SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs6168664 | snp | A/T | 0.32 | 0.24 | intron-variant | Fam188a | Mm_Celera | 2:12365175 | GCTCATATCTAAGCC[A/T]CTGCGACATCCTACT | 66960 |
rs6170503 | snp | C/T | 0.5 | 0 | intron-variant | Fam188a | Mm_Celera | 2:12365535 | GAGGTCTTACCTGCT[C/T]NTGGACCACCTTCCT | 66960 |
rs6170506 | snp | C/G | 0.5 | 0 | intron-variant | Fam188a | Mm_Celera | 2:12365536 | AGGTCTTACCTGCTN[C/G]TGGACCACCTTCCTC | 66960 |
rs6204593 | snp | C/G | 0.5 | 0 | downstream-variant-500B | Fam188a | Mm_Celera | 2:12346974 | gatctttactttcaa[C/G]tgtgaagtgctaagt | 66960 |
rs6204626 | snp | G/T | 0.5 | 0 | downstream-variant-500B | Fam188a | Mm_Celera | 2:12346996 | gtgctaagtttcggg[G/T]gtgcagtaccatgcc | 66960 |
rs6204675 | snp | C/G | 0.5 | 0 | downstream-variant-500B | Fam188a | Mm_Celera | 2:12347021 | catgcccaatttaca[C/G]tgtantgaagactga | 66960 |
rs6204692 | snp | C/T | 0.5 | 0 | downstream-variant-500B | Fam188a | Mm_Celera | 2:12347026 | ccaatttacantgta[C/T]tgaagactgancaca | 66960 |
rs6204718 | snp | A/T | 0.5 | 0 | downstream-variant-500B | Fam188a | Mm_Celera | 2:12347037 | tgtantgaagactga[A/T]cacagggcttcatgt | 66960 |
rs6217524 | snp | C/T | 0.456747 | 0.140554 | downstream-variant-500B | Fam188a | Mm_Celera | 2:12347143 | TACAAAGCATTATGC[C/T]GCACCATTTCACACA | 66960 |
rs6218047 | snp | C/T | 0.207612 | 0.24638 | downstream-variant-500B | Fam188a | Mm_Celera | 2:12347223 | AGAAAGCATTATGAG[C/T]ACTTGGTGATACTGA | 66960 |
rs6218087 | snp | A/T | 0.5 | 0 | downstream-variant-500B | Fam188a | Mm_Celera | 2:12347244 | GTGATACTGAGTCAC[A/T]AATGTAAAAGTGCAA | 66960 |
rs6218650 | snp | G/T | 0.5 | 0 | utr-variant-3-prime, nc-transcript-variant | Fam188a | Mm_Celera | 2:12347337 | TATGCTAATGTAACA[G/T]TAGAGATTCTCATGC | 66960 |
rs6219757 | snp | A/C | 0.5 | 0 | utr-variant-3-prime, nc-transcript-variant | Fam188a | Mm_Celera | 2:12347550 | tttttattttatttt[A/C]ttttttGGTAAACAT | 66960 |
rs6376848 | snp | C/T | 0.5 | 0 | intron-variant | Fam188a | Mm_Celera | 2:12368835 | gtgtgtgcatgtttg[C/T]gcacatacatacaGA | 66960 |
rs6389884 | snp | A/C | 0.5 | 0 | intron-variant | Fam188a | Mm_Celera | 2:12368930 | gatttccacatcaaa[A/C]gcaatggaattggac | 66960 |
rs6389929 | snp | A/G | 0.5 | 0 | intron-variant | Fam188a | Mm_Celera | 2:12368957 | ggactcgtagttcac[A/G]tcagatntgagcatc | 66960 |
rs6389946 | snp | A/C | 0.5 | 0 | intron-variant | Fam188a | Mm_Celera | 2:12368964 | tagttcacntcagat[A/C]tgagcatcatttcaa | 66960 |
rs6390350 | snp | G/T | 0.5 | 0 | intron-variant | Fam188a | Mm_Celera | 2:12368993 | aaaatggatcacaac[G/T]tcaacgtangaaaaa | 66960 |
rs6390369 | snp | A/C | 0.5 | 0 | intron-variant | Fam188a | Mm_Celera | 2:12369002 | cacaacntcaacgta[A/C]gaaaaagaactctan | 66960 |
rs6390386 | snp | A/T | 0.5 | 0 | intron-variant | Fam188a | Mm_Celera | 2:12369017 | ngaaaaagaactcta[A/T]aactacagaagaaaa | 66960 |
rs6390947 | snp | A/T | 0.5 | 0 | intron-variant | Fam188a | Mm_Celera | 2:12369123 | AGCAACAGCCAAATT[A/T]AAAACCCatacttgt | 66960 |
rs6391517 | snp | C/T | 0.5 | 0 | intron-variant | Fam188a | Mm_Celera | 2:12369211 | aagaaaacaaaaatc[C/T]aatttaaaaagtggg | 66960 |
rs13471056 | snp | C/G | | | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | Fam188a | Mm_Celera | 2:12419229 | AGTGACCAAAGAGCT[C/G]CTGGAGCTGGTGTGG | 66960 |
rs27146039 | snp | A/C | 0.132653 | 0.220748 | upstream-variant-2KB | Fam188a | Mm_Celera | 2:12421388 | TCCTTACAATTGCAG[A/C]GAGTTATTTACTTTT | 66960 |
rs27146040 | snp | C/T | 0.152778 | 0.230321 | upstream-variant-2KB | Fam188a | Mm_Celera | 2:12420411 | TAAAAGGATCCAGGT[C/T]CTTTCTGGCATATGG | 66960 |
rs27146041 | snp | A/G | 0.32 | 0.24 | upstream-variant-2KB | Fam188a | Mm_Celera | 2:12419817 | TATACCCTTGAGTTG[A/G]AAGTTGCCTTCCTCA | 66960 |
rs27146042 | snp | C/G | 0.391111 | 0.206368 | utr-variant-5-prime, nc-transcript-variant | Fam188a | Mm_Celera | 2:12419290 | GGTCTTTGCTTCTCG[C/G]ACTCCGGTCCCGGAA | 66960 |
rs27146043 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Fam188a | Mm_Celera | 2:12418869 | AAAGAGTGCGGATAC[G/T]AGAGGGACTGAAGCC | 66960 |
rs27146044 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fam188a | Mm_Celera | 2:12418867 | GGAAAGAGTGCGGAT[A/G]CTAGAGGGACTGAAG | 66960 |
rs27146045 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Fam188a | Mm_Celera | 2:12418687 | CTGAGCGCAGAGTCC[C/T]GAAAGTGGTCAGAGC | 66960 |
rs27146046 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Fam188a | Mm_Celera | 2:12418661 | ATTGGAATCAAGTCC[A/G]GGATCTAGAACTGAG | 66960 |
rs27146047 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Fam188a | Mm_Celera | 2:12418200 | ACTCGAAGGCTGGAG[A/G]TGTAATGATCTTAAC | 66960 |
rs27146048 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Fam188a | Mm_Celera | 2:12418107 | ATGAAACTGCTTTCC[A/C]GTATTACTCACCTAG | 66960 |
rs27146049 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Fam188a | Mm_Celera | 2:12417635 | CAACTATGTGTTATT[C/G]GGTTGGCTTATTTTA | 66960 |
rs27146050 | snp | A/G | 0.124444 | 0.216185 | intron-variant, upstream-variant-2KB | Fam188a | Mm_Celera | 2:12416860 | TTTCTTCAGATACCT[A/G]CATGGCTCCCTCCAG | 66960 |
rs27146051 | snp | G/T | 0.124444 | 0.216185 | intron-variant, upstream-variant-2KB | Fam188a | Mm_Celera | 2:12416812 | ATTAGACACCAAGAT[G/T]TGTACAGGGGTGAGG | 66960 |
rs27146052 | snp | A/C | 0.124444 | 0.216185 | intron-variant, upstream-variant-2KB | Fam188a | Mm_Celera | 2:12416784 | GCCACACTGAACCAA[A/C]AGTCCAAGGAACATT | 66960 |
rs27146053 | snp | A/C | 0.444444 | 0.157135 | intron-variant, upstream-variant-2KB | Fam188a | Mm_Celera | 2:12416337 | AACCTAGAAAGAGCA[A/C]AGTCCCTGACAGGGA | 66960 |
rs27146054 | snp | A/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | Fam188a | Mm_Celera | 2:12416083 | AAGATGGCCTGCCTC[A/T]TCACAAAACAAAAAA | 66960 |
rs27146055 | snp | A/T | 0.444444 | 0.157135 | intron-variant, upstream-variant-2KB | Fam188a | Mm_Celera | 2:12415610 | ACAGCATAACATCAT[A/T]TGGCAGACATTTAAA | 66960 |
rs27146056 | snp | A/T | 0.5 | 0 | intron-variant | Fam188a | Mm_Celera | 2:12405270 | TCTGATAGTTTATTC[A/T]GCAAACTTTCAGTGT | 66960 |
rs27146057 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Fam188a | Mm_Celera | 2:12404300 | GGAAAACCCATATGA[C/T]CAGAAGACTGGAAAT | 66960 |
rs27146058 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Fam188a | Mm_Celera | 2:12403839 | CCTTTTGTAAAAATG[C/G]ACTGTCTTACACTAA | 66960 |
rs27146059 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Fam188a | Mm_Celera | 2:12403169 | ATGGATAGTGATACA[C/T]AACACACACAATCAA | 66960 |
rs27146060 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Fam188a | Mm_Celera | 2:12403111 | ACAGTGAACACAGAC[A/G]TTTCAGCTCAGGGGA | 66960 |
rs27146061 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Fam188a | Mm_Celera | 2:12402961 | AAATGAATTCTTTTC[A/G]AAAGGCAATATTTTA | 66960 |
rs27146062 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fam188a | Mm_Celera | 2:12402674 | CCAACGTGTTAGCAC[A/G]GAAATGCACCACCAC | 66960 |
rs27146063 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Fam188a | Mm_Celera | 2:12402664 | CTAGAGCTTGCCAAC[A/G]TGTTAGCACAGAAAT | 66960 |
rs27146064 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fam188a | Mm_Celera | 2:12402659 | TCCTCCTAGAGCTTG[C/T]CAACGTGTTAGCACA | 66960 |
rs27146065 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fam188a | Mm_Celera | 2:12402553 | TTTTAAAATGAGGCA[C/T]TAAGTAAACTAGAAA | 66960 |
rs27146066 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Fam188a | Mm_Celera | 2:12402337 | GTCAGAGATGGTGGG[A/G]AATAAAGACAAGAGG | 66960 |
rs27146067 | snp | A/T | 0.132653 | 0.220748 | intron-variant | Fam188a | Mm_Celera | 2:12402267 | ACATAAAGAGAATAC[A/T]TTCAAGAGGCTGGCA | 66960 |
rs27146068 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Fam188a | Mm_Celera | 2:12401399 | ACATTGTCATGTGTC[C/T]TGAATTTAAAATAAT | 66960 |
rs27146069 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Fam188a | Mm_Celera | 2:12401173 | AAGCAATCAAAACAT[C/T]CCCTATTTCTTATTC | 66960 |
rs27146070 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fam188a | Mm_Celera | 2:12400429 | TTATTTAGACCACAG[A/G]CTGGACCTCTTCAGA | 66960 |
rs27146071 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Fam188a | Mm_Celera | 2:12400318 | CTGACAGCTCCTACT[A/C]TACATAACCCAGTCT | 66960 |
rs27146072 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Fam188a | Mm_Celera | 2:12400291 | TTTAGCCATGGAAAA[C/G]AAAAACTACTGCTGA | 66960 |
rs27146073 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Fam188a | Mm_Celera | 2:12399671 | AATATGAGACACTCT[A/C]TGAGAAACTAGCATA | 66960 |
rs27146074 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Fam188a | Mm_Celera | 2:12399408 | ACATTCCAAGTGTGA[G/T]TGCAAGGCCACAAGC | 66960 |
rs27146075 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fam188a | Mm_Celera | 2:12399159 | CCTGTCAACAAACTT[A/G]AGTCATAGCTTCTAT | 66960 |
rs27146076 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Fam188a | Mm_Celera | 2:12399125 | AATGGTCCTTACTAC[C/G]CAGAATTTGCTCTTG | 66960 |
rs27146077 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fam188a | Mm_Celera | 2:12399068 | TTGCTTCTCCTACTG[C/T]TTGTAAAACTCTTCT | 66960 |
rs27146078 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Fam188a | Mm_Celera | 2:12398827 | TTCAGGCATCTTCTA[A/G]CCACACAATAAGATC | 66960 |
rs27146079 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Fam188a | Mm_Celera | 2:12398740 | TTTCAGCTTCTACTA[C/T]AATACTACTTCAGTA | 66960 |
rs27146080 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Fam188a | Mm_Celera | 2:12397680 | TTTGAGATGGTAAGA[A/T]GTAGCCCCCAAAGAT | 66960 |
rs27146081 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Fam188a | Mm_Celera | 2:12397654 | CACTGTTCAAATGAC[A/C]CAGACTTGTATTTGA | 66960 |
rs27146082 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Fam188a | Mm_Celera | 2:12397311 | GTCATGTGTAAACAA[A/C]CTGAAATTGGATGTC | 66960 |
rs27146083 | snp | A/G | 0.32 | 0.24 | intron-variant | Fam188a | Mm_Celera | 2:12397044 | TAGACACGTGCAAAA[A/G]GAAGGACTTGTGTGA | 66960 |
rs27146084 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Fam188a | Mm_Celera | 2:12396086 | AGCACTTACCTTAGC[A/G]TCCACATAATGTAGA | 66960 |
rs27146085 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fam188a | Mm_Celera | 2:12395875 | TCTGAATAAGTACCC[A/G]TATGTTACACCCACT | 66960 |
rs27146086 | snp | A/C | 0.32 | 0.24 | intron-variant | Fam188a | Mm_Celera | 2:12395786 | GTGATAATAAACGCA[A/C]GGATCTTGTAAGAAC | 66960 |
rs27146087 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Fam188a | Mm_Celera | 2:12395711 | CTGACTGAATTCAGG[A/T]GAGTGGATGCAGTCT | 66960 |
rs27146088 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Fam188a | Mm_Celera | 2:12395655 | TCCTGGCCAGTGTGC[A/G]TCCCTTGATGTCTGC | 66960 |
rs27146089 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fam188a | Mm_Celera | 2:12395630 | CAACAGCTGTCTGAG[C/T]GAGCGAATGTCCTGG | 66960 |
rs27146090 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Fam188a | Mm_Celera | 2:12395606 | GAAGGAGCTTTCCTC[A/C]TAGCCGCACAACAGC | 66960 |
rs27146091 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fam188a | Mm_Celera | 2:12394859 | GCTGGCCAGTTCTCA[C/T]GGGCTTTTACATCTA | 66960 |
rs27146092 | snp | C/T | 0.32 | 0.24 | intron-variant | Fam188a | Mm_Celera | 2:12394740 | CTTCTCTAGTTCTCC[C/T]GATTACAGCAGATTT | 66960 |
rs27146093 | snp | C/G | 0.152778 | 0.230321 | intron-variant | Fam188a | Mm_Celera | 2:12394646 | GTAATGAATAAAAGA[C/G]TTAACAGTTGTGGGC | 66960 |
rs27146094 | snp | A/G | 0.32 | 0.24 | intron-variant | Fam188a | Mm_Celera | 2:12394592 | GGATAACCTGAGAGA[A/G]ACTGTAGGGTACACA | 66960 |
rs27146095 | snp | A/T | 0.142012 | 0.225474 | intron-variant | Fam188a | Mm_Celera | 2:12394482 | AAGCTTATATAAGTG[A/T]TGAACAAATTCTGTA | 66960 |
rs27146096 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fam188a | Mm_Celera | 2:12394457 | ATGAATTTGCATATA[C/T]GAGGAACCAAAGCTT | 66960 |
rs27146097 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fam188a | Mm_Celera | 2:12394454 | TGAATGAATTTGCAT[A/G]TACGAGGAACCAAAG | 66960 |
rs27146098 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Fam188a | Mm_Celera | 2:12394222 | AAAATTATGTACGGA[C/T]TTTATTTTATGCTTA | 66960 |
rs27146099 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fam188a | Mm_Celera | 2:12394010 | GCTCTTCCTTTGAGT[C/T]CTTGCAGACATGACA | 66960 |
rs27146100 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Fam188a | Mm_Celera | 2:12393963 | ATTTCAGCACATATC[A/G]TATCATCTATGTGCA | 66960 |
rs27146101 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Fam188a | Mm_Celera | 2:12393925 | TCCTCAGCATGTCTA[G/T]GGTCCTTATTTCAAC | 66960 |
rs27146102 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Fam188a | Mm_Celera | 2:12393605 | GCTGCCGCATTCCCT[C/T]ACCAGTGCTCATCAC | 66960 |
rs27146103 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Fam188a | Mm_Celera | 2:12393483 | CTCCAGTACGGCTAC[A/C]CACGGACAGCATCCT | 66960 |
rs27146104 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Fam188a | Mm_Celera | 2:12393029 | ATGTTCTATACAGAA[C/T]AAGCAGAGGCTTTAC | 66960 |
rs27146105 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fam188a | Mm_Celera | 2:12392968 | CCCTCACCTCTAAAA[C/T]GAAAAGTCCTACAAG | 66960 |
rs27146106 | snp | A/G | 0.32 | 0.24 | intron-variant | Fam188a | Mm_Celera | 2:12392578 | TTGCTCCTTAGAGCA[A/G]CGGACTCACATCTCT | 66960 |
rs27146107 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fam188a | Mm_Celera | 2:12392306 | AATGCTCAAGGCAAA[A/G]GATACACATGATGGT | 66960 |
rs27146108 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Fam188a | Mm_Celera | 2:12392014 | GTTGTTGGCATGGAG[C/T]GGATGGAAGTAAGGG | 66960 |
rs27146109 | snp | A/T | 0.32 | 0.24 | intron-variant | Fam188a | Mm_Celera | 2:12391686 | ATTGATATTTTAGGG[A/T]CAAAGTTGCCATAAA | 66960 |
rs27146110 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Fam188a | Mm_Celera | 2:12391508 | AGCACAGCTGCAGGC[C/T]TACACGTGAGCAAAG | 66960 |
rs27146111 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Fam188a | Mm_Celera | 2:12391477 | AGATGATGAGCAGAG[A/G]CAGTTCCCAGAGGAC | 66960 |
rs27146112 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Fam188a | Mm_Celera | 2:12391007 | CCACTTATCTTTAAG[C/T]TAATGACCATCAACT | 66960 |
rs27146113 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Fam188a | Mm_Celera | 2:12390230 | ACCTAAGCCAGATAC[C/T]TGAGCGTGGTTCTTG | 66960 |
rs27146114 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Fam188a | Mm_Celera | 2:12389748 | CAATTTTATGACTAT[C/G]TTGCCATTGCCTATA | 66960 |
rs27146115 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Fam188a | Mm_Celera | 2:12389694 | CATTGGATTTTCTTT[A/G]AAAGTCTCAGTCTTT | 66960 |