SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs6207628 | snp | C/T | 0.5 | 0 | intron-variant | Faf2 | Mm_Celera | 13:54629077 | GCTTTGAAAAGGCTG[C/T]ACAGGGACGAGTCAC | 76577 |
rs6303671 | snp | A/T | 0.290657 | 0.246672 | intron-variant | Faf2 | Mm_Celera | 13:54628703 | TTATGCCAGCATATG[A/T]ATGAAGGCCACAGAT | 76577 |
rs6304704 | snp | A/G | 0.5 | 0 | intron-variant | Faf2 | Mm_Celera | 13:54628895 | TCGTGCACAGTAACC[A/G]GTTCCTTTCACTGAA | 76577 |
rs13462425 | snp | A/G | | | utr-variant-3-prime, upstream-variant-2KB | Faf2, LOC105245510 | Mm_Celera | 13:54663482 | CCAGTTCTGCCCCTC[A/G]TTCCCCTCTGAAGTG | 76577 |
rs13462426 | snp | A/G | | | utr-variant-3-prime | Faf2 | Mm_Celera | 13:54662300 | GTGGTGAAGCAGCAG[A/G]AGCCCTCCCCCCCCC | 76577 |
rs13462427 | snp | A/G | 0.32 | 0.24 | utr-variant-3-prime, upstream-variant-2KB | Faf2, LOC105245510 | Mm_Celera | 13:54663304 | TCTCTCCCTGGGTGA[A/G]CTGTGGACTTCACAT | 76577 |
rs13462428 | snp | A/G | 0.231111 | 0.249285 | utr-variant-3-prime | Faf2 | Mm_Celera | 13:54662389 | CCCACATGCCAGCGC[A/G]CACTGATAAGTATTC | 76577 |
rs13462429 | snp | G/T | 0.32 | 0.24 | utr-variant-3-prime | Faf2 | Mm_Celera | 13:54662343 | CTGTGACTGAATGTT[G/T]GGTAGTGGATATGTG | 76577 |
rs29226670 | snp | A/T | 0.32 | 0.24 | intron-variant | Faf2 | Mm_Celera | 13:54651338 | GAAGAAAATGAGGGG[A/T]GGAAGGAATTGGATG | 76577 |
rs29235305 | snp | A/G | 0.32 | 0.24 | utr-variant-3-prime | Faf2 | Mm_Celera | 13:54661823 | GGATTGTGACCCACA[A/G]AAGGCTGTGTGTGGG | 76577 |
rs45632226 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Faf2 | Mm_Celera | 13:54659792 | GGATACCAGGTTAGC[A/G]GACCACTTAAAATTA | 76577 |
rs45635103 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Faf2 | Mm_Celera | 13:54629060 | TCTATATGAAATTAA[C/T]TGCTTTGAAAAGGCT | 76577 |
rs45649593 | snp | A/G | 0.124444 | 0.216185 | utr-variant-3-prime | Faf2 | Mm_Celera | 13:54662074 | GCAAGTGTGATAACA[A/G]TGTCTAAGGATAGAC | 76577 |
rs45701171 | snp | A/G | 0.32 | 0.24 | intron-variant | Faf2 | Mm_Celera | 13:54623113 | TTATGCTAAGCCTTA[A/G]TGCCAGACACCGCCC | 76577 |
rs45705511 | snp | A/G | | | intron-variant, upstream-variant-2KB | Faf2 | Mm_Celera | 13:54644674 | TCCATAACTCAGGAA[A/G]TAATTTCCTGTGTCC | 76577 |
rs45706432 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Faf2 | Mm_Celera | 13:54640567 | GGGGAAGCCAGGCAT[C/T]TCTTTGGGCATGGCC | 76577 |
rs45773763 | snp | C/T | 0.231111 | 0.249285 | downstream-variant-500B, upstream-variant-2KB | Faf2, LOC105245510 | Mm_Celera | 13:54664448 | GGAAGAGTAGCGGTC[C/T]GTTCCTGTGTCCGAG | 76577 |
rs45809966 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Faf2 | Mm_Celera | 13:54652521 | ACATAGAACTTAATG[C/T]GAAGAAGGTGGACTG | 76577 |
rs45832566 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Faf2 | Mm_Celera | 13:54649932 | TAGCCTAAATAGTAG[C/T]TCCAGACCTTAGTAG | 76577 |
rs45973043 | snp | C/T | 0.32 | 0.24 | intron-variant | Faf2 | Mm_Celera | 13:54652301 | TGGGCACTTTAAAAG[C/T]CTTTGCTTCATGTTG | 76577 |
rs46039856 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Faf2 | Mm_Celera | 13:54633018 | GAAGCCTCAGCAAGC[C/T]AATTGGAGCACAAAG | 76577 |
rs46101899 | snp | C/T | 0.124444 | 0.216185 | utr-variant-3-prime | Faf2 | Mm_Celera | 13:54661537 | CCGGAACAGACTGCC[C/T]ACAGTTTATGAATAA | 76577 |
rs46247572 | snp | C/T | 0.32 | 0.24 | utr-variant-3-prime | Faf2 | Mm_Celera | 13:54662388 | TCCCACATGCCAGCG[C/T]GCACTGATAAGTATT | 76577 |
rs46295211 | snp | A/C | 0.32 | 0.24 | intron-variant | Faf2 | Mm_Celera | 13:54649659 | AAACCATGAGAACAG[A/C]TGACTTTCTGTGACT | 76577 |
rs46309552 | snp | C/T | 0.32 | 0.24 | intron-variant | Faf2 | Mm_Celera | 13:54652548 | ACTGATTATAGCTTT[C/T]CTCATTACATGGATT | 76577 |
rs46362857 | snp | G/T | 0.231111 | 0.249285 | utr-variant-3-prime | Faf2 | Mm_Celera | 13:54661905 | GGTGGTGGTAAAGGG[G/T]TCTGAACCAAAGGCT | 76577 |
rs46369133 | snp | A/C | 0.124444 | 0.216185 | synonymous-codon | Faf2 | Mm_Celera | 13:54656396 | GATTCCAGAGTAGAG[A/C]GACGATTCCACTTCT | 76577 |
rs46445798 | snp | A/G | 0.32 | 0.24 | intron-variant | Faf2 | Mm_Celera | 13:54650397 | CATTTAACTTTGTCA[A/G]CAGTCTGAGAGATAA | 76577 |
rs46454016 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Faf2 | Mm_Celera | 13:54623571 | GATTAGCATTAAAGA[A/G]TGAATAAACAGACAG | 76577 |
rs46485412 | snp | A/G | 0.124444 | 0.216185 | synonymous-codon, utr-variant-5-prime | Faf2 | Mm_Celera | 13:54621885 | TCAGGAGCAGACCGA[A/G]AAGCTGCTGCAGTTT | 76577 |
rs46518381 | snp | C/T | | | intron-variant | Faf2 | Mm_Celera | 13:54660656 | CGAGGCCAGCCTGGT[C/T]TACAGAGTGAGTTCC | 76577 |
rs46601885 | snp | C/T | | | intron-variant | Faf2 | Mm_Celera | 13:54657511 | CCTCTGCCTCTGGAG[C/T]TGGGACTAAAGGCAT | 76577 |
rs46613196 | snp | A/G | 0.124444 | 0.216185 | intron-variant, upstream-variant-2KB | Faf2 | Mm_Celera | 13:54644798 | ATTTGACACAGTCTG[A/G]CATGAAGCTGTCTGT | 76577 |
rs46650120 | snp | C/G | 0.32 | 0.24 | utr-variant-3-prime, upstream-variant-2KB | Faf2, LOC105245510 | Mm_Celera | 13:54663216 | TGGGTATGCACCACT[C/G]CATAGGCTTGCCAGT | 76577 |
rs46669374 | snp | A/T | 0.244898 | 0.249948 | intron-variant | Faf2 | Mm_Celera | 13:54645976 | GCCGGCAGATCAGGC[A/T]TAGCATAGAATATGA | 76577 |
rs46671726 | snp | G/T | 0.35503 | 0.226867 | intron-variant | Faf2 | Mm_Celera | 13:54632532 | TCTGATTTAAGAATT[G/T]GGACCTTGTTTTCAA | 76577 |
rs46676409 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Faf2 | Mm_Celera | 13:54650494 | CATACAGTCAGCGTA[A/C]GGTTGTGTTTGAGCA | 76577 |
rs46739937 | snp | C/T | 0.32 | 0.24 | intron-variant | Faf2 | Mm_Celera | 13:54650621 | CTTTTGCTAGGCATT[C/T]GTCTTCTCTATCCAG | 76577 |
rs46747935 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Faf2 | Mm_Celera | 13:54640453 | GGGTGACCTCACTCA[A/G]TTGAGAGATACTGTT | 76577 |
rs46767263 | snp | A/G | | | intron-variant | Faf2 | Mm_Celera | 13:54660678 | TTGGCCTTGAACTCA[A/G]AAAATCCACTTGCCT | 76577 |
rs46776525 | snp | C/T | 0.32 | 0.24 | intron-variant | Faf2 | Mm_Celera | 13:54637914 | AATTCTTAGATTCGC[C/T]GGTTATTGGACCCCT | 76577 |
rs46870213 | snp | C/T | 0.489796 | 0.070696 | intron-variant | Faf2 | Mm_Celera | 13:54656048 | TAACACCATGCCACA[C/T]GTGGTACTCTATGAA | 76577 |
rs46894104 | snp | A/C | 0.32 | 0.24 | intron-variant | Faf2 | Mm_Celera | 13:54649393 | GTAGACTACATTAGC[A/C]ATGCAGGGAATTACA | 76577 |
rs46983889 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Faf2 | Mm_Celera | 13:54640102 | CATGAAGGTTAGGTC[A/T]AGTTACTACCTGCCA | 76577 |
rs47015540 | snp | A/G | 0.32 | 0.24 | intron-variant | Faf2 | Mm_Celera | 13:54652265 | CTGACTTGGGGCTCC[A/G]CAGACTTCTTTCCTG | 76577 |
rs47063704 | snp | A/G | 0.32 | 0.24 | intron-variant | Faf2 | Mm_Celera | 13:54642517 | TTCTAGAGTGGACTA[A/G]TTAACTGCTGCTGTG | 76577 |
rs47146770 | snp | A/T | 0.32 | 0.24 | intron-variant | Faf2 | Mm_Celera | 13:54630634 | ATTTGTGACTAAATA[A/T]TAATGTTTTGGAACT | 76577 |
rs47191394 | snp | G/T | | | intron-variant | Faf2 | Mm_Celera | 13:54633401 | CCTACAAAGTACTTG[G/T]GATTGATTGAAATCC | 76577 |
rs47263243 | snp | A/G | 0.32 | 0.24 | intron-variant, upstream-variant-2KB | Faf2 | Mm_Celera | 13:54644988 | TTGTTATGTGGGAAA[A/G]TCGTTGACCATGAAT | 76577 |
rs47402729 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Faf2 | Mm_Celera | 13:54654199 | TTGTCTTCAGTAGAA[A/G]AGAAAATAGACAGGA | 76577 |
rs47615007 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Faf2 | Mm_Celera | 13:54641362 | ATGCAGTAGTTTCCT[C/T]GTGGGTTTATTTGAG | 76577 |
rs47678386 | snp | A/C | 0.32 | 0.24 | intron-variant | Faf2 | Mm_Celera | 13:54641575 | TTTGTAGCTAGAATA[A/C]CCTCTTTTTAATTTG | 76577 |
rs47978237 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Faf2 | Mm_Celera | 13:54651489 | GTAACATGGCTCTTT[A/G]TAGTGCCTTTTCCTT | 76577 |
rs47979415 | snp | C/T | 0.35503 | 0.226867 | intron-variant | Faf2 | Mm_Celera | 13:54649149 | AGAGCAGCACAGACA[C/T]GTGTTAAAAGGTGGC | 76577 |
rs48034418 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Faf2 | Mm_Celera | 13:54629129 | TTAGTTGTAGGCAAG[A/G]TAATGACTTTGAGGA | 76577 |
rs48063027 | snp | C/T | 0.124444 | 0.216185 | intron-variant, upstream-variant-2KB | Faf2 | Mm_Celera | 13:54644957 | AGTCTAAATATAAGA[C/T]GGAAAGAATGAATAT | 76577 |
rs48079074 | snp | C/T | 0.32 | 0.24 | intron-variant | Faf2 | Mm_Celera | 13:54630998 | AGTCACCTTTAGAGG[C/T]TGGCCAGGGTCACAG | 76577 |
rs48084941 | snp | G/T | 0.32 | 0.24 | intron-variant | Faf2 | Mm_Celera | 13:54631093 | AAGGTGAGCATATTT[G/T]ATTTTTTTTCCTAAA | 76577 |
rs48182788 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Faf2 | Mm_Celera | 13:54646715 | AACTACACAATTTTC[A/G]AAAATCACAGTGAAA | 76577 |
rs48259519 | snp | C/T | | | intron-variant | Faf2 | Mm_Celera | 13:54657213 | GCTGGGAATTGAACT[C/T]AGGACCTCTGGAAAA | 76577 |
rs48268694 | snp | C/T | 0.32 | 0.24 | intron-variant | Faf2 | Mm_Celera | 13:54642441 | GGAGGTGCTTAGAAT[C/T]TGTGGGAGTTCTGAA | 76577 |
rs48270645 | snp | C/G | 0.124444 | 0.216185 | utr-variant-3-prime, upstream-variant-2KB | Faf2, LOC105245510 | Mm_Celera | 13:54663343 | TGAGGCCAGTTCAGT[C/G]TGTGACTCCCAAAGA | 76577 |
rs48320932 | snp | C/T | 0.489796 | 0.070696 | intron-variant | Faf2 | Mm_Celera | 13:54645755 | CTATACCTACTTAGC[C/T]ATAGATTGTTGGCAT | 76577 |
rs48331545 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Faf2 | Mm_Celera | 13:54628598 | TTGTGTGCCGGGGCT[A/G]TAACTGTGGCATTAT | 76577 |
rs48382759 | snp | G/T | 0.48 | 0.0979796 | intron-variant | Faf2 | Mm_Celera | 13:54659567 | ACCATAATTAAATGT[G/T]CATAGTCCTGTCAGT | 76577 |
rs48384257 | snp | C/G | 0.32 | 0.24 | intron-variant | Faf2 | Mm_Celera | 13:54622646 | TGGGAGGATGCCACC[C/G]GGGTGGTGGTAACCA | 76577 |
rs48516820 | snp | C/T | 0.32 | 0.24 | intron-variant | Faf2 | Mm_Celera | 13:54645345 | CTCTGTTTATATGCT[C/T]CTAACAACAAGGTAG | 76577 |
rs48552826 | snp | A/G | 0.32 | 0.24 | intron-variant | Faf2 | Mm_Celera | 13:54660891 | TTCCTGGGGAAGGTT[A/G]GGACATGTGACTTCA | 76577 |
rs48717793 | snp | C/T | 0.408163 | 0.193609 | upstream-variant-2KB | Faf2 | Mm_Celera | 13:54621558 | AATTGCGGGACTCTC[C/T]CGAGCTCCTGGAGGT | 76577 |
rs48755379 | snp | A/G | 0.124444 | 0.216185 | downstream-variant-500B, upstream-variant-2KB | Faf2, LOC105245510 | Mm_Celera | 13:54664348 | AGAGTAAATGAAATC[A/G]TTGACTGTGTATGGA | 76577 |
rs48756165 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Faf2 | Mm_Celera | 13:54624228 | TGGAGTTTAGGGAAG[A/G]GACAACTTGTTGATG | 76577 |
rs48804748 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Faf2 | Mm_Celera | 13:54647385 | GCATGGCATGTTTTA[C/T]TAATTGTAATGCAAT | 76577 |
rs48813295 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Faf2 | Mm_Celera | 13:54645402 | GTAAGCTTGACGCTC[A/T]ATCATTTTTGAGTAG | 76577 |
rs49016104 | snp | C/T | 0.124444 | 0.216185 | upstream-variant-2KB | Faf2 | Mm_Celera | 13:54621331 | AGGTTGGACGAGGTA[C/T]AGAGCTGAGTGTCTG | 76577 |
rs49042660 | snp | A/G | 0.459184 | 0.136902 | intron-variant | Faf2 | Mm_Celera | 13:54638066 | AGCTGTCTCACCAGT[A/G]TTTCCTGCAGCCAGC | 76577 |
rs49112384 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Faf2 | Mm_Celera | 13:54653659 | CCTCCACATGTTGTG[C/T]GGCACGCTTACTCCT | 76577 |
rs49136732 | snp | A/G | 0.459184 | 0.136902 | upstream-variant-2KB | Faf2 | Mm_Celera | 13:54620939 | CGTTTTTATTGGACA[A/G]TATTAGGCTAAGAAG | 76577 |
rs49181433 | snp | A/T | 0.32 | 0.24 | intron-variant | Faf2 | Mm_Celera | 13:54627106 | ATTTGTAGCTAGCTT[A/T]TAAAACTAGTGAGTC | 76577 |
rs49193734 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Faf2 | Mm_Celera | 13:54640941 | TTCCTTCATTTTTGC[A/G]CATGATCTAAGGCTT | 76577 |
rs49201577 | snp | A/G | 0.32 | 0.24 | intron-variant | Faf2 | Mm_Celera | 13:54647537 | AGGGATAGTGTATGG[A/G]CCCATGAGACACTGC | 76577 |
rs49273139 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Faf2 | Mm_Celera | 13:54659616 | TAAACCATTTTAAGG[C/T]GACAGGAGACTGCAT | 76577 |
rs49286390 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Faf2 | Mm_Celera | 13:54645650 | TTCTAACCACCTTAT[C/T]TGTCTCCTGATTTCA | 76577 |
rs49353797 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Faf2 | Mm_Celera | 13:54660038 | TCTCAAAGGGGAAAG[C/T]CCATAATTCCGAGGA | 76577 |
rs49373411 | snp | A/G | 0.244898 | 0.249948 | upstream-variant-2KB | Faf2 | Mm_Celera | 13:54621417 | CCACTGTTTCCCCTA[A/G]TAAGGCAGACCAACT | 76577 |
rs49402681 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Faf2 | Mm_Celera | 13:54628578 | TATGTGGGTCCAGTC[A/T]TCATTTGTGTGCCGG | 76577 |
rs49421224 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Faf2 | Mm_Celera | 13:54633749 | TTTCTACAGTGTTGT[C/T]TCAGTCACTCAGGTA | 76577 |
rs49485215 | snp | C/T | 0.32 | 0.24 | intron-variant | Faf2 | Mm_Celera | 13:54660281 | ATGGTACTTCAAGTT[C/T]CCCACTGTGGGATTT | 76577 |
rs49490859 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Faf2 | Mm_Celera | 13:54650696 | GAGCGCAGACAGCCA[A/G]TGCAGGGAGTTCAGT | 76577 |
rs49572732 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Faf2 | Mm_Celera | 13:54637927 | GCTGGTTATTGGACC[C/T]CTGAAGGGAAATAGT | 76577 |
rs49735219 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Faf2 | Mm_Celera | 13:54641363 | TGCAGTAGTTTCCTC[A/G]TGGGTTTATTTGAGC | 76577 |
rs49742949 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Faf2 | Mm_Celera | 13:54642209 | ATATGTTCTTTGTGA[C/T]CCAAGTTCCCTTGAC | 76577 |
rs49797130 | snp | C/T | 0.231111 | 0.249285 | synonymous-codon | Faf2 | Mm_Celera | 13:54661115 | AGAAGTTCTCTTTGT[C/T]CAGGACCTGACAGAC | 76577 |
rs49859177 | snp | A/G | 0.32 | 0.24 | intron-variant | Faf2 | Mm_Celera | 13:54624708 | GGAGAGGTTTAACAC[A/G]GGAGTAACAACACCA | 76577 |
rs49885171 | snp | C/T | 0.32 | 0.24 | intron-variant | Faf2 | Mm_Celera | 13:54645731 | CCCAGTAGATTTTCT[C/T]GCTCAAGACTATACC | 76577 |
rs49912271 | snp | A/G | 0.32 | 0.24 | intron-variant, upstream-variant-2KB | Faf2 | Mm_Celera | 13:54645089 | AAATGATAGATACCA[A/G]AGCAGTAGCATTTAA | 76577 |
rs49977027 | snp | A/G | 0.32 | 0.24 | intron-variant | Faf2 | Mm_Celera | 13:54633077 | ATAAGAACTTGAGAT[A/G]TGGGAAGAGAGACAC | 76577 |
rs49994274 | snp | C/T | 0.32 | 0.24 | intron-variant | Faf2 | Mm_Celera | 13:54630986 | TCTGAGCAGAGGAGT[C/T]ACCTTTAGAGGCTGG | 76577 |
rs50016848 | snp | A/G | 0.32 | 0.24 | utr-variant-3-prime | Faf2 | Mm_Celera | 13:54662656 | CCCATGACTATCCCC[A/G]AGGCCCTAGCGCAGG | 76577 |
rs50072354 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Faf2 | Mm_Celera | 13:54645671 | CCTGATTTCATACTC[C/T]AGGAACTTTTGTCCC | 76577 |
rs50106827 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Faf2 | Mm_Celera | 13:54623591 | TAAACAGACAGCTTT[C/T]ACTGCTTTGTAGAGC | 76577 |