SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs6278472 | snp | C/T | 0.5 | 0 | intron-variant | Apaf1 | Mm_Celera | 10:91055810 | CAAAATCAAAGGGCA[C/T]AGCAAGAAGATGATC | 11783 |
rs6278571 | snp | C/T | 0.5 | 0 | intron-variant | Apaf1 | Mm_Celera | 10:91055882 | TCAAAATGAGACATG[C/T]NTTAGCTACTAAACT | 11783 |
rs6278572 | snp | C/T | 0.5 | 0 | intron-variant | Apaf1 | Mm_Celera | 10:91055883 | CAAAATGAGACATGN[C/T]TTAGCTACTAAACTT | 11783 |
rs6304319 | snp | A/T | 0.5 | 0 | intron-variant | Apaf1 | Mm_Celera | 10:91051568 | TCCTGAGGGAGAAAG[A/T]ACTGAATCTGTCCAT | 11783 |
rs13472986 | snp | A/G | 0.197531 | 0.244432 | utr-variant-3-prime | Apaf1 | GRCm38.p3 | 10:90989445 | TATGAAGGTGGTTTT[A/G]TATCATGTTTTATGT | 11783 |
rs13480702 | snp | C/T | 0.492188 | 0.0620098 | synonymous-codon | Apaf1 | Mm_Celera | 10:91060255 | AAAATCACGTAAAAG[C/T]GCACCAATTAAAGAC | 11783 |
rs29313112 | snp | C/T | 0.5 | 0 | intron-variant | Apaf1 | Mm_Celera | 10:91078342 | AAGGTGGCTCACAAC[C/T]ATCTGTAATGAAATC | 11783 |
rs29313450 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Apaf1 | Mm_Celera | 10:91056964 | ACGTGCCTTTAATCC[C/T]GGCACTCTAGAGATG | 11783 |
rs29313952 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Apaf1 | Mm_Celera | 10:91051800 | CACTACTGACCAGCT[C/T]GAACTTTAACTAAGA | 11783 |
rs29315101 | snp | G/T | 0.48 | 0.0979796 | intron-variant | Apaf1 | Mm_Celera | 10:91020553 | GGATAGATATGTACC[G/T]AGGAGCTTTGTTTCT | 11783 |
rs29316289 | snp | C/G | 0.5 | 0 | downstream-variant-500B | Apaf1 | Mm_Celera | 10:90988835 | GAGGAGGCCTGAGAA[C/G]AGAATCAGGTGTCGT | 11783 |
rs29320883 | snp | A/G | 0.5 | 0 | upstream-variant-2KB, intron-variant | Apaf1, Ikbip | Mm_Celera | 10:91083719 | TATTCTTGTTTATGT[A/G]TATGAGTGTCAGTGT | 11783 |
rs29321383 | snp | A/G | 0.497041 | 0.0383476 | intron-variant | Apaf1 | Mm_Celera | 10:91033958 | CATCAGCTGAAGACC[A/G]GTAATAAAGTATACA | 11783 |
rs29321530 | snp | A/G | 0.5 | 0 | intron-variant | Apaf1 | Mm_Celera | 10:91051827 | AAGAGTAATGGGTAC[A/G]GTGGAGAGATAAAGG | 11783 |
rs29322687 | snp | C/T | 0.5 | 0 | intron-variant | Apaf1 | Mm_Celera | 10:90998380 | GCTCGCTCGTCCACA[C/T]AGCATCACCGGCTGG | 11783 |
rs29322947 | snp | C/T | 0.5 | 0 | intron-variant | Apaf1 | Mm_Celera | 10:91020130 | GGAGGAGCGGGACAG[C/T]AGACTTAGAAGGGTC | 11783 |
rs29323060 | snp | C/T | 0.5 | 0 | intron-variant | Apaf1 | GRCm38.p3 | 10:91071051 | GGAGGCAGAGGCAGG[C/T]GGATTTCTAAGTTCG | 11783 |
rs29323256 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Apaf1 | Mm_Celera | 10:91044638 | CAAACTTATTCACAA[A/G]ATAGAAACAGAGGGA | 11783 |
rs29323351 | snp | C/T | 0.5 | 0 | intron-variant | Apaf1 | Mm_Celera | 10:91044923 | AAACTGAAAGAACAA[C/T]AAAACCCACATGATC | 11783 |
rs29325192 | snp | A/G | 0.48 | 0.0979796 | upstream-variant-2KB | Apaf1, Ikbip | Mm_Celera | 10:91082756 | CACAGCGCGCGCCCG[A/G]GCACGCAAATTCACT | 11783 |
rs29325959 | snp | C/T | 0.5 | 0 | intron-variant | Apaf1 | Mm_Celera | 10:91073010 | AAGTTCATCACAAAA[C/T]TGAAATGAAAACATA | 11783 |
rs29326253 | snp | A/G | 0.375 | 0.216506 | intron-variant | Apaf1 | Mm_Celera | 10:91051261 | CAAAGCTCAGACAGC[A/G]ACCTTCACAGAGACG | 11783 |
rs29326494 | snp | A/G | 0.375 | 0.216506 | intron-variant | Apaf1 | Mm_Celera | 10:91057263 | GTTGAGGGTAGCCAC[A/G]ACACGAGGAAATGTA | 11783 |
rs29326558 | snp | A/G | 0.492188 | 0.0620098 | intron-variant | Apaf1 | Mm_Celera | 10:91051068 | TAGCAAAGTTAAGGC[A/G]ACTTCATTAAGACTA | 11783 |
rs29328529 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Apaf1 | Mm_Celera | 10:91008544 | AAGCTCAGAGCCTCG[A/G]TATATATAATTATGG | 11783 |
rs29329495 | snp | A/G | 0.5 | 0 | intron-variant, upstream-variant-2KB | Apaf1, Ikbip | Mm_Celera | 10:91082135 | CAGAACTTGCAAAGA[A/G]CCTGCCCAGAGGAGC | 11783 |
rs29330018 | snp | C/T | 0.5 | 0 | upstream-variant-2KB, intron-variant | Apaf1, Ikbip | Mm_Celera | 10:91083897 | TTGAACTGTATGTAA[C/T]ATTGTAAAGAATATG | 11783 |
rs29330346 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Apaf1 | Mm_Celera | 10:91049860 | AAAGGTCAGAAAACG[C/G]CACGATATCCCCTGG | 11783 |
rs29330444 | snp | C/T | 0.5 | 0 | intron-variant | Apaf1 | Mm_Celera | 10:91060323 | GTGATTACATTAATA[C/T]CATCTTAGTTAAAAA | 11783 |
rs29331262 | snp | A/C | 0.5 | 0 | intron-variant | Apaf1 | Mm_Celera | 10:91050309 | TACATATGACACTGC[A/C]CCTACCACTATATGA | 11783 |
rs29331263 | snp | A/G | 0.5 | 0 | intron-variant | Apaf1 | Mm_Celera | 10:91020119 | GATCATACGGTGGAG[A/G]AGCGGGACAGCAGAC | 11783 |
rs29331898 | snp | A/C | 0.5 | 0 | intron-variant | Apaf1 | Mm_Celera | 10:91006245 | AAAATATTTCTAAAA[A/C]TTATTTCTCCCTCTG | 11783 |
rs29331925 | snp | C/T | 0.5 | 0 | intron-variant | Apaf1 | Mm_Celera | 10:91056318 | ATGACACAAAACAAG[C/T]ATATGTGCTTGTGCC | 11783 |
rs29332030 | snp | A/G | 0.5 | 0 | upstream-variant-2KB, intron-variant | Apaf1, Ikbip | Mm_Celera | 10:91083784 | CGCAAGAGAGTGTCA[A/G]ATCCAAGAAGCTGGA | 11783 |
rs29332408 | snp | C/G | 0.375 | 0.216506 | intron-variant | Apaf1 | Mm_Celera | 10:91079791 | TCTGGTGTGGTTGAA[C/G]ACAGCTACAGTGTGC | 11783 |
rs29333999 | snp | C/T | 0.5 | 0 | intron-variant | Apaf1 | Mm_Celera | 10:91033644 | TTTTACAGCTCCTAT[C/T]CTCTCAGACAGTAAA | 11783 |
rs29334405 | snp | A/G | 0.5 | 0 | upstream-variant-2KB, intron-variant | Apaf1, Ikbip | Mm_Celera | 10:91084549 | ACTGGGTAATGCTTG[A/G]GTACTGGGTTTTGTT | 11783 |
rs29336226 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Apaf1 | Mm_Celera | 10:90997538 | TTACTCAAGTAAAAA[A/T]TAGCTCAAGGACCAG | 11783 |
rs29337062 | snp | A/C | 0.492188 | 0.0620098 | intron-variant | Apaf1 | Mm_Celera | 10:91033844 | ACTCACACACGAATA[A/C]AGAAATCAAACACCT | 11783 |
rs29337118 | snp | C/T | 0.5 | 0 | intron-variant | Apaf1 | Mm_Celera | 10:91004597 | TTCTAGTCTTAACAG[C/T]CTGGGCTGTGCCTAA | 11783 |
rs29337570 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Apaf1 | Mm_Celera | 10:91050063 | GAGAGATGGCTCAGC[A/G]GTTAAGAGCCCTGAT | 11783 |
rs29337573 | snp | C/T | 0.5 | 0 | intron-variant | Apaf1 | Mm_Celera | 10:90998388 | GTCCACATAGCATCA[C/T]CGGCTGGGTGTTTCA | 11783 |
rs29338686 | snp | A/C | 0.345679 | 0.230967 | intron-variant | Apaf1 | Mm_Celera | 10:91001772 | CAGAAATTTCTATGT[A/C]GTGTCAATATGCGGA | 11783 |
rs29339127 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Apaf1 | Mm_Celera | 10:91066057 | CCCCACAGGCTCATG[A/G]ATTTGAATATTTAGC | 11783 |
rs29339618 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Apaf1 | Mm_Celera | 10:91002844 | GCACTAAAGCATCCA[C/T]ACTTTGGTCTTCCTT | 11783 |
rs29340023 | snp | C/T | 0.5 | 0 | upstream-variant-2KB, intron-variant | Apaf1, Ikbip | Mm_Celera | 10:91084687 | TAAATGTGTTGGATT[C/T]GCTGTTTTAAATAAA | 11783 |
rs29340119 | snp | C/G | 0.5 | 0 | intron-variant | Apaf1 | Mm_Celera | 10:90998389 | TCCACATAGCATCAC[C/G]GGCTGGGTGTTTCAA | 11783 |
rs29340147 | snp | A/G | 0.5 | 0 | utr-variant-5-prime, upstream-variant-2KB | Apaf1, Ikbip | Mm_Celera | 10:91082699 | CTGGTCTCTGCCTCA[A/G]GACCGCGGAGCACTC | 11783 |
rs29340347 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Apaf1 | Mm_Celera | 10:91044524 | CTAGTTAAATAGAAG[C/T]AGTCATTAAAGTCTG | 11783 |
rs29341424 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Apaf1 | Mm_Celera | 10:91001566 | GACAATGGATCACGG[A/G]GCTTCTGAGCTGCCC | 11783 |
rs29341648 | snp | A/T | 0.48 | 0.0979796 | intron-variant | Apaf1 | Mm_Celera | 10:91062587 | GTATGGTTCCCTGCC[A/T]GCTGCCTGTGGGTCA | 11783 |
rs29341977 | snp | A/C | 0.5 | 0 | intron-variant | Apaf1 | Mm_Celera | 10:91005696 | CTTAGAAAAAAAAAA[A/C]AAAAACAGTGTTTCT | 11783 |
rs29342263 | snp | A/G | 0.5 | 0 | intron-variant | Apaf1 | Mm_Celera | 10:91076017 | AATTTTTTAAAAAAT[A/G]AAGTGGAATTGTTTA | 11783 |
rs29342805 | snp | A/C | 0.260355 | 0.249785 | intron-variant | Apaf1 | Mm_Celera | 10:91021405 | CTGAGTCATCCTTGG[A/C]TACAGAGTGAATGTG | 11783 |
rs29342812 | snp | C/T | 0.5 | 0 | intron-variant | Apaf1 | Mm_Celera | 10:91065022 | TCTCACTCTATGGTC[C/T]AGGCTATCCTCAAAC | 11783 |
rs29343075 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Apaf1 | Mm_Celera | 10:91007687 | TGAGTTCAAGGCTAG[C/T]CTGGTCTACAGAGTG | 11783 |
rs29343190 | snp | A/G | 0.5 | 0 | synonymous-codon | Apaf1 | Mm_Celera | 10:91059621 | ATCTACTTGAAGATC[A/G]TGTAAATAATAACAA | 11783 |
rs29343884 | snp | C/T | 0.5 | 0 | intron-variant | Apaf1 | Mm_Celera | 10:91002337 | TATTCCATCCCTCCT[C/T]CCCCTGCCTCTCTGA | 11783 |
rs29344494 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Apaf1 | Mm_Celera | 10:91005470 | ACTAAAATTAAGCCA[A/G]GTATGACAGCACACA | 11783 |
rs29344764 | snp | A/G | 0.5 | 0 | intron-variant | Apaf1 | Mm_Celera | 10:91012067 | TCCACCTATAGGGTT[A/G]CAGTTCCCTTTAGCT | 11783 |
rs29345005 | snp | A/C | 0.5 | 0 | intron-variant | Apaf1 | Mm_Celera | 10:91002304 | CTGCTTCCCAGGTCT[A/C]TACTTCACCAAACCT | 11783 |
rs29345740 | snp | C/T | 0.5 | 0 | intron-variant | Apaf1 | Mm_Celera | 10:91036804 | GTTGTTTATCTCAGG[C/T]TTGTGTCCCAGCTTT | 11783 |
rs29347579 | snp | C/G | 0.48 | 0.0979796 | intron-variant | Apaf1 | Mm_Celera | 10:91062638 | TTCTCTCAGTGCCAC[C/G]CCTGCTTGCTTTCTG | 11783 |
rs29347856 | snp | A/G | 0.375 | 0.216506 | intron-variant | Apaf1 | Mm_Celera | 10:91006478 | GCCAAACTTCATCCC[A/G]ACCCTGCACCTTCTC | 11783 |
rs29349443 | snp | C/G | 0.5 | 0 | intron-variant | Apaf1 | Mm_Celera | 10:91078162 | CTGTAAGTGTGAGGA[C/G]CCAAGTTCTAATCCA | 11783 |
rs29349599 | snp | A/T | 0.5 | 0 | intron-variant | Apaf1 | Mm_Celera | 10:91002375 | CCCCCACCCACCCAC[A/T]CACCCACCCACTCCC | 11783 |
rs29349679 | snp | C/T | 0.5 | 0 | intron-variant | Apaf1 | GRCm38.p3 | 10:91058167 | CAGCATACAAATACA[C/T]GCAGCCACAACATTC | 11783 |
rs29351942 | snp | C/T | 0.375 | 0.216506 | intron-variant | Apaf1 | Mm_Celera | 10:91044657 | GAAACAGAGGGACAC[C/T]GCCCAATTCATGTCA | 11783 |
rs29352565 | snp | C/T | 0.48 | 0.0979796 | upstream-variant-2KB | Apaf1, Ikbip | Mm_Celera | 10:91082912 | CGTGGCACTCTCGGC[C/T]CCGCCCCCTCTACGC | 11783 |
rs29352917 | snp | G/T | 0.48 | 0.0979796 | intron-variant | Apaf1 | Mm_Celera | 10:91073819 | TTAAATAAGACTCAC[G/T]AAAAAATGAAGGAGC | 11783 |
rs29354788 | snp | C/T | 0.5 | 0 | intron-variant | Apaf1 | Mm_Celera | 10:91002305 | TGCTTCCCAGGTCTA[C/T]ACTTCACCAAACCTC | 11783 |
rs29356278 | snp | A/T | 0.484429 | 0.0868505 | intron-variant | Apaf1 | Mm_Celera | 10:91049529 | TCAATGATTGAGGAT[A/T]GAAGCAACATTTTTC | 11783 |
rs29356285 | snp | G/T | 0.5 | 0 | intron-variant | Apaf1 | Mm_Celera | 10:91061293 | AAGGCTGAGATTGTG[G/T]TTTCTTGTTTCCCTC | 11783 |
rs29356422 | snp | G/T | 0.5 | 0 | intron-variant | Apaf1 | Mm_Celera | 10:91036600 | GTTAGGCCCTTAACA[G/T]GTACCCTTGAAGGGA | 11783 |
rs29357378 | snp | C/T | 0.5 | 0 | intron-variant | Apaf1 | Mm_Celera | 10:91067296 | AAAGAAATGTAAGGC[C/T]TCCGAACAAGAGCCC | 11783 |
rs29358119 | snp | C/T | 0.444444 | 0.157135 | downstream-variant-500B | Apaf1 | Mm_Celera | 10:90988945 | GTCAGCAAATCCTAG[C/T]GATCCCCCTGTCTCT | 11783 |
rs29358361 | snp | C/T | 0.5 | 0 | intron-variant | Apaf1 | Mm_Celera | 10:91036220 | TCAAAAATAACAGTA[C/T]GACAAAGGTTCTTAG | 11783 |
rs29359097 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Apaf1 | Mm_Celera | 10:91016735 | TTTGTCAGTGAAACT[C/G]TCCTCTAAACTCTTG | 11783 |
rs29360791 | snp | C/T | 0.487535 | 0.077957 | intron-variant | Apaf1 | Mm_Celera | 10:90998277 | AGGTCTAAAATGATG[C/T]GCTGCACCTTGCACA | 11783 |
rs29360810 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Apaf1 | Mm_Celera | 10:91061258 | GCGATCTGTGCTGTC[A/G]AAGTCTAGTAAGAGA | 11783 |
rs29361813 | snp | A/T | 0.5 | 0 | intron-variant | Apaf1 | Mm_Celera | 10:91050400 | GGACAGATAAAGCAA[A/T]GTCATTTTCTTCCTA | 11783 |
rs29362053 | snp | C/T | 0.5 | 0 | intron-variant | Apaf1 | Mm_Celera | 10:91036455 | TTCATTACCACTTCA[C/T]AACTAATTGTGCCAC | 11783 |
rs29362094 | snp | A/G | 0.5 | 0 | synonymous-codon | Apaf1 | Mm_Celera | 10:91049397 | AGAAGCTATTCTCTG[A/G]CCATCCTGAGAAAAA | 11783 |
rs29362705 | snp | A/T | 0.5 | 0 | intron-variant | Apaf1 | Mm_Celera | 10:91053693 | CACAAAAGTAGTATT[A/T]AAAAAATTATTATTT | 11783 |
rs29362956 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Apaf1 | Mm_Celera | 10:91057586 | GTGGCACACACCTTC[A/G]ATCCCAACACTTGGG | 11783 |
rs29363102 | snp | A/G | 0.475309 | 0.108333 | utr-variant-3-prime | Apaf1 | Mm_Celera | 10:90990642 | AGAGAGAGAGGTGCT[A/G]TTGGCACACGCCTTC | 11783 |
rs29363925 | snp | C/T | 0.5 | 0 | intron-variant | Apaf1 | Mm_Celera | 10:91020513 | CAGGGGAAGGACACA[C/T]AGCTCACAGAATAGC | 11783 |
rs29364639 | snp | A/G | 0.207612 | 0.24638 | intron-variant | Apaf1 | Mm_Celera | 10:90991642 | ACTGGTAATCCCACC[A/G]CATGGTAATTTGTAA | 11783 |
rs29365842 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Apaf1 | Mm_Celera | 10:91062623 | TAAAGCTCTCAGCTA[C/T]TCTCTCAGTGCCACG | 11783 |
rs29366121 | snp | C/T | 0.46875 | 0.121031 | intron-variant | Apaf1 | Mm_Celera | 10:91033580 | TGGTTATCTACATGA[C/T]ACCCTACAACAAGCT | 11783 |
rs29366566 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Apaf1 | Mm_Celera | 10:91049891 | AACTGGGGCTACAGA[C/T]GGTTGTGAGTCACCG | 11783 |
rs29366756 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Apaf1 | GRCm38.p3 | 10:91049998 | TTCTTTATACACATT[A/T]ATATAATATATGTAA | 11783 |
rs29367062 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Apaf1 | Mm_Celera | 10:91056794 | CCACAAACTCAAAGC[A/G]AGAAAAGAATAGGAG | 11783 |
rs29368033 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Apaf1 | Mm_Celera | 10:91017608 | GAAATGCGGTGCTGG[C/T]CTCTGTGGATACTGC | 11783 |
rs29368779 | snp | G/T | 0.375 | 0.216506 | intron-variant | Apaf1 | Mm_Celera | 10:91033789 | CAACACAGGCAGGTC[G/T]CCCTGAGTGGAGTGA | 11783 |
rs29368828 | snp | A/C | 0.48 | 0.0979796 | intron-variant | Apaf1 | Mm_Celera | 10:91057691 | CACAGAGAAACCCTG[A/C]CTCAAAAAACTAAAC | 11783 |
rs29368992 | snp | C/T | 0.5 | 0 | intron-variant | Apaf1 | Mm_Celera | 10:91077990 | GGCCCTCTGGCCTCT[C/T]TTGTCTTTGTTGAAT | 11783 |
rs29369407 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Apaf1 | Mm_Celera | 10:91066914 | ATTCTCAAAACCGTA[C/T]AATGACACATAAGAA | 11783 |
rs29369944 | snp | A/G | 0.5 | 0 | intron-variant | Apaf1 | Mm_Celera | 10:91008854 | AAAATAAATTACATA[A/G]AAATGGCAAAAATAT | 11783 |
rs29370028 | snp | A/G | 0.375 | 0.216506 | intron-variant | Apaf1 | Mm_Celera | 10:90994728 | TTTCAGTAAACATCA[A/G]CCAACTCACAGAATC | 11783 |