SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs13471432 | snp | G/T | 0.165289 | 0.235211 | utr-variant-3-prime | Socs6 | GRCm38.p3 | 18:88868859 | ATGCATTAAAGCACA[G/T]TTCATGTGTATTCAA | 54607 |
rs13471435 | snp | C/T | | | utr-variant-3-prime | Socs6 | Mm_Celera | 18:88869043 | GCCTTGCAGACACTT[C/T]CCCACCCTTGAACAA | 54607 |
rs29538156 | snp | A/C | 0.375 | 0.216506 | utr-variant-3-prime | Socs6 | Mm_Celera | 18:88868446 | AGAGCTTTTAAGTTA[A/C]GCCAATTTGTACCCG | 54607 |
rs29548008 | snp | G/T | 0.444444 | 0.157135 | upstream-variant-2KB | Socs6 | Mm_Celera | 18:88895213 | ATTCTCAGTATTGAC[G/T]TGAATGGATTATTGA | 54607 |
rs29580024 | snp | C/T | 0.375 | 0.216506 | intron-variant | Socs6 | Mm_Celera | 18:88881979 | GAAATCAACTTTTTA[C/T]TTTTGGTTCACTCTC | 54607 |
rs29620640 | snp | C/T | 0.375 | 0.216506 | intron-variant | Socs6 | Mm_Celera | 18:88880443 | ATGAAATACAGTTGC[C/T]TGTATTTTCTACAAA | 54607 |
rs29669547 | snp | A/C | 0.244898 | 0.249948 | intron-variant | Socs6 | Mm_Celera | 18:88881502 | GGCCATGTAAATGCA[A/C]CAGTTTCAAGAAAAG | 54607 |
rs29679423 | snp | C/T | 0.401235 | 0.199068 | intron-variant | Socs6 | Mm_Celera | 18:88879601 | AAAAATAAAAGAAAG[C/T]GATGCAGTTTATAAA | 54607 |
rs29718461 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Socs6 | Mm_Celera | 18:88870928 | TATTTTCTGGGGGGG[A/G]AAAAAAGGCCATTAA | 54607 |
rs29723045 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Socs6 | Mm_Celera | 18:88883601 | AAAAAAACCAACCCC[C/T]CCCCAAAAAAAGTGA | 54607 |
rs29767277 | snp | G/T | 0.48 | 0.0979796 | intron-variant | Socs6 | Mm_Celera | 18:88892535 | GGCAAAAATTAGCAG[G/T]GTTTTCTCCAAGCAG | 54607 |
rs29861435 | snp | C/T | 0.401235 | 0.199068 | utr-variant-3-prime | Socs6 | Mm_Celera | 18:88869177 | GTGCAAGAAACAGGG[C/T]TCCAAATCTCTCAGT | 54607 |
rs29921992 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Socs6 | Mm_Celera | 18:88881143 | TAGAACTCTCAGCTC[C/T]TCCTGCGCCATGCCT | 54607 |
rs29935627 | snp | C/T | 0.444444 | 0.157135 | downstream-variant-500B, utr-variant-3-prime | Socs6 | Mm_Celera | 18:88867531 | AATAGTGAATGCTTA[C/T]ACTATCTCCATATAA | 54607 |
rs29936495 | snp | A/G | 0.207612 | 0.24638 | intron-variant | Socs6 | Mm_Celera | 18:88882227 | ACTCCAATTAATAAT[A/G]TCTGTTCCACATCAC | 54607 |
rs29959574 | snp | G/T | 0.5 | 0 | intron-variant | Socs6 | Mm_Celera | 18:88884919 | AATATATCTATTCCT[G/T]CATCCTGCATCTGGG | 54607 |
rs29972917 | snp | A/C | 0.5 | 0 | intron-variant | Socs6 | Mm_Celera | 18:88886057 | ATATGAGGGGACCTG[A/C]AGATAAGTGGGTCTA | 54607 |
rs30024962 | snp | G/T | 0.48 | 0.0979796 | intron-variant | Socs6 | Mm_Celera | 18:88881154 | GCTCCTCCTGCGCCA[G/T]GCCTGCCTGGATGCT | 54607 |
rs30026144 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Socs6 | Mm_Celera | 18:88893028 | AGTCCAGAAGCCAAG[C/T]CCTCAAAGAAACAAG | 54607 |
rs30059028 | snp | C/T | 0.5 | 0 | intron-variant | Socs6 | Mm_Celera | 18:88879872 | AGAATAATACCTAAG[C/T]CAAACACAAGAGACC | 54607 |
rs30079766 | snp | A/G | 0.5 | 0 | downstream-variant-500B | Socs6 | Mm_Celera | 18:88864732 | CAGGCAGACAGACAG[A/G]CAGGCAGGCAGGCAG | 54607 |
rs30179780 | snp | C/T | 0.375 | 0.216506 | intron-variant | Socs6 | Mm_Celera | 18:88882037 | TTCCTCACATCTAAA[C/T]ACTCCATCTTCTATC | 54607 |
rs30214392 | snp | A/T | 0.48 | 0.0979796 | intron-variant | Socs6 | Mm_Celera | 18:88881144 | AGAACTCTCAGCTCC[A/T]CCTGCGCCATGCCTG | 54607 |
rs30220182 | snp | A/T | 0.375 | 0.216506 | upstream-variant-2KB | Socs6 | Mm_Celera | 18:88894550 | CTTTCTCTGGCTTGG[A/T]CTTAAGAAAACTAAT | 54607 |
rs30223641 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Socs6 | Mm_Celera | 18:88889514 | GCTTCAGGGTGGCAC[C/T]GACACCCTTGGGGTC | 54607 |
rs30301700 | snp | A/G | 0.290657 | 0.246672 | downstream-variant-500B | Socs6 | Mm_Celera | 18:88864972 | TCACTCCATTATATT[A/G]GCCACTGAAGTATAG | 54607 |
rs30301736 | snp | A/C | 0.48 | 0.0979796 | intron-variant | Socs6 | Mm_Celera | 18:88883605 | AAACCAACCCCCCCC[A/C]AAAAAAAGTGAGCAT | 54607 |
rs33851562 | snp | A/T | 0.387812 | 0.208586 | intron-variant | Socs6 | Mm_Celera | 18:88874366 | TTATCAAATTCATAT[A/T]TGCTTTAGCCAAGTA | 54607 |
rs36244827 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Socs6 | Mm_Celera | 18:88884742 | ACCAGAAGAGGTCAT[G/T]GTGGGAAACTCTGAC | 54607 |
rs36267724 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Socs6 | Mm_Celera | 18:88871348 | CCCAAAAATCTTATA[C/G]CTTTCCACTGCAGCT | 54607 |
rs36273187 | snp | G/T | 0.244898 | 0.249948 | intron-variant | Socs6 | Mm_Celera | 18:88888326 | CTCCTGAGTAAATAG[G/T]ACCTAAAATTCTATA | 54607 |
rs36295133 | snp | G/T | 0.32 | 0.24 | intron-variant | Socs6 | Mm_Celera | 18:88891230 | TGCTCCAGAATAACT[G/T]CTTTCCACACTGACA | 54607 |
rs36351135 | snp | A/C | 0.231111 | 0.249285 | downstream-variant-500B, utr-variant-3-prime | Socs6 | Mm_Celera | 18:88867671 | ATGTTGGCACTGAGC[A/C]TTTTCCTGCAATATC | 54607 |
rs36373056 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Socs6 | Mm_Celera | 18:88875285 | TCTCACTTGCCAAAG[C/T]TGAACAGTGTAATAC | 54607 |
rs36401973 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Socs6 | Mm_Celera | 18:88871873 | CCCAGAAAGCAGACT[C/T]AGTAGCTGATAGTCA | 54607 |
rs36408948 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Socs6 | Mm_Celera | 18:88880088 | TCTCTTCCACTTTGT[A/G]GATTCTGGGTATAGA | 54607 |
rs36411563 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Socs6 | Mm_Celera | 18:88872374 | TACTTGCCACTAAAC[C/T]TGATTCCTGCTACTT | 54607 |
rs36427986 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Socs6 | Mm_Celera | 18:88879904 | AGAGGTGGGTATCCC[A/G]AGGTTCCAAAAACCC | 54607 |
rs36439223 | snp | A/C | 0.124444 | 0.216185 | synonymous-codon | Socs6 | GRCm38.p3 | 18:88869299 | GCACAGGTACTGCAG[A/C]GAGCGCACCTGCATG | 54607 |
rs36491776 | snp | A/C | 0.32 | 0.24 | intron-variant | Socs6 | Mm_Celera | 18:88884476 | AGGGCTATGATAAGA[A/C]TGTAAAGGGAAAAAA | 54607 |
rs36511561 | snp | A/T | 0.142012 | 0.225474 | intron-variant | Socs6 | Mm_Celera | 18:88885510 | TTCAATGCACTGAAC[A/T]ATAATAGTAACAACA | 54607 |
rs36519486 | snp | C/T | 0.231111 | 0.249285 | utr-variant-3-prime | Socs6 | Mm_Celera | 18:88865321 | TTTGGATAATTCATT[C/T]TGTGGTGTTCTCAGT | 54607 |
rs36530974 | snp | C/T | 0.32 | 0.24 | intron-variant | Socs6 | Mm_Celera | 18:88889818 | GCTATGACCTGTGAA[C/T]CCTTCTATATACACA | 54607 |
rs36596022 | snp | C/G | 0.391111 | 0.206368 | utr-variant-3-prime | Socs6 | Mm_Celera | 18:88866103 | CTTTCTAATTTTTCA[C/G]AGTATTGCACCATGT | 54607 |
rs36605260 | snp | A/T | 0.46281 | 0.131194 | intron-variant | Socs6 | Mm_Celera | 18:88889164 | TGCACAAGTGAAGTA[A/T]TGCACAACAAAATAG | 54607 |
rs36647373 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Socs6 | Mm_Celera | 18:88880220 | ATCACTCAGGATCAT[A/C]TAAATAGCTCTATTC | 54607 |
rs36681764 | snp | A/T | 0.375 | 0.216506 | intron-variant | Socs6 | Mm_Celera | 18:88879778 | TGAACATACACACAC[A/T]CTCTGAGTAAATGAC | 54607 |
rs36708501 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Socs6 | Mm_Celera | 18:88872271 | TTGAAAAATTTGTAT[A/G]ACGGTTCAAGGGAAA | 54607 |
rs36732903 | snp | C/T | 0.408163 | 0.193609 | utr-variant-3-prime | Socs6 | Mm_Celera | 18:88866323 | TCTGCTTGCTTTTGT[C/T]TTGCCTTAATGTAGG | 54607 |
rs36790928 | snp | A/G | 0.32 | 0.24 | downstream-variant-500B, utr-variant-3-prime | Socs6 | Mm_Celera | 18:88867711 | ACCCTAGAAAAAGAG[A/G]AAAAATGTAAAGCTA | 54607 |
rs36791161 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Socs6 | Mm_Celera | 18:88881682 | TACTGATATGCACCA[C/T]GGTTTACTGGTCTTA | 54607 |
rs36838166 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Socs6 | Mm_Celera | 18:88871761 | CATACACTGTTTCTG[A/G]AAGATATTGTAAAAA | 54607 |
rs36843652 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Socs6 | Mm_Celera | 18:88880372 | GTTTCTGACTCTGTC[C/G]CTTTTGTGCTTTTAT | 54607 |
rs36855911 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Socs6 | Mm_Celera | 18:88874730 | AAGCAATGTCTTATT[A/G]CATAGGCTAAATACT | 54607 |
rs36865258 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Socs6 | Mm_Celera | 18:88889645 | AATGGGATAATCGTT[A/G]CAACTGTCTTCAGAA | 54607 |
rs36879651 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Socs6 | Mm_Celera | 18:88882457 | CAGTTGTCTTTCACC[A/G]CCACAGCAAGCAGCC | 54607 |
rs36888151 | snp | A/G | 0.32 | 0.24 | intron-variant | Socs6 | Mm_Celera | 18:88888780 | ATTGAACTCTTTCAA[A/G]TCTGAAATTACAACA | 54607 |
rs36890731 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Socs6 | Mm_Celera | 18:88887395 | CTTAGACTACCCTTA[A/G]ATGCAGCACCCAGTG | 54607 |
rs36921422 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Socs6 | Mm_Celera | 18:88876644 | ATGAGGAGGCTTGCG[A/T]GTCCTTTCCCTCCCA | 54607 |
rs36943468 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Socs6 | Mm_Celera | 18:88877037 | GAAAAGACTGGAAAT[A/G]AAATGATAAATGTAA | 54607 |
rs36990629 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Socs6 | Mm_Celera | 18:88890228 | TAAAATTCAATCTAC[A/G]TTTGTATCCCTGTGA | 54607 |
rs37084619 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Socs6 | Mm_Celera | 18:88871813 | GAGCACAAGACACTT[C/T]AAACATGAAGCTATG | 54607 |
rs37184304 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Socs6 | Mm_Celera | 18:88880028 | AGTACTGTTGGGACT[A/G]TGTGCACATTTGTAG | 54607 |
rs37235040 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Socs6 | Mm_Celera | 18:88885436 | CTGGGTAGAAGTAAT[A/G]TAGCAGACTGATGCT | 54607 |
rs37251318 | snp | A/G | 0.391111 | 0.206368 | downstream-variant-500B | Socs6 | Mm_Celera | 18:88864973 | CACTCCATTATATTG[A/G]CCACTGAAGTATAGC | 54607 |
rs37265219 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Socs6 | Mm_Celera | 18:88888121 | ATATGCTGGATTCTG[A/G]ACCTGCCATCCTCTC | 54607 |
rs37274118 | snp | A/C | 0.124444 | 0.216185 | utr-variant-3-prime | Socs6 | GRCm38.p3 | 18:88868803 | GGGCCATTTAACATC[A/C]TAGCAATTTATATTT | 54607 |
rs37314350 | snp | C/T | 0.391111 | 0.206368 | utr-variant-3-prime | Socs6 | Mm_Celera | 18:88867142 | CAGAATAGCACAAAT[C/T]GATTATTAGAAATAT | 54607 |
rs37328732 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Socs6 | Mm_Celera | 18:88879292 | TTTGTCTCAAGTACT[A/G]TGGGCAACAGACACT | 54607 |
rs37333450 | snp | A/G | 0.391111 | 0.206368 | utr-variant-3-prime | Socs6 | GRCm38.p3 | 18:88868090 | CACATAATGTATCAC[A/G]ATTTTTAATTATTTA | 54607 |
rs37343984 | snp | A/G | 0.197531 | 0.244432 | utr-variant-3-prime | Socs6 | Mm_Celera | 18:88866955 | GCTACAAAAACACAA[A/G]AATATTGGCAATATT | 54607 |
rs37386672 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Socs6 | Mm_Celera | 18:88872654 | GTGAATTAAGGAGTG[C/T]TGATACAAGGACTAG | 54607 |
rs37455818 | snp | A/T | 0.132653 | 0.220748 | intron-variant | Socs6 | Mm_Celera | 18:88886605 | AGATATAGAATGTGG[A/T]AAAGTGCTTACTTGA | 54607 |
rs37458044 | snp | C/T | 0.165289 | 0.235211 | intron-variant | Socs6 | Mm_Celera | 18:88889189 | AAATAGTACACCCAC[C/T]AGTGAGAACTCATCT | 54607 |
rs37495120 | snp | C/G | 0.297521 | 0.245442 | intron-variant | Socs6 | Mm_Celera | 18:88889382 | TCTTTTTCTCTAATA[C/G]GGGCCTCACATACTT | 54607 |
rs37506773 | snp | C/T | 0.124444 | 0.216185 | utr-variant-3-prime | Socs6 | Mm_Celera | 18:88868102 | CACAATTTTTAATTA[C/T]TTAGCTGATGTCATT | 54607 |
rs37520643 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Socs6 | Mm_Celera | 18:88879629 | AAATAGCCATTGTAG[A/C]AATCATGTAAGCCTA | 54607 |
rs37553943 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Socs6 | Mm_Celera | 18:88876071 | TCTGAAAATTTAGCT[A/G]CAAGCAGTGGTTAGA | 54607 |
rs37556792 | snp | A/C | 0.391111 | 0.206368 | downstream-variant-500B, utr-variant-3-prime | Socs6 | Mm_Celera | 18:88867494 | GCACACAAGCCTACA[A/C]TTCTCCAATAGTTCT | 54607 |
rs37603732 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Socs6 | Mm_Celera | 18:88879043 | TAGAATGTTGAAGAT[C/T]CCTACACTAAAAACC | 54607 |
rs37605098 | snp | C/T | 0.46281 | 0.131194 | intron-variant | Socs6 | Mm_Celera | 18:88872107 | GAGATTACTCTAAAA[C/T]TTTTTTAAAGAATAT | 54607 |
rs37671161 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Socs6 | Mm_Celera | 18:88882438 | ATCCTGCTTTGTACT[C/T]TGCCAGTTGTCTTTC | 54607 |
rs37711284 | snp | C/G | 0.152778 | 0.230321 | intron-variant | Socs6 | Mm_Celera | 18:88889561 | GCTTGCCACTGAGGT[C/G]TTCAGTGACATCTCA | 54607 |
rs37722984 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Socs6 | Mm_Celera | 18:88883209 | AGTAACAAAGCCCTT[C/T]ATTTTGTACTCTACA | 54607 |
rs37730377 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Socs6 | Mm_Celera | 18:88888514 | ACTTACAGGCTCTTT[C/T]CATCTCTGCATCTTT | 54607 |
rs37778002 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Socs6 | Mm_Celera | 18:88887531 | AGAAGAAATGTCCCT[C/G]AGAAATGATCACAAC | 54607 |
rs37840131 | snp | A/G | 0.391111 | 0.206368 | synonymous-codon | Socs6 | GRCm38.p3 | 18:88869815 | TGGGCCCGAGAGGCC[A/G]CTGAAGTTCCTTTGG | 54607 |
rs37852564 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Socs6 | Mm_Celera | 18:88875421 | TTACTCTATATACCC[A/C]ACAATGACTTCAGCC | 54607 |
rs37868736 | snp | A/G | 0.124444 | 0.216185 | downstream-variant-500B | Socs6 | Mm_Celera | 18:88864764 | CAGGCATGCACAGGT[A/G]CAAACTTTTACAAAG | 54607 |
rs37886957 | snp | G/T | 0.32 | 0.24 | utr-variant-3-prime | Socs6 | Mm_Celera | 18:88867924 | ACTTTTAAAACCTGG[G/T]CTCATCATTCTCTAA | 54607 |
rs38008606 | snp | C/T | 0.124444 | 0.216185 | utr-variant-3-prime | Socs6 | Mm_Celera | 18:88868153 | TAGAATGGTCAAACA[C/T]AGCACACTGTAAAGA | 54607 |
rs38014768 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Socs6 | Mm_Celera | 18:88879697 | AAACCCTTGAGAATA[C/T]AGAACTTAAATCAAG | 54607 |
rs38030166 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Socs6 | Mm_Celera | 18:88889975 | TCCTATATTGGACAT[C/T]TTTAATAAGAATGTC | 54607 |
rs38062005 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Socs6 | Mm_Celera | 18:88885208 | TATAATTCACTGATA[C/T]ACTGTCATAATTGTC | 54607 |
rs38073210 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Socs6 | Mm_Celera | 18:88875209 | CCCACTTTCCTTATT[C/T]AGGACTTTCTGTAAC | 54607 |
rs38230947 | snp | A/G | 0.391111 | 0.206368 | utr-variant-3-prime | Socs6 | GRCm38.p3 | 18:88867967 | TAAGTAGAGGTGCCA[A/G]ACTACTTACAAATTA | 54607 |
rs38264580 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Socs6 | Mm_Celera | 18:88884254 | CTAATTCAAAGCAGC[A/G]TGAGTCGTTCCATGG | 54607 |
rs38431693 | snp | C/G | 0.391111 | 0.206368 | downstream-variant-500B | Socs6 | Mm_Celera | 18:88864690 | TTATGGATCTTCTGT[C/G]TATTTCAATCAATGT | 54607 |
rs38437356 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Socs6 | Mm_Celera | 18:88876882 | CAAATGCTGAAGGAC[A/G]TTCTGCTACCAAGAA | 54607 |
rs38577807 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Socs6 | Mm_Celera | 18:88884686 | AATCCTTACAATAAA[C/T]CAGTCAAATAAGTAT | 54607 |