mm_Celera | 7:101831498 | GGAAAGAGGAGTCAC[C/T]TGTGCTATCAGACAG | 16332 |
rs213306480 | snp | A/G | | | intron-variant, upstream-variant-2KB | Inppl1, LOC102639173 | Mm_Celera | 7:101836201 | CCTACAATCATATAT[A/G]GTCGCAGAATTGCCC | 16332 |
rs213430888 | snp | C/T | | | intron-variant | Inppl1 | Mm_Celera | 7:101826987 | AGCATTTTACATCAT[C/T]ACAGTTAATTTTCTA | 16332 |
rs213464624 | snp | A/G | | | upstream-variant-2KB, intron-variant | Inppl1, LOC102639173 | GRCm38.p3 | 7:101837873 | CCCGGTCTCCGCCGC[A/G]CGCCCGCAGAGTGAC | 16332 |
rs213488384 | snp | A/C | | | intron-variant | Inppl1 | Mm_Celera | 7:101828363 | TGAGGCAGATAGTAA[A/C]CACCCAAGTGTCTCC | 16332 |
rs213632286 | in-del | -/T | | | upstream-variant-2KB, downstream-variant-500B, intron-variant | Inppl1, Folr2, LOC102639173 | Mm_Celera | 7:101839490 | AGGGAATGTGTTTTG[-/T]TTTTGTTTTTTTTTT | 16332 |
rs213987047 | snp | C/T | | | intron-variant | Inppl1 | Mm_Celera | 7:101830495 | CACTGGCTGCTCTTC[C/T]AGAGATCCTGAGTTC | 16332 |
rs214019183 | snp | C/T | | | intron-variant | Inppl1 | Mm_Celera | 7:101829502 | GAGGAAGTCAGGCCC[C/T]GGGCTATGGGGAAAG | 16332 |
rs214433352 | snp | G/T | | | intron-variant | Inppl1 | Mm_Celera | 7:101831951 | GGTAAAGGGTCCTTC[G/T]GAGGGATGTGACAGG | 16332 |
rs214490706 | snp | A/T | | | downstream-variant-500B, intron-variant, upstream-variant-2KB | Folr2, Inppl1, LOC102639173 | Mm_Celera | 7:101839918 | ATAGTGATGGTGAGT[A/T]TTGAAACACTATTTA | 16332 |
rs214554119 | snp | C/T | | | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | Inppl1, Phox2a | Mm_Celera | 7:101823107 | CTACTAACCTCCCCC[C/T]GCGCACCCCCCCCCC | 16332 |
rs214615468 | snp | C/T | | | synonymous-codon, nc-transcript-variant | Inppl1 | Mm_Celera | 7:101824298 | ATCTGGAGGAGGCAG[C/T]GTGCCCCCAGAGTCC | 16332 |
rs214887464 | snp | A/G | | | downstream-variant-500B, intron-variant, upstream-variant-2KB | Folr2, Inppl1, LOC102639173 | Mm_Celera | 7:101839901 | TTACAATGAACATTT[A/G]TATAGTGATGGTGAG | 16332 |
rs214989996 | snp | A/G | | | synonymous-codon, nc-transcript-variant | Inppl1 | Mm_Celera | 7:101832960 | TAGTGGGGGCTTCTC[A/G]TCCTCCACATCTGTG | 16332 |
rs215308536 | snp | C/T | | | intron-variant | Inppl1 | Mm_Celera | 7:101828736 | AACCTGAGGGAGATT[C/T]CCCCAGTCCATATTT | 16332 |
rs215455413 | snp | A/G | | | intron-variant | Inppl1 | Mm_Celera | 7:101831738 | GTGGAAAGGCTGCTG[A/G]CAAGACCTTACACAG | 16332 |
rs215728361 | snp | A/G | | | intron-variant | Inppl1 | Mm_Celera | 7:101829446 | GTCAGGCATAGACAA[A/G]AGGAGTCCTGAGGCA | 16332 |
rs215947494 | snp | C/T | | | intron-variant | Inppl1 | Mm_Celera | 7:101834373 | ACCCAAAGGGGATCC[C/T]GATGGGAGACTCAGC | 16332 |
rs215967621 | in-del | -/CACACACACACACA | | | intron-variant | Inppl1 | GRCm38.p3 | 7:101829777 | TTTTCCTTCCTCCAG[-/CACACACACACACA]CACACACACACACAC | 16332 |
rs215972419 | snp | A/G | | | intron-variant | Inppl1 | Mm_Celera | 7:101825283 | AAGAACAATCTACAG[A/G]GCAAGTGCAGGACAG | 16332 |
rs216008836 | snp | C/G | | | intron-variant, upstream-variant-2KB | Inppl1, LOC102639173 | Mm_Celera | 7:101835063 | CTGACAATGGAACCA[C/G]GATCTCTCTTCACTG | 16332 |
rs216213532 | snp | C/T | | | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | Inppl1, Phox2a | Mm_Celera | 7:101823012 | AGTGGAAGTGAGGAC[C/T]CAGGTGTGCCCCACG | 16332 |
rs217175941 | in-del | -/ACGAGA | | | intron-variant, upstream-variant-2KB | Inppl1, LOC102639173 | Mm_Celera | 7:101834843 | TGGCTGGTATCGAGT[-/ACGAGA]GCAGAAGCAAGTTTG | 16332 |
rs217273164 | snp | C/T | | | upstream-variant-2KB, intron-variant, utr-variant-5-prime, nc-transcript-variant | Inppl1, LOC102639173 | GRCm38.p3 | 7:101837833 | GCCTTCCGCCCCGCC[C/T]GCGCCCCGCCTCGTC | 16332 |
rs217305983 | snp | A/G | | | intron-variant, upstream-variant-2KB | Inppl1, LOC102639173 | Mm_Celera | 7:101836035 | CCCACATGAAGGCTT[A/G]CAACCATCTGTACAG | 16332 |
rs217608052 | in-del | -/G | | | intron-variant, upstream-variant-2KB | Inppl1, LOC102639173 | Mm_Celera | 7:101835442 | CACCAAATGCCCACA[-/G]CCCCATCCCAAGAGT | 16332 |
rs217632062 | snp | C/T | | | upstream-variant-2KB, downstream-variant-500B, intron-variant | Inppl1, LOC102639173 | Mm_Celera | 7:101839244 | AATAGTTTCTTTGGC[C/T]TCATCAGTAGGATAC | 16332 |
rs217827501 | snp | C/T | | | intron-variant | Inppl1 | Mm_Celera | 7:101824838 | TGCTCTTCCGAAGGT[C/T]CGGAGTTCAAATCCC | 16332 |
rs217857378 | snp | A/C | | | intron-variant | Inppl1 | Mm_Celera | 7:101823782 | TGTCCCCCAAAAGGC[A/C]CATTATCCAGCTACA | 16332 |
rs218206557 | snp | G/T | | | intron-variant | Inppl1 | Mm_Celera | 7:101833157 | GGAGTCAAAGAACTG[G/T]CAAGGAAGGGATTTT | 16332 |
rs218319298 | snp | A/T | | | intron-variant | Inppl1 | Mm_Celera | 7:101825128 | GTTGGGAAAGTGGTG[A/T]TCTTTAGGATGTCCA | 16332 |
rs218321532 | snp | A/G | | | missense, nc-transcript-variant | Inppl1 | Mm_Celera | 7:101824540 | CTCCTTCCTGCTCAG[A/G]TGTCCCTTCTGACTT | 16332 |