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 |
rs29370131 | snp | G/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | Apaf1, Ikbip | Mm_Celera | 10:91082068 | ACAAGAGCAGGAGGA[G/T]GATTACCAAACATCC | 11783 |
rs29371106 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Apaf1 | Mm_Celera | 10:91049768 | GTCACTTTCTATTTT[C/T]TCCTTTTAAAAAAAC | 11783 |
rs29372674 | snp | A/G | 0.5 | 0 | intron-variant | Apaf1 | Mm_Celera | 10:91037451 | TCCAGAGAACTCAAT[A/G]CCTTCTGCTGTGGCT | 11783 |
rs29373009 | snp | A/G | 0.5 | 0 | intron-variant | Apaf1 | Mm_Celera | 10:91036538 | ATGACCCACAAGTTG[A/G]GAACCACTGTTTTAG | 11783 |
rs29373819 | snp | A/G | 0.5 | 0 | intron-variant, upstream-variant-2KB | Apaf1, Ikbip | Mm_Celera | 10:91082148 | GAGCCTGCCCAGAGG[A/G]GCTTGGGGAGGTGAG | 11783 |
rs29373844 | snp | A/T | 0.5 | 0 | intron-variant | Apaf1 | Mm_Celera | 10:91056258 | AATATGAAACAGAAA[A/T]TTTTTTAGAAATATA | 11783 |
rs29374256 | snp | C/T | 0.5 | 0 | intron-variant | Apaf1 | Mm_Celera | 10:91004445 | ATTAACTCAAACAAA[C/T]CAGTAGCCTTCCTAC | 11783 |
rs29374299 | snp | A/G | 0.5 | 0 | intron-variant | Apaf1 | Mm_Celera | 10:91050743 | CAGGAGAAACAGCAA[A/G]TAACAAGAGACCTTA | 11783 |
rs29374404 | snp | C/G | 0.48 | 0.0979796 | intron-variant | Apaf1 | Mm_Celera | 10:91044858 | ATCATCCCAGAGATG[C/G]AGGGATGATTCAATA | 11783 |
rs29375311 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Apaf1 | GRCm38.p3 | 10:91066291 | GACCAGGGGGGTTGT[A/G]GGATTGTTCCAGCAG | 11783 |
rs29375856 | snp | C/T | 0.5 | 0 | intron-variant | Apaf1 | Mm_Celera | 10:91056703 | CATCAAGGAAAAAGA[C/T]AAGCTAAGAGCCGAG | 11783 |
rs29376032 | snp | C/T | 0.5 | 0 | intron-variant | Apaf1 | Mm_Celera | 10:91052059 | AGAAGTTCGGTAAAT[C/T]CCCCCTAGTGATACA | 11783 |
rs29377944 | snp | A/G | 0.5 | 0 | intron-variant | Apaf1 | Mm_Celera | 10:91020514 | AGGGGAAGGACACAC[A/G]GCTCACAGAATAGCA | 11783 |
rs29378096 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Apaf1 | Mm_Celera | 10:90998463 | CCACCAGTCAGTGGG[C/T]GTGGCCTTTGGGAAC | 11783 |
rs29378886 | snp | C/T | 0.48 | 0.0979796 | upstream-variant-2KB | Apaf1, Ikbip | Mm_Celera | 10:91082807 | GGCCGCGCGCGCGCG[C/T]CCCGCCCGGCGCGTG | 11783 |
rs29379167 | snp | A/G | 0.5 | 0 | intron-variant | Apaf1 | Mm_Celera | 10:91036809 | TTATCTCAGGTTTGT[A/G]TCCCAGCTTTGGAAC | 11783 |
rs29379984 | snp | A/G | 0.375 | 0.216506 | intron-variant | Apaf1 | Mm_Celera | 10:91034096 | AGGCCCAGGCAACAC[A/G]GCAGCTGAAGGTGTG | 11783 |
rs29380488 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Apaf1 | Mm_Celera | 10:91059503 | ACCACGCCCAGCCGG[A/T]ATGTCTTTATATAGC | 11783 |
rs29381984 | snp | G/T | 0.5 | 0 | upstream-variant-2KB, intron-variant | Apaf1, Ikbip | Mm_Celera | 10:91083747 | TGTATTTGTGCACGT[G/T]TGTGCAGGTGCGCGA | 11783 |
rs29382475 | snp | G/T | 0.444444 | 0.157135 | utr-variant-5-prime, upstream-variant-2KB | Apaf1, Ikbip | Mm_Celera | 10:91082226 | GAAGAGCAGCCGGGG[G/T]AGGGTCACTGATGAT | 11783 |
rs29382528 | snp | C/T | 0.444444 | 0.157135 | downstream-variant-500B | Apaf1 | Mm_Celera | 10:90989088 | GGTTTCTCCATGTAG[C/T]CCTGGCTGTCCTGAA | 11783 |
rs29383445 | snp | A/G | 0.5 | 0 | intron-variant | Apaf1 | Mm_Celera | 10:91060574 | CAGGCTGTCAGGCTT[A/G]GCAGCAAGCATCTTT | 11783 |
rs30869795 | snp | C/T | 0.5 | 0 | intron-variant | Apaf1 | Mm_Celera | 10:91030350 | CAGTCCCTCAATGAG[C/T]TTATATATAAATATA | 11783 |
rs33849442 | snp | G/T | 0.484429 | 0.0868505 | utr-variant-3-prime | Apaf1 | Mm_Celera | 10:90989580 | CTCCAGAGCTGCTGC[G/T]TGTGAGCCACAGCCA | 11783 |
rs33850396 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Apaf1 | Mm_Celera | 10:91036243 | GTTCTTAGCAGCTGA[A/C]AGGAAAGCCTTCCTT | 11783 |
rs33857601 | snp | C/T | 0.444444 | 0.157135 | upstream-variant-2KB, intron-variant | Apaf1, Ikbip | Mm_Celera | 10:91084169 | CAGTAGTGGGGGCAC[C/T]GCCATCCCGCTCAAC | 11783 |
rs33857780 | snp | A/G | 0.5 | 0 | intron-variant | Apaf1 | Mm_Celera | 10:91057895 | GCACACGTCATACAT[A/G]AAAATCTTCAGATTC | 11783 |
rs36242923 | snp | A/G | 0.165289 | 0.235211 | intron-variant | Apaf1 | Mm_Celera | 10:91011066 | TTGTGTATCACCTTG[A/G]TTGGCACTATGTCTG | 11783 |
rs36259623 | snp | A/G | 0.197531 | 0.244432 | intron-variant | Apaf1 | Mm_Celera | 10:91018940 | GTTCCACCAAACGAC[A/G]TTTCCGGTATTTTTA | 11783 |
rs36260951 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Apaf1 | Mm_Celera | 10:90994296 | ATAGAGCCCAGAGAA[C/T]ATAGAAGCTCGGTGT | 11783 |
rs36261095 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Apaf1 | Mm_Celera | 10:91004706 | AAAGGTGATGACAAC[A/G]GTGCTTTTAGCTGGA | 11783 |
rs36263093 | snp | C/T | 0.46875 | 0.121031 | intron-variant | Apaf1 | Mm_Celera | 10:91001207 | TGTAGTCTTAATTCT[C/T]GTCACAGTGTTTCAA | 11783 |
rs36265341 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Apaf1 | Mm_Celera | 10:90994274 | AGAGAGTTATGTGGG[A/G]CATTCTATAGAGCCC | 11783 |
rs36268103 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Apaf1 | Mm_Celera | 10:90994650 | CTCATAACCAAAGAC[A/G]CCACTCAAACACAGC | 11783 |
rs36271305 | snp | A/C | 0.277778 | 0.248452 | intron-variant | Apaf1 | Mm_Celera | 10:90999258 | CCAGCCAGACAACTC[A/C]CAGCCTGTAAAAGGT | 11783 |
rs36273992 | snp | A/T | 0.493827 | 0.0552116 | intron-variant | Apaf1 | Mm_Celera | 10:91000381 | GGTGACCACACTGAA[A/T]AGAAAACAGGCACAA | 11783 |
rs36283436 | snp | C/T | 0.375 | 0.216506 | intron-variant | Apaf1 | Mm_Celera | 10:91030398 | TCTAATACCTCTGTG[C/T]CATGCTTTTTAAAAT | 11783 |
rs36304993 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Apaf1 | Mm_Celera | 10:91038672 | TAAAATGTTTCACAT[A/G]CACCTCCTAAAAATC | 11783 |
rs36324571 | snp | C/T | 0.21875 | 0.248039 | intron-variant | Apaf1 | Mm_Celera | 10:91064967 | ACCCACTGGGCCAAC[C/T]GCCATGACTGTCTTA | 11783 |
rs36335772 | snp | A/C | 0.165289 | 0.235211 | intron-variant | Apaf1 | Mm_Celera | 10:90999539 | TCTTAAAAACACACG[A/C]TACAGACATGTAAAC | 11783 |
rs36336057 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Apaf1 | Mm_Celera | 10:91027583 | GAAAGCTCTCTTCTG[C/T]GGAGGGAAACTCATC | 11783 |
rs36340182 | snp | G/T | 0.21875 | 0.248039 | intron-variant | Apaf1 | Mm_Celera | 10:91042952 | TCATAGGAAACTTTT[G/T]ACAACTTAGCAATAA | 11783 |
rs36354513 | snp | A/C | 0.493827 | 0.0552116 | upstream-variant-2KB, intron-variant | Apaf1, Ikbip | Mm_Celera | 10:91083481 | TATTAAGCATCTACT[A/C]CTGCACGTCACAAGT | 11783 |
rs36354655 | snp | C/T | 0.32 | 0.24 | intron-variant | Apaf1 | Mm_Celera | 10:90996109 | CACTGAAATTCTATG[C/T]AATATGTGAATAAGA | 11783 |
rs36361273 | snp | A/C | 0.32 | 0.24 | intron-variant | Apaf1 | Mm_Celera | 10:90995640 | TCACACCCTCGAGTA[A/C]CGCTTACCTTGAGAT | 11783 |
rs36368318 | snp | C/G | 0.391111 | 0.206368 | intron-variant | Apaf1 | Mm_Celera | 10:90991614 | GTTGAGAGAAAAAGA[C/G]AACTTTTGTTAGACT | 11783 |
rs36375009 | snp | G/T | 0.165289 | 0.235211 | intron-variant | Apaf1 | Mm_Celera | 10:91049082 | GATGGAGTCTGCATG[G/T]CTGTTCATTACTGCC | 11783 |
rs36375777 | snp | A/G | 0.375 | 0.216506 | intron-variant | Apaf1 | Mm_Celera | 10:90993789 | TGCCTTCAGGTGTAT[A/G]AGTTATTATAATCTT | 11783 |
rs36376457 | snp | G/T | 0.408163 | 0.193609 | intron-variant | Apaf1 | Mm_Celera | 10:91032968 | GACAACTGTGTCTAC[G/T]CTGTGTAAAATAAAA | 11783 |
rs36378500 | snp | C/G | 0.142012 | 0.225474 | intron-variant | Apaf1 | Mm_Celera | 10:90992939 | GTGCCCTTTGCAGTA[C/G]AACCGGATAAGACAC | 11783 |
rs36387375 | snp | A/G | 0.426035 | 0.177515 | intron-variant | Apaf1 | Mm_Celera | 10:90995925 | AGAAGAGTGTGCTGG[A/G]TCAGAATGTTATCAG | 11783 |
rs36405976 | snp | G/T | 0.48 | 0.0979796 | intron-variant | Apaf1 | Mm_Celera | 10:91047171 | ATGATAAATGACATG[G/T]GCAAAGCTGCCAGGC | 11783 |
rs36409431 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Apaf1 | Mm_Celera | 10:90997457 | ACGTTTGGTGGTGTA[A/G]GCTTTCACAAGATGC | 11783 |
rs36414172 | snp | A/T | 0.375 | 0.216506 | intron-variant | Apaf1 | Mm_Celera | 10:91041515 | GTCTATCTATTGATG[A/T]CAGGCCAATTCACTA | 11783 |
rs36415121 | snp | C/T | 0.277778 | 0.248452 | upstream-variant-2KB, intron-variant | Apaf1, Ikbip | Mm_Celera | 10:91084551 | TGGGTAATGCTTGAG[C/T]ACTGGGTTTTGTTAT | 11783 |
rs36419962 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Apaf1 | Mm_Celera | 10:91019273 | AACGGTTGCTATTAC[A/G]TGAGTTGTGGGCTCT | 11783 |
rs36437265 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Apaf1 | Mm_Celera | 10:90994132 | GACTACACATACAGT[C/T]TATAGCTTCTTCCAG | 11783 |
rs36443044 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Apaf1 | Mm_Celera | 10:91047123 | AGCTCAGAGCTCCAA[A/G]ATCAGCTACTCGCAT | 11783 |
rs36468533 | snp | A/G | 0.21875 | 0.248039 | intron-variant | Apaf1 | Mm_Celera | 10:91013213 | AGAACACTGAGGAAA[A/G]CCGTAGCTATGCAAT | 11783 |
rs36476253 | snp | A/G | 0.197531 | 0.244432 | intron-variant | Apaf1 | Mm_Celera | 10:91032818 | AGCCACACAAGCAAC[A/G]GCCCCTGAAAGGATG | 11783 |
rs36489034 | snp | A/C | 0.18 | 0.24 | intron-variant | Apaf1 | Mm_Celera | 10:91063482 | GTAGCAGCGACACTC[A/C]GAGGCAGCCTAGCAC | 11783 |
rs36503066 | snp | A/G | 0.244898 | 0.249948 | missense | Apaf1 | Mm_Celera | 10:91060136 | ATTTCAACACTTATC[A/G]ACATGGCTTCATCTA | 11783 |
rs36520056 | snp | C/G | 0.473373 | 0.11227 | intron-variant | Apaf1 | Mm_Celera | 10:91039294 | GGCGGCCTGAGAATA[C/G]AGCTGACGGATCAGG | 11783 |
rs36524760 | snp | C/T | 0.231111 | 0.249285 | utr-variant-3-prime | Apaf1 | Mm_Celera | 10:90990108 | AATATGCATCAACAA[C/T]GGAAACAGCTTCACT | 11783 |
rs36548658 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Apaf1 | Mm_Celera | 10:91051413 | AAATCATTCTGTAAT[G/T]GTCTGGTCCAAGCTA | 11783 |
rs36560179 | snp | C/T | 0.375 | 0.216506 | intron-variant | Apaf1 | GRCm38.p3 | 10:91041479 | CATAAATATTATGGA[C/T]CTATAAATCCAGGTT | 11783 |
rs36590157 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Apaf1 | Mm_Celera | 10:90994390 | CATCTCTCCTCTATG[C/T]ACCATCCTCAGAGCT | 11783 |
rs36625003 | snp | A/G | 0.473373 | 0.11227 | intron-variant | Apaf1 | Mm_Celera | 10:91047216 | TCAGGTTAACCCTTA[A/G]CTCAGTAGTTCCGCT | 11783 |
rs36625166 | snp | A/T | 0.391111 | 0.206368 | intron-variant | Apaf1 | Mm_Celera | 10:90992391 | CCCAGGGCCACTGCA[A/T]GGCATTCCGGAGAAA | 11783 |
rs36628091 | snp | A/T | 0.336735 | 0.234472 | intron-variant | Apaf1 | Mm_Celera | 10:90994091 | TCAAAGCAGAAGGCA[A/T]AGCACTGATTGTCAC | 11783 |
rs36634439 | snp | G/T | 0.5 | 0 | intron-variant | Apaf1 | Mm_Celera | 10:91028009 | CTAGTTATTTAAGAC[G/T]GTGGCCTAGAAGGGA | 11783 |
rs36645962 | snp | A/C | 0.32 | 0.24 | intron-variant | Apaf1 | Mm_Celera | 10:91033487 | TGCCTGTGCACCCTA[A/C]GCTCTTGTGTGCTTT | 11783 |
rs36654766 | snp | C/G | 0.18 | 0.24 | synonymous-codon | Apaf1 | Mm_Celera | 10:91067176 | CTCTTCTTGGTCCAA[C/G]CGCATGCACAGATTC | 11783 |
rs36696181 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Apaf1 | Mm_Celera | 10:91032607 | ACATCTACCACAAGC[A/G]CAGAAGCAAACTGTA | 11783 |
rs36705464 | snp | A/G | 0.197531 | 0.244432 | intron-variant | Apaf1 | Mm_Celera | 10:91067374 | TCTTGAATTCTGGTA[A/G]GAGTTTATTACTGAG | 11783 |
rs36706094 | snp | C/T | 0.42 | 0.183303 | intron-variant | Apaf1 | Mm_Celera | 10:91033946 | AATCGGTGTGTCCAT[C/T]AGCTGAAGACCGGTA | 11783 |
rs36707004 | snp | C/T | 0.32 | 0.24 | intron-variant | Apaf1 | Mm_Celera | 10:90993130 | TAGGGAACCTGGGCT[C/T]CCGAGAGAATCAAGA | 11783 |
rs36719188 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Apaf1 | Mm_Celera | 10:91040118 | AGCTTCAGAAAGTTA[A/G]GCAGAGTCAGGTATT | 11783 |
rs36738165 | snp | A/G | 0.32 | 0.24 | intron-variant | Apaf1 | Mm_Celera | 10:90993729 | CTGCCTCTGAGTATA[A/G]AATGCCTTCATTACA | 11783 |
rs36739900 | snp | A/T | 0.5 | 0 | intron-variant | Apaf1 | Mm_Celera | 10:90991704 | ATTCTTTTTTTTTTT[A/T]ATGGACATGCAGATT | 11783 |
rs36747805 | snp | A/G | 0.5 | 0 | intron-variant | Apaf1 | Mm_Celera | 10:91041539 | TTCACTAATTTATCT[A/G]ATTTTCCCTTATTGT | 11783 |
rs36756937 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Apaf1 | Mm_Celera | 10:90996907 | TGAATGAGGTAGCTA[C/T]GAATACAGTGTGCAC | 11783 |
rs36757480 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Apaf1 | Mm_Celera | 10:90995113 | GAAGCCAACTTGTTA[A/G]AGACAACTGAAGAAG | 11783 |
rs36775144 | snp | A/G | 0.152778 | 0.230321 | utr-variant-3-prime | Apaf1 | Mm_Celera | 10:90990824 | TTCACAGACACTGAC[A/G]GCCAGAGTCCAGCTA | 11783 |
rs36783075 | snp | C/T | 0.46281 | 0.131194 | intron-variant | Apaf1 | Mm_Celera | 10:91021637 | CTGAGAACAACTTAT[C/T]ATAAAGCTCTGAAGC | 11783 |
rs36783307 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Apaf1 | Mm_Celera | 10:91001708 | GTTGAAGCAGTGCCA[A/G]CAACCGGGACAAAAT | 11783 |
rs36787631 | snp | C/T | 0.375 | 0.216506 | intron-variant | Apaf1 | Mm_Celera | 10:91009076 | TACAGAAGTGTTCCG[C/T]TGTTCCTCTCTCTAA | 11783 |
rs36808779 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Apaf1 | Mm_Celera | 10:90998434 | TAGCAGGGAGAATAA[A/G]GTGAAGGAGGTGCCC | 11783 |
rs36820190 | snp | C/G | 0.489796 | 0.070696 | intron-variant | Apaf1 | Mm_Celera | 10:91032762 | GAACTAACCAGCTCT[C/G]AGAAATGGACTATGA | 11783 |
rs36823877 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Apaf1 | Mm_Celera | 10:91001956 | TCTGTCACCAAGATA[C/T]AAACGACTGAAGAAA | 11783 |
rs36827649 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Apaf1 | Mm_Celera | 10:90992914 | ACGAGACTAGGTTTC[A/G]TATTTGTCTGTGCCC | 11783 |
rs36833174 | snp | C/T | 0.489796 | 0.070696 | intron-variant | Apaf1 | Mm_Celera | 10:91037806 | TGAGTGGTTTAGAAT[C/T]GCAGTATTTAATTAG | 11783 |
rs36862062 | snp | C/T | 0.124444 | 0.216185 | missense | Apaf1 | Mm_Celera | 10:91048199 | GTTTCTCTCCTGTCT[C/T]GGCTTTGAACACCTG | 11783 |
rs36876024 | snp | C/T | 0.486111 | 0.0821678 | intron-variant | Apaf1 | Mm_Celera | 10:91047479 | TAAACTTTCTTTGCA[C/T]GTCAAGCATTAATCT | 11783 |
rs36877631 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Apaf1 | Mm_Celera | 10:91001295 | TAATTAGCTTGATAC[A/G]GGGGACAAAATAAAA | 11783 |
rs36887559 | snp | C/T | 0.336735 | 0.234472 | utr-variant-3-prime | Apaf1 | Mm_Celera | 10:90990867 | CAGAGAGAAATCTCT[C/T]TAACACATGACTAGC | 11783 |
rs36889624 | snp | C/T | 0.5 | 0 | intron-variant | Apaf1 | Mm_Celera | 10:91037086 | TAAAAAGGCAGTGCT[C/T]GAGACTGGTGTGTCG | 11783 |
rs36891833 | snp | A/G | 0.32 | 0.24 | intron-variant | Apaf1 | Mm_Celera | 10:91047512 | AACTACCATTGTGCC[A/G]TTATTGCATTGTTTC | 11783 |
rs36895336 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Apaf1 | Mm_Celera | 10:91037845 | ATCAGTAAGTAATGT[A/T]TAAATTGCCTCCATA | 11783 |
rs36900471 | snp | A/C/T | 0.142012 | 0.225474 | intron-variant | Apaf1 | Mm_Celera | 10:91006310 | ATGAATTTAAGTTCG[A/C/T]GCCGTATACAATGTC | 11783 |
rs36952006 | snp | C/T | 0.152778 | 0.230321 | upstream-variant-2KB, intron-variant | Apaf1, Ikbip | Mm_Celera | 10:91083531 | ACTACTTCCCGTCCA[C/T]TCTGTAGCTTTGCGG | 11783 |
rs36955362 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Apaf1 | Mm_Celera | 10:91048328 | TTTTCAAAACAAAAA[C/T]GGAATGTAGCAAACT | 11783 |
rs36973717 | snp | A/G | 0.165289 | 0.235211 | intron-variant | Apaf1 | Mm_Celera | 10:90992275 | TTCTTAAACCAAGCA[A/G]TAAGCAAGAATGACA | 11783 |
rs36975102 | snp | G/T | 0.35503 | 0.226867 | intron-variant | Apaf1 | Mm_Celera | 10:91028212 | ACAGGGTAAAAGAAC[G/T]GGCAAATGTGAAACA | 11783 |
rs37000261 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Apaf1 | Mm_Celera | 10:91047009 | GTTGTTCCCCAAAGT[C/T]TCAAGCTTTCACTAT | 11783 |
rs37004040 | snp | A/G | 0.165289 | 0.235211 | intron-variant | Apaf1 | Mm_Celera | 10:91037607 | TTCCTTTTCATTTGA[A/G]CTGCTGGTTACAGAA | 11783 |
rs37009870 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Apaf1 | Mm_Celera | 10:90994312 | ATAGAAGCTCGGTGT[C/T]GTAGCTGGGCAGTTA | 11783 |
rs37036440 | snp | A/G | 0.142012 | 0.225474 | synonymous-codon | Apaf1 | Mm_Celera | 10:90999760 | TCTTTCTATTCTTCC[A/G]GTAATGACATTCCAC | 11783 |
rs37051775 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Apaf1 | Mm_Celera | 10:91049266 | TTCACTTCTAAACTA[C/T]CATCTTCCTAAATCT | 11783 |
rs37052080 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Apaf1 | Mm_Celera | 10:90996195 | CAAGTCCAAACTCTC[A/G]TATTTCTCTCCATTA | 11783 |
rs37058888 | snp | C/T | 0.18 | 0.24 | intron-variant | Apaf1 | Mm_Celera | 10:91021717 | ACAGGATGCGCATAA[C/T]CAGCTTCCATGTAAG | 11783 |
rs37062139 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Apaf1 | Mm_Celera | 10:91047325 | ATTTTATGCATTCTA[C/T]ACTTTCTTATCTATA | 11783 |
rs37064226 | snp | A/G | 0.132653 | 0.220748 | synonymous-codon | Apaf1 | Mm_Celera | 10:90991483 | AATATATAAAATACC[A/G]AGATTATCGACAGTC | 11783 |
rs37070444 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Apaf1 | Mm_Celera | 10:91023012 | ATCAAATTACATCAT[A/G]TGCCTGCATGAAAAT | 11783 |
rs37072555 | snp | A/G | 0.165289 | 0.235211 | upstream-variant-2KB, intron-variant | Apaf1, Ikbip | Mm_Celera | 10:91084598 | GTTCAACTGAAATAC[A/G]GATCATTGTCCTCTT | 11783 |
rs37091862 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Apaf1 | Mm_Celera | 10:90994570 | TCACACATTGAAAAC[A/G]CTCCCTCGATTATCT | 11783 |
rs37129948 | snp | C/G | 0.231111 | 0.249285 | upstream-variant-2KB, intron-variant | Apaf1, Ikbip | Mm_Celera | 10:91083616 | AATAAAAAAAAGTTC[C/G]TTGTTGCTGAGCGAT | 11783 |
rs37165047 | snp | A/G | 0.124444 | 0.216185 | synonymous-codon | Apaf1 | Mm_Celera | 10:91048206 | TCCTGTCTCGGCTTT[A/G]AACACCTGCGTAACA | 11783 |
rs37174047 | snp | G/T | 0.42 | 0.183303 | intron-variant | Apaf1 | Mm_Celera | 10:91047644 | CCATCTAGCTTCACA[G/T]AGTTCACCAGAGCAG | 11783 |
rs37184859 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Apaf1 | Mm_Celera | 10:90994164 | CTCAAGACACAGCCT[C/T]TACAGTGCTGCAGCA | 11783 |
rs37196484 | snp | C/T | 0.5 | 0 | upstream-variant-2KB, intron-variant | Apaf1, Ikbip | GRCm38.p3 | 10:91083480 | TTATTAAGCATCTAC[C/T]ACTGCACGTCACAAG | 11783 |
rs37196801 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Apaf1 | Mm_Celera | 10:91001902 | CAAACAAGGGCCTAC[C/T]GTGAACAGACCTGAG | 11783 |
rs37220604 | snp | C/T | 0.5 | 0 | intron-variant | Apaf1 | Mm_Celera | 10:91033452 | TGTATTCTGAGGAGG[C/T]CACTGCACCGTTCCC | 11783 |
rs37233416 | snp | A/G | 0.260355 | 0.249785 | synonymous-codon | Apaf1 | Mm_Celera | 10:91039809 | GAAATCATTTGACCC[A/G]GTGGCCAAGAGAAGG | 11783 |
rs37244953 | snp | C/G | 0.489796 | 0.070696 | intron-variant | Apaf1 | Mm_Celera | 10:91041062 | ATGAGAAAGCTTACA[C/G]TGAAGTGAGTCATGT | 11783 |
rs37272984 | snp | A/C | 0.493827 | 0.0552116 | intron-variant | Apaf1 | Mm_Celera | 10:91040009 | CTCACTGGGCAGACG[A/C]TATCTATCTCCTGTG | 11783 |
rs37320660 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Apaf1 | Mm_Celera | 10:90992363 | TGGTGATGACCTCAC[A/G]GCCAAGTCTGCACCC | 11783 |
rs37328382 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Apaf1 | Mm_Celera | 10:90998647 | ACCGAGTGAGTAAAG[A/G]CTGTCTGTTCGCATC | 11783 |
rs37334877 | snp | A/C | 0.165289 | 0.235211 | intron-variant | Apaf1 | Mm_Celera | 10:91031303 | TTCCTATGCTGTTTC[A/C]TACTGCGTGTCCTGG | 11783 |
rs37336660 | snp | A/G | 0.18 | 0.24 | intron-variant | Apaf1 | Mm_Celera | 10:91073495 | AAAAAACATTCCAAG[A/G]CTCTGAAGACTTTCA | 11783 |
rs37339322 | snp | C/T | 0.165289 | 0.235211 | intron-variant | Apaf1 | Mm_Celera | 10:90996875 | ACTCAGCACCTGACA[C/T]ACCTGTCTAACTGGG | 11783 |
rs37345001 | snp | A/G | 0.32 | 0.24 | intron-variant | Apaf1 | Mm_Celera | 10:90995394 | AGTAGTGAGTGCCAC[A/G]GTAGATGAAATTGGG | 11783 |
rs37357080 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Apaf1 | Mm_Celera | 10:91042956 | AGGAAACTTTTGACA[A/G]CTTAGCAATAAACTC | 11783 |
rs37359374 | snp | A/G | 0.197531 | 0.244432 | intron-variant | Apaf1 | Mm_Celera | 10:91018241 | GTGTGGACCTGCTAG[A/G]TGGCAACATCCCTCA | 11783 |
rs37375369 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Apaf1 | Mm_Celera | 10:91038697 | AAAATCTGAGATGCC[A/G]CTGTAAAAATGGTGT | 11783 |
rs37421000 | snp | A/G | 0.336735 | 0.234472 | utr-variant-3-prime | Apaf1 | Mm_Celera | 10:90990571 | CGTCACTGGCTGACT[A/G]ACACCTAAGCATGGA | 11783 |
rs37430346 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Apaf1 | Mm_Celera | 10:90994184 | GTGCTGCAGCAGATC[C/T]ATCCTGCTACGTTAT | 11783 |
rs37441432 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Apaf1 | Mm_Celera | 10:90994199 | CATCCTGCTACGTTA[C/T]TTCAAGGTTTGCCAA | 11783 |
rs37521001 | snp | A/C | 0.497041 | 0.0383476 | intron-variant | Apaf1 | Mm_Celera | 10:91038033 | GAATACAGGAACTAC[A/C]GCTCAGGTCAAACAG | 11783 |
rs37532831 | snp | A/C | 0.5 | 0 | intron-variant | Apaf1 | GRCm38.p3 | 10:91041443 | TTTAAAATATTACTT[A/C]TAATCAAAGATATCA | 11783 |
rs37560453 | snp | C/T | 0.165289 | 0.235211 | upstream-variant-2KB, intron-variant | Apaf1, Ikbip | Mm_Celera | 10:91084563 | GAGTACTGGGTTTTG[C/T]TATAAGTTAATAAAA | 11783 |
rs37569482 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Apaf1 | Mm_Celera | 10:91047150 | GCATTTTCCTGTGAC[A/G]CTCTAATGATAAATG | 11783 |
rs37587441 | snp | A/C | 0.21875 | 0.248039 | intron-variant | Apaf1 | Mm_Celera | 10:90999642 | TAGACACTTCACGTG[A/C]CTAACTGACCTTGGC | 11783 |
rs37597847 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Apaf1 | Mm_Celera | 10:90995321 | TTGCTGGTACTATTA[C/T]TATCAAGAAAGAAAA | 11783 |
rs37607190 | snp | A/T | 0.375 | 0.216506 | intron-variant | Apaf1 | Mm_Celera | 10:91039439 | CAAACACTGCGACAG[A/T]AAACCGGGAAGGAGC | 11783 |
rs37621303 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Apaf1 | Mm_Celera | 10:90997204 | ACCTCAGTCAGCACA[C/T]GCCTTACCCGGATTT | 11783 |
rs37625241 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Apaf1 | Mm_Celera | 10:90995912 | CTTAAAAACAAAAAG[A/G]AGAGTGTGCTGGATC | 11783 |
rs37637926 | snp | A/T | 0.124444 | 0.216185 | utr-variant-3-prime | Apaf1 | Mm_Celera | 10:90989650 | AAGACCAAGACTTTT[A/T]AAAAACTGACGGTTG | 11783 |
rs37662666 | snp | C/G | 0.165289 | 0.235211 | intron-variant | Apaf1 | Mm_Celera | 10:91008931 | TCAGGAAACTTCAGT[C/G]GGCTGCCTACTGTGT | 11783 |
rs37681785 | snp | C/G | 0.32 | 0.24 | intron-variant | Apaf1 | Mm_Celera | 10:91037720 | TCTCAGTCCACCAAG[C/G]AACTTGAAGGCCTCA | 11783 |
rs37690783 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Apaf1 | Mm_Celera | 10:91033391 | CTCAGCCCCTAGAAG[A/G]CAATGATAAAGTTTC | 11783 |
rs37723813 | snp | A/G | 0.277778 | 0.248452 | utr-variant-3-prime | Apaf1 | Mm_Celera | 10:90991262 | AAATAGAGTAAAAGT[A/G]TGTTCCTTTGTGGAG | 11783 |
rs37774776 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Apaf1 | Mm_Celera | 10:91034678 | ATAATTTTGTCACTG[C/T]TTATCCACTTGCCAT | 11783 |
rs37816064 | snp | A/G | 0.5 | 0 | intron-variant | Apaf1 | Mm_Celera | 10:91048911 | TATAAAAGTATGTGG[A/G]AAAAGCACTTCCCGC | 11783 |
rs37818890 | snp | C/G | 0.260355 | 0.249785 | utr-variant-3-prime | Apaf1 | Mm_Celera | 10:90989568 | TTCAAGGTCAGCCTC[C/G]AGAGCTGCTGCGTGT | 11783 |
rs37819893 | snp | A/G | 0.5 | 0 | intron-variant | Apaf1 | Mm_Celera | 10:91030272 | AGTTTCCTGCTAGAG[A/G]GACATAAGTCTACAA | 11783 |
rs37832540 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Apaf1 | Mm_Celera | 10:90995135 | CTGAAGAAGCACAAG[A/G]CCTGCTATGAGACTT | 11783 |
rs37839760 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Apaf1 | Mm_Celera | 10:90995629 | TGCTCTTTCTTTCAC[A/G]CCCTCGAGTAACGCT | 11783 |
rs37842562 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Apaf1 | Mm_Celera | 10:90997488 | CCAATCTCTAACCTG[C/T]AACCTTGTCAACTTT | 11783 |
rs37846967 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Apaf1 | Mm_Celera | 10:91049220 | TAATAGTCTAAAGGA[A/G]CGTCTACGAATGTGC | 11783 |
rs37862104 | snp | A/G | 0.391111 | 0.206368 | utr-variant-3-prime | Apaf1 | Mm_Celera | 10:90990495 | CGACTCTTGAAAGTC[A/G]TGGAGAGAACAGCAT | 11783 |
rs37863095 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Apaf1 | Mm_Celera | 10:90999584 | TCTTGCCTTATACAT[C/T]GTTTGGACTCATAAT | 11783 |
rs37872521 | snp | C/T | 0.444444 | 0.157135 | upstream-variant-2KB, intron-variant | Apaf1, Ikbip | Mm_Celera | 10:91083517 | CATACCTAAAAACCA[C/T]TACTTCCCGTCCACT | 11783 |
rs37907827 | snp | A/G | 0.277778 | 0.248452 | synonymous-codon | Apaf1 | Mm_Celera | 10:91048173 | ATCTTCGTGAGCTTT[A/G]ATGTCAAGAAGTTTC | 11783 |
rs37917106 | snp | A/C | 0.408163 | 0.193609 | intron-variant | Apaf1 | Mm_Celera | 10:91046944 | TGTATAATCATTGCC[A/C]AATCAAATTCAAAAG | 11783 |
rs37957104 | snp | A/G | 0.32 | 0.24 | utr-variant-3-prime | Apaf1 | Mm_Celera | 10:90989953 | ATCTAAAATCCACCT[A/G]AGGAAGGGCTGGTCG | 11783 |
rs37972209 | snp | A/G | 0.391111 | 0.206368 | utr-variant-3-prime | Apaf1 | Mm_Celera | 10:90990783 | AAACGAAACAACTAA[A/G]AGAGTGCAAGGTGGT | 11783 |
rs37990278 | snp | G/T | 0.375 | 0.216506 | synonymous-codon | Apaf1 | Mm_Celera | 10:90999679 | ATCAGCAGAGGTAGA[G/T]GAAAACTTGGTCGCA | 11783 |
rs38045397 | snp | C/T | 0.32 | 0.24 | intron-variant | Apaf1 | Mm_Celera | 10:91038537 | TATCCTTGTGGAAAG[C/T]TGTAAAACCGCATCT | 11783 |
rs38050150 | snp | C/G | 0.152778 | 0.230321 | intron-variant | Apaf1 | Mm_Celera | 10:90999199 | AATATGATACAGGTA[C/G]GAGTGGATCAGAGAG | 11783 |
rs38066435 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Apaf1 | Mm_Celera | 10:90996194 | GCAAGTCCAAACTCT[C/T]GTATTTCTCTCCATT | 11783 |
rs38074374 | snp | C/T | 0.495868 | 0.0452663 | intron-variant | Apaf1 | Mm_Celera | 10:91031770 | CCTCTAGAATTCCAA[C/T]TAGATTAAATGTCAT | 11783 |
rs38154487 | snp | G/T | 0.336735 | 0.234472 | intron-variant | Apaf1 | Mm_Celera | 10:90995953 | CAGTTTCCAAAGAAT[G/T]AAGAGAGAAGCGCAG | 11783 |
rs38189031 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Apaf1 | Mm_Celera | 10:91000473 | AATTACTGCACGATC[C/T]GAATGTTTTCTTTAA | 11783 |
rs38241400 | snp | C/T | 0.124444 | 0.216185 | missense | Apaf1 | Mm_Celera | 10:90995749 | CTTCCTCTACCGAGA[C/T]CGGAGCACACGAATG | 11783 |
rs38264568 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Apaf1 | Mm_Celera | 10:91001719 | GCCAACAACCGGGAC[A/G]AAATAACAAACACCA | 11783 |
rs38445462 | snp | C/T | 0.391111 | 0.206368 | synonymous-codon | Apaf1 | Mm_Celera | 10:90991451 | AACGCTTAGCCATTT[C/T]ACTCTAAAACCTGTA | 11783 |
rs38494044 | snp | C/T | 0.46281 | 0.131194 | intron-variant | Apaf1 | Mm_Celera | 10:91039330 | CACCAGCGGGATCCA[C/T]GCTCCCTGTGCAGTT | 11783 |
rs38507780 | snp | A/C | 0.32 | 0.24 | intron-variant | Apaf1 | Mm_Celera | 10:91048290 | GAAATACATCTCAGC[A/C]AGTTCTTACTTAGTC | 11783 |
rs38551445 | snp | A/G | 0.489796 | 0.070696 | intron-variant | Apaf1 | Mm_Celera | 10:91047380 | ACTCTCAGATATTGG[A/G]CAAAACTCATTTCAT | 11783 |
rs38581795 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Apaf1 | Mm_Celera | 10:90995429 | GTAGGTTCAGCTGGG[A/C]GAAGAGAGCTCTCAC | 11783 |
rs38682545 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Apaf1 | Mm_Celera | 10:91022965 | GTCTAGACCACTTTC[A/G]AGATAGCACATGTCT | 11783 |
rs38731001 | snp | G/T | 0.495868 | 0.0452663 | intron-variant | Apaf1 | Mm_Celera | 10:91031282 | TCTGCTCCTGTGGTG[G/T]CGGCTTTCCTATGCT | 11783 |
rs38784792 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Apaf1 | Mm_Celera | 10:90992477 | GGAGTGGGCACATGA[C/T]TGCTTCTCTTCACTA | 11783 |
rs38880948 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Apaf1 | Mm_Celera | 10:91043024 | CAACTTCCTAAAGTT[A/G]GGCCTAAATCAGGCC | 11783 |
rs38884870 | snp | A/G | 0.396694 | 0.202437 | intron-variant | Apaf1 | Mm_Celera | 10:91047250 | TTTCTGCTTCTGCAC[A/G]TTGCACACAATGACT | 11783 |
rs38989018 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Apaf1 | Mm_Celera | 10:91039445 | CTGCGACAGTAAACC[A/G]GGAAGGAGCTGGAGA | 11783 |
rs39041307 | snp | A/T | 0.375 | 0.216506 | intron-variant | Apaf1 | Mm_Celera | 10:91047719 | CACACCAAGGCCAAC[A/T]GAAAAGCAGCCATGC | 11783 |
rs39079058 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Apaf1 | Mm_Celera | 10:91048452 | CTACACAGAAGTGAT[A/G]AAACACAGCTTCATC | 11783 |
rs39215123 | snp | G/T | 0.21875 | 0.248039 | intron-variant | Apaf1 | Mm_Celera | 10:91021854 | CGCTTACGACAACCT[G/T]TCGGAGCCGGCCACC | 11783 |
rs39344314 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Apaf1 | Mm_Celera | 10:91002185 | CCCCAAGGTAACAAG[A/G]GAGTTGATCGGGATA | 11783 |
rs39344357 | snp | A/G | 0.35503 | 0.226867 | intron-variant | Apaf1 | Mm_Celera | 10:90992282 | ACCAAGCAGTAAGCA[A/G]GAATGACAGTTGAGC | 11783 |
rs39345271 | snp | A/C | 0.142012 | 0.225474 | missense | Apaf1 | Mm_Celera | 10:90999693 | ATGAAAACTTGGTCG[A/C]ATCAGAAGAGATAGC | 11783 |
rs39458316 | snp | A/G | 0.375 | 0.216506 | synonymous-codon | Apaf1 | Mm_Celera | 10:91048149 | GGAGAACGCGCAGCA[A/G]AGCACCTCATCTTCG | 11783 |
rs39488313 | snp | C/T | 0.426035 | 0.177515 | intron-variant | Apaf1 | Mm_Celera | 10:90998095 | GAAGTAGACATAGAC[C/T]CTTTCCTTGACATTT | 11783 |
rs39514077 | snp | G/T | 0.336735 | 0.234472 | intron-variant | Apaf1 | Mm_Celera | 10:91049243 | GAATGTGCAAGAGTT[G/T]ACATTTCTTCACTTC | 11783 |
rs39592559 | snp | A/T | 0.48 | 0.0979796 | intron-variant | Apaf1 | Mm_Celera | 10:91048287 | ATGGAAATACATCTC[A/T]GCAAGTTCTTACTTA | 11783 |
rs39656630 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Apaf1 | Mm_Celera | 10:91005403 | ATTCACTAAACCTAT[A/G]TCTCAGGCTGGTGAT | 11783 |
rs39659422 | snp | A/G | 0.345679 | 0.230967 | intron-variant | Apaf1 | Mm_Celera | 10:91033526 | ATCTTTAAAGAAAAC[A/G]CTTTAAGACCATTTC | 11783 |
rs39907659 | snp | C/T | 0.375 | 0.216506 | intron-variant | Apaf1 | Mm_Celera | 10:91020233 | CATATACATGTATCT[C/T]AGCCACATCATGAAG | 11783 |
rs45640212 | snp | C/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91049020 | GGCCTCTGACAATTT[C/G]TTTAACCAATGGTTT | 11783 |
rs45659175 | snp | C/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91032106 | TCCCAGGTTAGGGTG[C/G]TACCCAAGAGGGGCT | 11783 |
rs45660057 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91038862 | TATAATTCCTAATCA[C/T]AATATCATCAGATAT | 11783 |
rs45661201 | snp | A/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91048533 | TTTATATGAGTACAC[A/T]GCAGCTGCCTTCAGA | 11783 |
rs45666712 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91048746 | ATTAAGGCTGCAGAT[A/G]TAGTTCAGGGGTTGC | 11783 |
rs45698908 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91047686 | AGTAGGAAAGTCAGA[C/T]AGCATGGAATAACTA | 11783 |
rs45723656 | snp | A/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91041366 | AAATCAGTCTATAAA[A/T]CTAAAATAGAATCAG | 11783 |
rs45731248 | snp | A/T | | | upstream-variant-2KB, intron-variant | Apaf1, Ikbip | Mm_Celera | 10:91084292 | TCCTCCAGGGTAGAG[A/T]AGTTTTGATGCAGGT | 11783 |
rs45733572 | snp | A/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91048499 | ACAAAGTTTTTTTTT[A/T]AAGATTTATTTATTT | 11783 |
rs45818509 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91032451 | CTACATGAGAGCTCA[C/T]CTCAAAAGGAAAAAA | 11783 |
rs45847789 | snp | C/T | | | upstream-variant-2KB, missense | Apaf1, Ikbip | Mm_Celera | 10:91083278 | TGCTGTCTCTGGCGA[C/T]GACCCTGGGCCTGGC | 11783 |
rs45869663 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91080561 | TTTTACTGTAATACT[C/T]AAGTCCTGGTGCTTT | 11783 |
rs45875569 | snp | G/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91038893 | TCATGAGGCGGACAC[G/T]TGGGTTTTGCTTATA | 11783 |
rs45893662 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91045263 | CATAAGTGGCCCTAA[A/G]AATTCTACAGGGAAC | 11783 |
rs45897185 | snp | C/G | | | upstream-variant-2KB, intron-variant | Apaf1, Ikbip | Mm_Celera | 10:91083479 | TTTATTAAGCATCTA[C/G]TACTGCACGTCACAA | 11783 |
rs45909910 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:90999271 | TCCCAGCCTGTAAAA[A/G]GTTCATGTGGTGGCC | 11783 |
rs46002505 | snp | G/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91042606 | TCACTAGTAACTTAG[G/T]TATGGCTTTAACCCT | 11783 |
rs46012245 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91039691 | CAAAACAAAACAAAA[C/T]AAAACAAAACCTAAT | 11783 |
rs46077467 | snp | A/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91052892 | CTCTCCTGCCCTGTA[A/T]GCAGCCTTTCTTTAA | 11783 |
rs46103775 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91039973 | CTACGTCCACAGGGA[A/G]AATAGGAAGAGCAAA | 11783 |
rs46123722 | snp | A/C | | | intron-variant | Apaf1 | Mm_Celera | 10:91032611 | CTACCACAAGCGCAG[A/C]AGCAAACTGTACTGG | 11783 |
rs46132472 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91038106 | AGCAAGTAACTCTAC[C/T]TGTCTAGTAACCCAA | 11783 |
rs46144840 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91031054 | GGCAGTGAGAAGCAA[C/T]GGCTGCTCTTCTAGA | 11783 |
rs46169336 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91062464 | TGCATTTACATGCTT[C/T]GTCCCCAGTTGATGA | 11783 |
rs46178281 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91038802 | ACCAGAGAATTTAAT[C/T]TACCTACAGTTATCT | 11783 |
rs46233328 | snp | C/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91000165 | TCTCTCCAGTTCTAG[C/G]AGATTCAGTGCTTTT | 11783 |
rs46302873 | snp | A/C | | | intron-variant | Apaf1 | Mm_Celera | 10:91042618 | TAGTTATGGCTTTAA[A/C]CCTTCAGTGAGCCAG | 11783 |
rs46322754 | snp | C/G/T | | | intron-variant | Apaf1 | GRCm38.p3 | 10:91041585 | AGCTAATCAACCTAA[C/G/T]CATTTTTTTTTCTTT | 11783 |
rs46331039 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91048390 | AAGTGTTTATTTATG[C/T]AAGCATAAACAGAGA | 11783 |
rs46393043 | snp | G/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91031372 | TTTTCTTACGAGGCC[G/T]CCCATATCCCCAGAG | 11783 |
rs46397567 | snp | A/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91062275 | ACACTTATTTTGCAC[A/T]TCCTTTAAAAACCAT | 11783 |
rs46495586 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91045341 | TTACAAAAATCAGTA[A/G]TCCTCCCATATACAA | 11783 |
rs46539340 | snp | A/C | | | upstream-variant-2KB, utr-variant-5-prime | Apaf1, Ikbip | Mm_Celera | 10:91083119 | TCAAGATCTTCAGGG[A/C]TCCAGACATGTCCGA | 11783 |
rs46566427 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91032550 | AGGGACTCACAGCTG[C/T]CTGCTGCTGCCCTCT | 11783 |
rs46570012 | snp | A/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91047606 | CTCAATTCTTAATTG[A/T]TTAGGAATCATTACA | 11783 |
rs46639781 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91028935 | GCCAAGAAGTGGGGA[A/G]AGTCAGGGGCCTGTA | 11783 |
rs46712072 | snp | A/G | | | upstream-variant-2KB, intron-variant | Apaf1, Ikbip | Mm_Celera | 10:91083400 | TTTAACAATGTTCTG[A/G]TAGCATGCTCCTGTC | 11783 |
rs46757511 | snp | A/C | | | intron-variant | Apaf1 | Mm_Celera | 10:91000280 | ACATAGCCCCCCCCC[A/C]AAAAAAACCAAGTTT | 11783 |
rs46794363 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91028746 | ATACCCTGCTAGCAG[A/G]AATGTAAAATGGTGC | 11783 |
rs46847874 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91048592 | ATGGTTGTGAGCCAC[C/T]GTGTGGTTGCTGGGA | 11783 |
rs46862198 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91048569 | ACCAGAAGAGTGCAT[C/T]GTTACAGATGGTTGT | 11783 |
rs46888228 | snp | A/G | | | upstream-variant-2KB, intron-variant | Apaf1, Ikbip | Mm_Celera | 10:91083516 | ACATACCTAAAAACC[A/G]CTACTTCCCGTCCAC | 11783 |
rs46890332 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91043460 | AAGGATAAACATTAC[C/T]TCAGGGTAAAGGGAT | 11783 |
rs46943045 | snp | A/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91047592 | CTGTGCCCCTGTGCC[A/T]CAATTCTTAATTGAT | 11783 |
rs46973659 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91044257 | AAGAGTTGGTTCCTC[A/G]AGAAAATAAATAAGA | 11783 |
rs47007944 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91038853 | GCAATCTCCTATAAT[C/T]CCTAATCACAATATC | 11783 |
rs47012285 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91000536 | CATGCCTTAAGTCCC[A/G]GAAACTCAGGAGGCA | 11783 |
rs47032798 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91040875 | GGAAATGACTATGTA[A/G]TTAATATACACTAAT | 11783 |
rs47046345 | snp | A/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91030974 | TTTTAAAAACTTTTT[A/T]AAGTGATGAAGAAAG | 11783 |
rs47052246 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91048956 | CAGTGAGAACAGAAG[C/T]AGCCTTTGGAAGCCG | 11783 |
rs47070152 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91029574 | TGATTACAATGCCAA[C/T]TGTGTACATTTAAGA | 11783 |
rs47100614 | snp | C/T | | | intron-variant | Apaf1 | GRCm38.p3 | 10:91043874 | GAGAGAGAGAAATGA[C/T]TCCCTACACTATTAG | 11783 |
rs47127557 | snp | A/C | | | intron-variant | Apaf1 | Mm_Celera | 10:91062033 | TTTCTGAGTTCGAGG[A/C]CAGCCTGGGATACAC | 11783 |
rs47152335 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91062015 | GAGGCAGAGGCAGGC[A/G]GATTTCTGAGTTCGA | 11783 |
rs47206538 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91039063 | GGCACTGCACTTACG[A/G]AACAATGAGTCTGAA | 11783 |
rs47221853 | snp | A/G | | | intron-variant, upstream-variant-2KB | Apaf1, Ikbip | GRCm38.p3 | 10:91081810 | TGCCTCCCGAGTGCT[A/G]GGATTAAAGGCGTGC | 11783 |
rs47324792 | snp | A/C | | | intron-variant | Apaf1 | Mm_Celera | 10:91043885 | ATGACTCCCTACACT[A/C]TTAGACCATTATGAA | 11783 |
rs47332981 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91052119 | CCAGGCAACCAAGGG[C/T]AAGAATCCTATTCTA | 11783 |
rs47338146 | snp | A/G | | | intron-variant | Apaf1 | GRCm38.p3 | 10:91034604 | CAGAAATCTACATAT[A/G]CACATAACTTTAAAA | 11783 |
rs47406451 | snp | A/C | | | intron-variant | Apaf1 | Mm_Celera | 10:91062367 | TCAGGGTAGCAAAGG[A/C]GAGATTATAGTTTCA | 11783 |
rs47448493 | snp | A/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91043887 | GACTCCCTACACTAT[A/T]AGACCATTATGAATT | 11783 |
rs47473679 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91042065 | GAGGCAGAGGCAGGT[A/G]GATTTCTGAGTTTGA | 11783 |
rs47484989 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91048593 | TGGTTGTGAGCCACT[A/G]TGTGGTTGCTGGGAA | 11783 |
rs47505473 | snp | A/C | | | intron-variant | Apaf1 | Mm_Celera | 10:91063978 | AGCTCCTAATAGAAA[A/C]TTGGTTACAGTTTCA | 11783 |
rs47521963 | snp | A/G | | | intron-variant | Apaf1 | GRCm38.p3 | 10:91048632 | TGAACCTCTGGAAGA[A/G]CAGTCAGTGCTCTTA | 11783 |
rs47536264 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91029669 | CAAATTTCTGAGTTC[A/G]AAGCCAGCCTGGTCT | 11783 |
rs47586675 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91080605 | TTTATCCAACCTATA[A/G]ACCAAGTAGCGTTGC | 11783 |
rs47635462 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91080569 | TAATACTCAAGTCCT[A/G]GTGCTTTAAAGCGTG | 11783 |
rs47678147 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91029614 | GCCCGGCAGTAGTAG[C/T]GCATGCCTTTAGTCC | 11783 |
rs47734843 | snp | A/G/T | | | intron-variant | Apaf1 | GRCm38.p3 | 10:91043277 | CACTCTTCCCCCTCC[A/G/T]ATGCCTCAAGAAAAA | 11783 |
rs47750332 | snp | A/T | | | intron-variant | Apaf1 | GRCm38.p3 | 10:91041431 | AATTATATCATTTTT[A/T]AAATATTACTTATAA | 11783 |
rs47775977 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91047306 | TTAGTTTTACTAATA[C/T]ATAATTTTATGCATT | 11783 |
rs47833107 | snp | A/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91000529 | TGATGCACATGCCTT[A/T]AGTCCCAGAAACTCA | 11783 |
rs47835102 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91077802 | TAATCTTCCCATGAA[C/T]CCCAGGCTTAGCCTC | 11783 |
rs47837353 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91038597 | TTGCTATATAGCTCA[A/G]GCTCCTCCTGCCTCG | 11783 |
rs47853265 | snp | A/C/G | | | intron-variant | Apaf1 | GRCm38.p3 | 10:91034301 | CTCAGTCTCTGGAAC[A/C/G]CACCATGGTAGAAGC | 11783 |
rs47869896 | snp | G/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91081026 | AGAGTAATATACAGA[G/T]CGCCGAAGAAGGGCA | 11783 |
rs47932146 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91000518 | GCTGGGTATGGTGAT[A/G]CACATGCCTTAAGTC | 11783 |
rs48002235 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91000592 | AGCCTGATCTACATA[C/T]CAAGTTCCAGACCAA | 11783 |
rs48022257 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91038886 | CAGATATTCATGAGG[C/T]GGACACGTGGGTTTT | 11783 |
rs48025562 | snp | C/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91046034 | GATATCCTGAACGCA[C/G]TGACACGGAAGAAGA | 11783 |
rs48028625 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91034281 | CTCGAGCCCGCTGGC[C/T]GGAGCTCAGTCTCTG | 11783 |
rs48033576 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91032084 | TTCCCCCCCCCCCCC[A/G]CCCATGTCCCAGGTT | 11783 |
rs48041677 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91042529 | TAAAAAGGGAACTAA[C/T]GGTTTATTATAGGTG | 11783 |
rs48056855 | snp | G/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91045486 | AAAAACTTGAAGGAA[G/T]AAGTAGAAAAGATAT | 11783 |
rs48084373 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91080436 | TGGCTTTCTTCCTTC[A/G]TAATTTTATAAAGTG | 11783 |
rs48114022 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91048024 | GTTGTGAGCAGCCAT[A/G]CGGGTGCTCTGCAAG | 11783 |
rs48127230 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91041166 | ACACACACATACAAA[A/G]TCTATCTATCTATCT | 11783 |
rs48138393 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91041403 | TTTGATAAATTATAT[A/G]CTTTACAATTAGAAT | 11783 |
rs48139831 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91033293 | ACAGTTAGTAGGACA[A/G]ACTTAGGTTTGGGAA | 11783 |
rs48152095 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91034598 | CATGCACAGAAATCT[A/G]CATATACACATAACT | 11783 |
rs48208950 | snp | A/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91048617 | CTGGGAAATGAACTC[A/T]GAACCTCTGGAAGAA | 11783 |
rs48215560 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91047926 | AGTGAGTATTTTGCC[C/T]GAATGTATGTGTGCG | 11783 |
rs48217739 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91034432 | AGTGTAACTTAAAAA[A/G]GGGAACCTGGCATCA | 11783 |
rs48275050 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91080897 | GTGTGAATGTCTTAA[A/G]TATGCATAATCATTC | 11783 |
rs48301963 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91037716 | AACATCTCAGTCCAC[C/T]AAGGAACTTGAAGGC | 11783 |
rs48309668 | snp | A/G | | | synonymous-codon | Apaf1 | Mm_Celera | 10:91048164 | AAGCACCTCATCTTC[A/G]TGAGCTTTGATGTCA | 11783 |
rs48341169 | snp | G/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91031956 | TGGGTCCCCTAACCA[G/T]CAGATCAGGGCCTCA | 11783 |
rs48354400 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91039718 | TAATACAATACACAG[A/G]AGAAAATCAACGAAG | 11783 |
rs48359979 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91046461 | AAGATCAATAACACA[A/G]GTGACAGCTCACACT | 11783 |
rs48419251 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91028854 | GAGTATATAACATGG[C/T]TATTAAAAGTTGGGC | 11783 |
rs48455839 | snp | C/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91039061 | TTGGCACTGCACTTA[C/G]GGAACAATGAGTCTG | 11783 |
rs48511042 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91047953 | TGCGCCAGGAACATT[C/T]GGTGTTGACAGGGGT | 11783 |
rs48594774 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91000757 | AACTGCTCTTCAAGA[A/G]AACCTAGGTTCAGTT | 11783 |
rs48612359 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91034580 | CAGGCACAGTCAGTC[A/G]GTCATGCACAGAAAT | 11783 |
rs48679823 | snp | G/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91052939 | GGCTGAAGAGCTGAG[G/T]CAGCAGTTAAGAGCA | 11783 |
rs48709904 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91033407 | CAATGATAAAGTTTC[A/G]CACATCAGGAGATGA | 11783 |
rs48728060 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91043311 | ACAAGAAAGAAGACC[C/T]CTGTGGGGGCTGGCC | 11783 |
rs48757105 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91041908 | TATTATATAATCTGC[A/G]ACAGGGTCGCCCTTA | 11783 |
rs48778689 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91061494 | TTCTCATTAACATAG[C/T]CTTTAACATATGGTG | 11783 |
rs48845262 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91031961 | CCCCTAACCAGCAGA[C/T]CAGGGCCTCAGTCTC | 11783 |
rs48847601 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91047714 | CTATGCACACCAAGG[C/T]CAACTGAAAAGCAGC | 11783 |
rs48847996 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91031519 | GTCCGAGTGGAGTGG[A/G]TTGAGATGGCAGGAC | 11783 |
rs48899673 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91048450 | CACTACACAGAAGTG[A/G]TAAAACACAGCTTCA | 11783 |
rs48908445 | snp | A/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91028636 | CACCTCACACCTACT[A/T]CAATGGCTATACACT | 11783 |
rs48912056 | snp | A/C | | | intron-variant | Apaf1 | Mm_Celera | 10:91041030 | CATTTACCCAGATTC[A/C]CTGCTCTACACCTCT | 11783 |
rs48944985 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91049005 | AGTCACAAATCTCTC[A/G]GCCTCTGACAATTTG | 11783 |
rs49004007 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91080421 | CTGATAGCAAGATTC[C/T]GGCTTTCTTCCTTCA | 11783 |
rs49007749 | snp | C/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91075063 | ACATACCAAGTGGCT[C/G]AAGTGGCTCATTTAT | 11783 |
rs49024972 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91045348 | AATCAGTAGTCCTCC[C/T]ATATACAAATGACAA | 11783 |
rs49029045 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91039085 | GAGTCTGAACTAAAC[A/G]GGGTAATGAGGGACT | 11783 |
rs49032438 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91029612 | GGGCCCGGCAGTAGT[A/G]GCGCATGCCTTTAGT | 11783 |
rs49059205 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91032768 | ACCAGCTCTGAGAAA[C/T]GGACTATGAAACACT | 11783 |
rs49068773 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91041177 | CAAAATCTATCTATC[C/T]ATCTATCTAAATTCC | 11783 |
rs49071707 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91038838 | AAGAGACTAAAAGAT[A/G]CAATCTCCTATAATT | 11783 |
rs49074892 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91048286 | AATGGAAATACATCT[C/T]AGCAAGTTCTTACTT | 11783 |
rs49137799 | snp | A/C | | | intron-variant | Apaf1 | Mm_Celera | 10:91047650 | AGCTTCACATAGTTC[A/C]CCAGAGCAGGAGGAG | 11783 |
rs49153336 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91034412 | AGACAGACAGAAAGA[C/T]AGGTAGTGTAACTTA | 11783 |
rs49155817 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91043585 | ATCAGAAGAAATAGG[A/G]GAGGACACTATATAC | 11783 |
rs49163750 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91039090 | TGAACTAAACGGGGT[A/G]ATGAGGGACTTCTCT | 11783 |
rs49167962 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91047337 | CTACACTTTCTTATC[C/T]ATACATATCCAAAAG | 11783 |
rs49234327 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91080976 | AGAGATAATCAGAAG[A/G]TGACTGTCCTACGTG | 11783 |
rs49326926 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91043082 | GAGACAGTACAGAGG[C/T]TATTTACTTAACCAC | 11783 |
rs49332803 | snp | C/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91062029 | CAGATTTCTGAGTTC[C/G]AGGCCAGCCTGGGAT | 11783 |
rs49335712 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91032675 | AGACCCCTAAAGGAG[A/G]AACTATACTGAAAGC | 11783 |
rs49358646 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91042078 | GTGGATTTCTGAGTT[C/T]GAGGCCAGCCTGGTC | 11783 |
rs49402752 | snp | A/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91000523 | GTATGGTGATGCACA[A/T]GCCTTAAGTCCCAGA | 11783 |
rs49425986 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91047587 | CTGTGCTGTGCCCCT[A/G]TGCCTCAATTCTTAA | 11783 |
rs49524318 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91031366 | ATGACCTTTTCTTAC[A/G]AGGCCGCCCATATCC | 11783 |
rs49604085 | snp | C/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91040055 | CCTCTGAGCATGACA[C/G]TAACGTGAACCCACT | 11783 |
rs49604545 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91041644 | TGGATTTGGGACTCT[A/G]GCCAGAGAACCAGGT | 11783 |
rs49614696 | snp | A/C | | | intron-variant | Apaf1 | Mm_Celera | 10:91040957 | CTAGACATCCCACAG[A/C]CCTCTTCAGGGCTAA | 11783 |
rs49623652 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91031745 | AAAATTGCTTTACTC[C/T]CAACACACTCCTCTA | 11783 |
rs49711771 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91031901 | CCCTCCCCACCCGCC[A/G]CCGCCACATTTGCTG | 11783 |
rs49718016 | snp | A/T | | | intron-variant | Apaf1 | GRCm38.p3 | 10:91033424 | ACATCAGGAGATGAC[A/T]CAGCCACACCACTGT | 11783 |
rs49752149 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91031453 | AGAGCTAAGCTGGAC[A/G]GGAGGGGGGGGGACA | 11783 |
rs49755889 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91048944 | TTCCCAAAATCACAG[C/T]GAGAACAGAAGTAGC | 11783 |
rs49768583 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91061686 | CAACACCCCAGACCC[A/G]GGCAGCACTACCTTT | 11783 |
rs49774854 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91028623 | TAAATGAAGCCACCA[C/T]CTCACACCTACTACA | 11783 |
rs49790051 | snp | A/C | | | intron-variant | Apaf1 | Mm_Celera | 10:91046430 | TAGATTCCATTTGAC[A/C]CCTGTCGGAAAGGCC | 11783 |
rs49851962 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91041339 | TTCATGTCTAGTTTG[C/T]ACTGATTATATAAAT | 11783 |
rs49942355 | snp | C/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91039617 | TTTGAAGCTGGCCTG[C/G]TCTACAGAGTGAGTT | 11783 |
rs49999712 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91080582 | CTGGTGCTTTAAAGC[A/G]TGTTTCCTTTATCCA | 11783 |
rs50006385 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91041706 | gtccccaagatccaa[C/T]cccccagtttcacat | 11783 |
rs50014719 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:90999115 | CCTATATACTGCAGG[A/G]ACAATGACAGCTATG | 11783 |
rs50072272 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91044276 | AAATAAATAAGATCA[A/G]CAAACACTAATTCAA | 11783 |
rs50087602 | snp | C/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91034268 | GAGCAGGTAAGACCT[C/G]GAGCCCGCTGGCTGG | 11783 |
rs50102515 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91041367 | AATCAGTCTATAAAA[C/T]TAAAATAGAATCAGG | 11783 |
rs50118273 | snp | C/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91031857 | TTTAAATTAAGAAAT[C/G]CAGCTTCCTGCAAGA | 11783 |
rs50119558 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91040247 | GCAGCCAGGGCTACA[C/T]ACTAGGACCCCCTTC | 11783 |
rs50129199 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91063949 | TGCTTTCTTTTATAA[A/G]AGTTGCCTAAAAGAG | 11783 |
rs50167828 | snp | A/G/T | | | intron-variant | Apaf1 | GRCm38.p3 | 10:91032566 | CTGCTGCTGCCCTCT[A/G/T]CTGGGACAAGCAGGA | 11783 |
rs50168020 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91039410 | TGGATATGGAATTTA[A/G]AACGGGGACATCTCA | 11783 |
rs50175011 | snp | A/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91080495 | TTTTTTTATAGTAAA[A/T]TTTTTTACAGTAAAA | 11783 |
rs50178900 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91061664 | CACCAGAGCGTCAGC[A/G]TTCCCACAACACCCC | 11783 |
rs50228616 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91054087 | CCTTCAGATGAAGAT[A/G]TAGAACTCTCAGCTC | 11783 |
rs50229488 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91039962 | ACGGCTGTCCACTAC[A/G]TCCACAGGGAGAATA | 11783 |
rs50323617 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91000125 | TGTGGTTTGCAGCAC[C/T]TACACAAGGTGGCTC | 11783 |
rs50392725 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91030238 | CACACTTAAGACAAA[C/T]GGACATATTTTTCAT | 11783 |
rs50397856 | snp | A/G | | | intron-variant | Apaf1 | GRCm38.p3 | 10:91030171 | AAAATCGAATTTTGA[A/G]TCTTCAAATTTTACA | 11783 |
rs50400650 | snp | C/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91038219 | TCTGAATCTAATAAA[C/G]CTATGGGTCTGAGAC | 11783 |
rs50424916 | snp | G/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91037637 | ACGATAATTAATTCA[G/T]AGTAACATGAAGTTG | 11783 |
rs50435924 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91080663 | AGCCGCAGATCTTCA[C/T]TAGTAAGCACATATT | 11783 |
rs50510256 | snp | A/G | | | upstream-variant-2KB, intron-variant | Apaf1, Ikbip | GRCm38.p3 | 10:91084293 | CCTCCAGGGTAGAGT[A/G]GTTTTGATGCAGGTT | 11783 |
rs50523825 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91037721 | CTCAGTCCACCAAGG[A/G]ACTTGAAGGCCTCAC | 11783 |
rs50526187 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91039508 | ATGGGTTAATCCCTA[A/G]CAGTGAGGTTAAAAT | 11783 |
rs50534441 | snp | C/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91031455 | AGCTAAGCTGGACGG[C/G]AGGGGGGGGGACAGG | 11783 |
rs50534821 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91039514 | TAATCCCTAACAGTG[A/G]GGTTAAAATAAATAA | 11783 |
rs50544878 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91041026 | ACTCCATTTACCCAG[A/G]TTCCCTGCTCTACAC | 11783 |
rs50582803 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91079667 | GAATAATGTAAGAAC[A/G]AACAGGCGAATATGT | 11783 |
rs50595735 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:90998866 | AAGTGAGTGCTAACC[A/G]GCATCCTCCAACAGC | 11783 |
rs50601852 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91078657 | TGCTGTACTGTGGAT[A/G]TATATGAAGCAGAGT | 11783 |
rs50613909 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91032398 | GCTAGTGCTTTGCAG[C/T]TGAGGCAGGAGGATC | 11783 |
rs50617218 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91043359 | TCAGCGGTCCCAATT[C/T]CCCCAATAAAAAGAC | 11783 |
rs50621593 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91030976 | TTAAAAACTTTTTTA[A/G]GTGATGAAGAAAGTA | 11783 |
rs50645401 | snp | C/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91043329 | GTGGGGGCTGGCCCC[C/G]GACAGATCTCAGTAT | 11783 |
rs50670297 | snp | A/G | | | intron-variant | Apaf1 | GRCm38.p3 | 10:91028533 | GCCTGGGCCTAGCAC[A/G]GGGTTCAACTCCCAG | 11783 |
rs50696945 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91040994 | CTGAAAGAAACCCAA[A/G]CCAACCTTGCTTGCC | 11783 |
rs50749697 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91047715 | TATGCACACCAAGGC[C/T]AACTGAAAAGCAGCC | 11783 |
rs50793868 | snp | C/T | | | intron-variant | Apaf1 | GRCm38.p3 | 10:91041643 | ATGGATTTGGGACTC[C/T]GGCCAGAGAACCAGG | 11783 |
rs50849203 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91032772 | GCTCTGAGAAATGGA[C/T]TATGAAACACTCTAA | 11783 |
rs50875729 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91047690 | GGAAAGTCAGATAGC[A/G]TGGAATAACTATGCA | 11783 |
rs50882911 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91043630 | ATGCACACAAAAAAA[C/T]TTCAACTCTTAACAT | 11783 |
rs50910536 | snp | A/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91047323 | TAATTTTATGCATTC[A/T]ACACTTTCTTATCTA | 11783 |
rs50918451 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91041381 | ACTAAAATAGAATCA[A/G]GCTATATTTGATAAA | 11783 |
rs50947694 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91029327 | ATATGCCTTTAATCC[C/T]GGCACTCAGGAGGCA | 11783 |
rs50995565 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91039434 | CATCTCAAACACTGC[A/G]ACAGTAAACCGGGAA | 11783 |
rs51005876 | snp | G/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91031125 | AAGCATCTGTATGTA[G/T]AGTTCCAGGGGATCC | 11783 |
rs51022195 | snp | A/G | | | intron-variant | Apaf1 | GRCm38.p3 | 10:91033419 | TTCACACATCAGGAG[A/G]TGACACAGCCACACC | 11783 |
rs51037694 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91043487 | GGATAAAAGGGAAAA[C/T]GATATTCCAAGTAAA | 11783 |
rs51044431 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91037152 | CGAAGGACCACTGAA[A/G]CTCAAGGGTTCTAGA | 11783 |
rs51052418 | snp | G/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91033236 | GAAACAAACCAAATG[G/T]CAGAGCTTTGGTCCT | 11783 |
rs51090808 | snp | G/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91043419 | GATTCATCTTCTGCT[G/T]CATCCAAGAAACACA | 11783 |
rs51139673 | snp | G/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91061915 | CGCCTTCTAGTTTAA[G/T]AACTTCCCCATAGTG | 11783 |
rs51248816 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91029925 | TTTCTAAGGAGGCTT[C/T]TGAAGTAAGAGACTG | 11783 |
rs51255691 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91061607 | CACAAAGCAGGTTCC[A/G]GTGTTGATGTGCTAA | 11783 |
rs51288664 | snp | G/T | | | upstream-variant-2KB, intron-variant | Apaf1, Ikbip | GRCm38.p3 | 10:91084373 | TTTTTTTTTTTTTTT[G/T]GGGGGGGGGGTCTAT | 11783 |
rs51292745 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91029603 | GAATTGTTTGGGCCC[A/G]GCAGTAGTAGCGCAT | 11783 |
rs51341352 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91030232 | CTTTAACACACTTAA[A/G]ACAAACGGACATATT | 11783 |
rs51343933 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91062098 | AAAAAGACAGAAACT[C/T]CTTACCCATTACTGA | 11783 |
rs51376292 | snp | A/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91034204 | TCACAAACTCCCACC[A/T]GCTGTACTGAAACCT | 11783 |
rs51474280 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91043097 | CTATTTACTTAACCA[C/T]GCTGTTTTTAGGAAG | 11783 |
rs51530849 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91043811 | AAGAATATACCTTCT[C/T]CTCTGCACCTCAGGG | 11783 |
rs51548559 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91043194 | TAGCAAGGTAACTTA[A/G]ACTTAGATAAGTAAT | 11783 |
rs51581948 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91037426 | GCTCACAACTGCCTG[C/T]AACCTGAGCTCCAGA | 11783 |
rs51594992 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91043670 | AAACACAAGGGTATC[C/T]AAGTTCATAAAAAAA | 11783 |
rs51615636 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91028779 | CCACTGTGGGAAAGT[C/T]GCCGCTCCTCAAAAC | 11783 |
rs51621290 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91046236 | AATAGAGGACAAATA[C/T]TCAAAATACATAAAG | 11783 |
rs51670279 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:90999273 | CCAGCCTGTAAAAGG[C/T]TCATGTGGTGGCCTG | 11783 |
rs51671257 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91044089 | TTCTGGGAGGCAAGC[C/T]CATGACACTACATGC | 11783 |
rs51743739 | snp | A/C | | | intron-variant | Apaf1 | Mm_Celera | 10:91039580 | CCAGCACTTGGGAGG[A/C]AGAGGTAGGTGGATC | 11783 |
rs51804886 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91032713 | AGAGGAAGCATGGCT[C/T]CCGCTGTGCTGGGTA | 11783 |
rs51828491 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91038793 | TTCTAGAACACCAGA[A/G]AATTTAATCTACCTA | 11783 |
rs51834232 | snp | A/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91048609 | TGTGGTTGCTGGGAA[A/T]TGAACTCTGAACCTC | 11783 |
rs51853206 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91040157 | CACACACCTTTAATC[C/T]CAGCACTCTGGAAGC | 11783 |
rs51875816 | snp | A/C | | | intron-variant | Apaf1 | Mm_Celera | 10:91028689 | TTTAAATAGAAAAAT[A/C]GCGGTCAATGCTACC | 11783 |
rs51914155 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91038570 | TTGAGCCACAGTTTT[A/G]CTCTGTAGCCCTTGC | 11783 |
rs51958653 | snp | C/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91000378 | GAAGGTGACCACACT[C/G]AATAGAAAACAGGCA | 11783 |
rs51964839 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91048216 | GCTTTGAACACCTGC[A/G]TAACAACAGCACAGT | 11783 |
rs51995881 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91034514 | CTGTTTGATACTGAC[A/G]GAGTCAGAAGGAGGA | 11783 |
rs52019276 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91080645 | CTTCTCAACATGGAC[A/G]TCAGCCGCAGATCTT | 11783 |
rs52035030 | snp | A/C/G | | | intron-variant | Apaf1 | GRCm38.p3 | 10:91044078 | AATGAAAGCAGTTCT[A/C/G]GGAGGCAAGCTCATG | 11783 |
rs52036366 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91031868 | AAATCCAGCTTCCTG[C/T]AAGAACTAGACCTAG | 11783 |
rs52036542 | snp | G/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91043803 | AAACACAAAAGAATA[G/T]ACCTTCTCCTCTGCA | 11783 |
rs52037416 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91040071 | TAACGTGAACCCACT[C/T]CCTAGTCTCTAAATA | 11783 |
rs52052351 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91052395 | CTGGGAAAGGGGGAA[C/T]AGGAAGTATGAATTA | 11783 |
rs52053097 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91080613 | ACCTATAAACCAAGT[A/G]GCGTTGCTGATACCA | 11783 |
rs52120951 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91042172 | TAAATAAATAAATAA[A/G]CAAACATACATATAT | 11783 |
rs52174407 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91052809 | ACACACACATAAACA[C/T]ACATAAACACACATA | 11783 |
rs52209745 | snp | A/G | | | intron-variant | Apaf1 | GRCm38.p3 | 10:91040891 | TTAATATACACTAAT[A/G]ATTTTTTAAATAGAT | 11783 |
rs52226259 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91042872 | TTTTTTGCCTTTCCC[C/T]GCTTAGAGAAGAATT | 11783 |
rs52226377 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91039730 | CAGAAGAAAATCAAC[A/G]AAGATATTCTGCTAT | 11783 |
rs52343121 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91032234 | AAGAAAGGAAGGAGA[A/G]AGGAAGAAAGGGAGG | 11783 |
rs52375108 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91078719 | Cgggggggaggggag[A/G]gggtataggggactt | 11783 |
rs52383535 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91009931 | GGTGTAGGGGGGAGG[A/G]GTGGTTGGTTTGGTT | 11783 |
rs52385464 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91000669 | ATACATACATACATA[C/T]ACACACACATACATA | 11783 |
rs52534412 | snp | G/T | | | intron-variant | Apaf1 | GRCm38.p3 | 10:91070081 | TGTGTGTGTGTGTGT[G/T]TGTGTGTGTGTGTGT | 11783 |
rs52536034 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91042873 | TTTTTGCCTTTCCCT[A/G]CTTAGAGAAGAATTT | 11783 |
rs52536255 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91057105 | ACTAGTGGTAGTGAC[C/T]ATATATATATAGTCA | 11783 |
rs107600560 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91081028 | AGTAATATACAGAGC[A/G]CCGAAGAAGGGCAAG | 11783 |
rs107795529 | snp | A/G/T | | | intron-variant | Apaf1 | GRCm38.p3 | 10:91009909 | ATGGGTGTGGGGATG[A/G/T]GGGGGGGGTGTAGGG | 11783 |
rs107806173 | snp | G/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91065073 | CCCCCGGGATTCCAT[G/T]TGTGCATCATATACA | 11783 |
rs107961798 | snp | C/T | | | intron-variant, upstream-variant-2KB | Apaf1, Ikbip | Mm_Celera | 10:91081285 | CAGAGACAGGTGGAT[C/T]TCTGAGTTCGAGGCC | 11783 |
rs108021449 | snp | A/G | | | intron-variant, upstream-variant-2KB | Apaf1, Ikbip | Mm_Celera | 10:91081041 | GCGCCGAAGAAGGGC[A/G]AGAATCATTCAACTT | 11783 |
rs108121301 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91045841 | CCACCTACATATGGA[C/T]ACCTGGTCTTAGATA | 11783 |
rs108159245 | snp | G/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91065117 | CTTATTCCAAAACAC[G/T]GAACTTGAAGCTCAG | 11783 |
rs108356526 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91045714 | CTACTGGAGGTATCA[C/T]CCTCCCTGATTTCCA | 11783 |
rs108433892 | snp | A/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91065050 | AACTCCCATTCCCGC[A/T]TCCTCTGCCCCCGGG | 11783 |
rs108455170 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91043647 | TCAACTCTTAACATC[C/T]ATGCCCCAAACACAA | 11783 |
rs108532064 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:90991812 | AAATTTTTTTAATTA[A/G]GTATTTTCTTCATTT | 11783 |
rs108536823 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91045665 | AAAAAACAAAAAACC[C/T]AGGATAGCTAAACAA | 11783 |
rs108652048 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91045871 | AAAGAAGCCAAAATG[A/G]TACACTAGGGGGAAA | 11783 |
rs108758324 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91043683 | TCTAAGTTCATAAAA[A/G]AAATACTACTATGGC | 11783 |
rs108766568 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91065020 | AGTCTCACTCTATGG[C/T]CCAGGCTATCCTCAA | 11783 |
rs108839831 | snp | C/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91065048 | CAAACTCCCATTCCC[C/G]CATCCTCTGCCCCCG | 11783 |
rs108852416 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91065319 | CTGGGAATTGAACCC[A/G]GGTCATCTGGAAGGG | 11783 |
rs211702422 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91079672 | ATGTAAGAACGAACA[A/G]GCGAATATGTCTGCA | 11783 |
rs211769092 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:90992926 | TTCATATTTGTCTGT[A/G]CCCTTTGCAGTAGAA | 11783 |
rs211783934 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91078644 | ATCTGATCCCTTTTG[C/T]TGTACTGTGGATGTA | 11783 |
rs211787252 | in-del | -/A | | | intron-variant | Apaf1 | GRCm38.p3 | 10:91009909 | ATGGGTGTGGGGATG[-/A]GGGGGGGGTGTAGGG | 11783 |
rs211889981 | snp | C/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91044861 | ATCCCAGAGATGCAG[C/G]GATGATTCAATATAC | 11783 |
rs211897369 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91008925 | CTTAACTCAGGAAAC[C/T]TCAGTGGGCTGCCTA | 11783 |
rs211903454 | snp | C/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91017251 | GTTCTCCTCCCAGAG[C/G]CAGTTGGTACTAGTC | 11783 |
rs211923650 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91059485 | GGATTAAAGGCGTGC[A/G]CCACCACGCCCAGCC | 11783 |
rs211939382 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91016745 | AAACTCTCCTCTAAA[C/T]TCTTGAAGACTAGGA | 11783 |
rs211961821 | snp | G/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91065722 | TCCTGTGACTTCCAG[G/T]GCTAGCCAGGTAGGC | 11783 |
rs211971895 | snp | G/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91073833 | CTAAAAAATGAAGGA[G/T]CTGGTGAGACATACA | 11783 |
rs212034367 | snp | A/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91023197 | CAGCCGAGCATGGCT[A/T]TGTGTGCCTATTATT | 11783 |
rs212063475 | snp | A/C/T | | | intron-variant | Apaf1 | GRCm38.p3 | 10:91073232 | TTGTTTGTTTGCTTG[A/C/T]TTGATTGATTGTTTT | 11783 |
rs212082370 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91015503 | CCGTGGGTTAGCTGA[A/G]CCATAAAAACGTGTC | 11783 |
rs212101842 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91064472 | CAGGGTCTCTCTATG[C/T]ACCCTTGGCTGTCCT | 11783 |
rs212146825 | in-del | -/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91036349 | CCAGGCTGCGGCACA[-/G]GCACACGAGGTTTTA | 11783 |
rs212158458 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91021555 | AAATCCGCTTACATA[C/T]GCAACAAGATGCTGC | 11783 |
rs212178098 | snp | A/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91071504 | GGGTGTTTCTGAGAC[A/T]GCATCTCACCCTGCA | 11783 |
rs212234740 | in-del | -/GTGAGATGC | | | intron-variant | Apaf1 | Mm_Celera | 10:91009670 | GTAGTCACGGGCCTG[-/GTGAGATGC]GTCAGTGGGTAAGTG | 11783 |
rs212242017 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91032715 | AGGAAGCATGGCTTC[C/T]GCTGTGCTGGGTAGG | 11783 |
rs212249750 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91020909 | AAATTTAAAACTGGA[C/T]TGCACATAAATGATT | 11783 |
rs212251249 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91031309 | TGCTGTTTCCTACTG[C/T]GTGTCCTGGGAGAGT | 11783 |
rs212257940 | snp | A/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91070830 | ACACACACTAATAAA[A/T]AATTTGATTTTTTAA | 11783 |
rs212259864 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91077875 | ACGTTACCCTTCCAC[C/T]GTCTCAGAACACAAA | 11783 |
rs212267310 | in-del | -/A | | | intron-variant | Apaf1 | Mm_Celera | 10:91007156 | TTATGATAGAGATAG[-/A]AAAAAATCAATAAGA | 11783 |
rs212293267 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:90998622 | AAGCACTTCAAAGGT[A/G]TCCACTTATACCGAG | 11783 |
rs212346036 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91049723 | TACAAATGTCACTGA[A/G]TTAAGAGAAATCTAC | 11783 |
rs212376448 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91006484 | CTTCATCCCGACCCT[A/G]CACCTTCTCAAAGAC | 11783 |
rs212381126 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:90997712 | ACTTGTAAAATGGAC[A/G]ATGATTCCCATGGTG | 11783 |
rs212405711 | snp | A/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91057030 | TCTAGGACAGCCAGG[A/T]CTATACAGAGAAACC | 11783 |
rs212444888 | in-del | -/AATAATAATAATAATAAT | | | intron-variant | Apaf1 | GRCm38.p3 | 10:91079140 | TCTTGAAAAAAAACA[-/AATAATAATAATAATAAT]AATAATAATAATAAT | 11783 |
rs212481174 | in-del | -/A | | | intron-variant | Apaf1 | Mm_Celera | 10:91078422 | AATATATAAAATCTT[-/A]AAAAAAAAAAAAAAA | 11783 |
rs212481240 | in-del | -/AAG | | | intron-variant | Apaf1 | Mm_Celera | 10:91021468 | AAGGAAAAAGAAAAA[-/AAG]AGAGAGAGACAAGGA | 11783 |
rs212511776 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:90996547 | ATGCTGACTAATGAG[C/T]AGAGTACTAAAAAGA | 11783 |
rs212532684 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91056196 | TAACTCAAAATAAAT[A/G]TAAATGGGGCCACAA | 11783 |
rs212540427 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91004375 | TGACCCCAAAAACTC[C/T]ACTAGAGAACTCCTA | 11783 |
rs212561183 | in-del | -/CT | | | intron-variant | Apaf1 | Mm_Celera | 10:91043882 | AAATGACTCCCTACA[-/CT]CTATTAGACCATTAT | 11783 |
rs212578975 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91013453 | TGAAAAGGACCCCAT[A/G]GTAAACGTGGCTAAT | 11783 |
rs212608420 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91062643 | TCAGTGCCACGCCTG[C/T]TTGCTTTCTGCCAGG | 11783 |
rs212620950 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91055318 | TGGCAAAGAATGTAG[C/T]TGTTTCTGTGGCCAT | 11783 |
rs212624300 | in-del | -/A | | | intron-variant | Apaf1 | Mm_Celera | 10:91028533 | GCCTGGGCCTAGCAC[-/A]GGGTTCAACTCCCAG | 11783 |
rs212637486 | in-del | -/A | | | intron-variant | Apaf1 | Mm_Celera | 10:91023637 | ATTTTCCAAGAAAGC[-/A]TTCTCAGCAGTTAAG | 11783 |
rs212684582 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91058169 | GCATACAAATACACG[C/T]AGCCACAACATTCAT | 11783 |
rs212686538 | in-del | -/C | | | intron-variant | Apaf1 | Mm_Celera | 10:90997163 | TGTGGGGAAGAATGT[-/C]CCCCCCAAGCTAAAG | 11783 |
rs212695732 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91016113 | AACATCATGGAGAGG[A/G]CACTACAAAAGTGTA | 11783 |
rs212699375 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91077276 | CCACTAAGCCGTCTC[A/G]CCAGCCCGACGGATC | 11783 |
rs212726141 | in-del | -/ATGGATT | | | intron-variant | Apaf1 | Mm_Celera | 10:90993344 | AGGGTTTTCAGGGTA[-/ATGGATT]ACTCAATATCATTCT | 11783 |
rs212732744 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91064938 | AAGTTGTCAACTGGG[C/T]ACCAAGCTCCCTTAC | 11783 |
rs212793028 | snp | A/G | | | utr-variant-3-prime | Apaf1 | Mm_Celera | 10:90989892 | CCTATACAAGATTTT[A/G]TTCACTCTATTTACA | 11783 |
rs212794187 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91004988 | AGGGGGAAGGGGGAC[A/G]GGAAAGGGGGATTTC | 11783 |
rs212880481 | snp | A/C | | | intron-variant | Apaf1 | Mm_Celera | 10:90997008 | ATCTCCAGTGTTAAG[A/C]TGCTGTAATCCCAGC | 11783 |
rs212880803 | snp | C/T | | | downstream-variant-500B | Apaf1 | Mm_Celera | 10:90989024 | TCCAACAAAATTCCT[C/T]GTGGTTTTTTTTATT | 11783 |
rs212897337 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91048548 | AGCAGCTGCCTTCAG[A/G]CACACACCAGAAGAG | 11783 |
rs212921198 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91075484 | GATGGGGGAGGGCCA[A/G]CCTGGGTAGCATAGT | 11783 |
rs212923803 | snp | G/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91042315 | ATGATGATCCTATAA[G/T]AATTCCTAAAATTAT | 11783 |
rs212951064 | in-del | -/GCAA | | | intron-variant | Apaf1 | Mm_Celera | 10:90992550 | CAGACTCTTCAAAGT[-/GCAA]ACAAAGACAACGGTC | 11783 |
rs212993540 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91029397 | CAGAATGAGCTCCAG[A/G]ACAGACAGGGCTACA | 11783 |
rs212995580 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:90995882 | CATCATCTGTGATAT[A/G]TCTGGAAATCTTTCC | 11783 |
rs213025238 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91047665 | ACCAGAGCAGGAGGA[A/G]AAGGGAGTAGGAAAG | 11783 |
rs213028356 | in-del | -/AAAAAAAAA | | | intron-variant | Apaf1 | Mm_Celera | 10:91035698 | AGGCATACGTAAACC[-/AAAAAAAAA]AAAAAAACGATTCAT | 11783 |
rs213036393 | snp | A/C | | | intron-variant | Apaf1 | Mm_Celera | 10:90995535 | GTGGGGGTAACAACA[A/C]CGCCTCTTCTACTCT | 11783 |
rs213055156 | in-del | -/TCCCCCC | | | intron-variant | Apaf1 | GRCm38.p3 | 10:91032070 | CTGCTGGAACTAGGT[-/TCCCCCC]CCCCCCCGCCCATGT | 11783 |
rs213065614 | in-del | -/TTTATTTATTTA | | | intron-variant | Apaf1 | Mm_Celera | 10:91064623 | TCAGTTTTGTCTTTT[-/TTTATTTATTTA]TTTATTTATTTATTT | 11783 |
rs213101386 | in-del | -/CCT | | | intron-variant | Apaf1 | GRCm38.p3 | 10:90997972 | TCTCTCCTCATCCCC[-/CCT]CCCCCGCCCCAATAT | 11783 |
rs213107855 | snp | G/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91069771 | GCAGATTTAAATTTA[G/T]AGATGATGAGATGCC | 11783 |
rs213118295 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91020227 | TACAAACATATACAT[A/G]TATCTTAGCCACATC | 11783 |
rs213164228 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91019260 | TCCTATAGTACGAAA[C/T]GGTTGCTATTACATG | 11783 |
rs213199619 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91076798 | CAGGGCTACACAGGG[A/G]AACCTTGTCTCAGGG | 11783 |
rs213238017 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91029602 | AGAATTGTTTGGGCC[C/T]GGCAGTAGTAGCGCA | 11783 |
rs213257718 | in-del | -/AA | | | intron-variant | Apaf1 | Mm_Celera | 10:91063291 | AAATAAATGAAAAAT[-/AA]AAAAAACACAGAAGG | 11783 |
rs213266416 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91035980 | GGAGAAGACTCCAAA[A/G]GTGACAGATAAAACA | 11783 |
rs213278694 | snp | C/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91076210 | GTGCTGGAGAACTCG[C/G]CTCTCTCCAGTGACA | 11783 |
rs213337823 | in-del | -/AATA | | | intron-variant | Apaf1 | GRCm38.p3 | 10:91062996 | GAGAAACCCTGTCTC[-/AATA]AATAAATAAATAAAT | 11783 |
rs213362737 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91017359 | TGTTGGTCCTCCCCA[A/G]CTCTCCATGTGTGTC | 11783 |
rs213372003 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91074243 | TGCCATTTCATTCGG[A/G]AAACCCACCTCTTCC | 11783 |
rs213374197 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91035244 | AACCCTAAGAGTGGG[C/T]TGGGTTGTTTTATAC | 11783 |
rs213395032 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91066582 | AAAGAATCAACTCCT[A/G]AAAGTTGTCTTCTAA | 11783 |
rs213395145 | in-del | -/TACAGTACAG | | | intron-variant | Apaf1 | Mm_Celera | 10:91046164 | ACAAAGCAGCAGCTT[-/TACAGTACAG]TACAGTACAGTACAG | 11783 |
rs213437399 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91027678 | AAGCTAACACGCAGA[A/G]CAGCTCTCCCTGATG | 11783 |
rs213470567 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91033512 | TGCTTTAACTAACAA[C/T]CTTTAAAGAAAACGC | 11783 |
rs213488345 | snp | G/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91001643 | CAGTAGGCACTGTAA[G/T]TCACATGTGGCTCGG | 11783 |
rs213511564 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91073926 | AGAGACAAATCTCAC[C/T]AACCGTCCTCCGGCC | 11783 |
rs213524189 | snp | G/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91052764 | GTGTGTTGCTGCATA[G/T]CCACCCACACCCAAC | 11783 |
rs213542125 | in-del | -/CTAT | | | intron-variant | Apaf1 | Mm_Celera | 10:91033691 | GACCTTGACAAGCTG[-/CTAT]CTAACATCATTTTGC | 11783 |
rs213556917 | in-del | -/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91073737 | GCCACCATGATCACT[-/G]GTTAAGACTTGTACT | 11783 |
rs213560298 | snp | G/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91011784 | TGTGAGGAAGTGAAG[G/T]GTGTAAAAAAAGAGG | 11783 |
rs213589761 | snp | A/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91062463 | ATGCATTTACATGCT[A/T]TGTCCCCAGTTGATG | 11783 |
rs213593591 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91052011 | TGTCCTGTTATGTTA[C/T]AAGCACGCTATGAAT | 11783 |
rs213603782 | snp | A/C | | | intron-variant | Apaf1 | Mm_Celera | 10:91046851 | CACACACACACACTC[A/C]CTTCACACTTCCCCA | 11783 |
rs213628826 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91068912 | AATGTCTATTATTAT[C/T]ATTACTGTTAGAATT | 11783 |
rs213663475 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91011227 | TCTGGAGCCCGAAAC[A/G]GGGTCTGCCCCAGAA | 11783 |
rs213695827 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91061519 | ATGGTGGGTACATGC[A/G]ACGGTGTTTGAAGAA | 11783 |
rs213697600 | in-del | -/TA | | | intron-variant | Apaf1 | Mm_Celera | 10:91061124 | TCTTTCAACCTGTAG[-/TA]GATGGTCACGTTTTC | 11783 |
rs213707344 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91018492 | AGGAATGATTCAGCA[C/T]GCACAGTCCGGCTCC | 11783 |
rs213707843 | snp | A/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91050485 | ATCTGATGCTGCTTG[A/T]ATTCTAATGCTAAAT | 11783 |
rs213710257 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91059820 | AATACACTATTTCCT[C/T]GATATCTCTGGCTTA | 11783 |
rs213732445 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91008719 | AGAAAGCCTGGTCTG[C/T]ACAAAGCAAGTTCTA | 11783 |
rs213737594 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91067893 | ACCCGTAATGAGATC[C/T]GATACCCTCTTTTGG | 11783 |
rs213781796 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91017932 | CTATGATCGGGTTTC[C/T]GTCCTCCCCAGGCCT | 11783 |
rs213811666 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91008030 | GGGACAGTCTGGCTA[C/T]ATAGGAAGAGCCTAT | 11783 |
rs213824659 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91009349 | ACATGTAGATGCCTC[A/G]CATACACCTGGCCCC | 11783 |
rs213825338 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91058603 | CCCTTTAATCAAATA[A/G]TCAACATCTACATTA | 11783 |
rs213846346 | in-del | -/A | | | intron-variant | Apaf1 | Mm_Celera | 10:91072714 | TATAAAGTGGAGAGC[-/A]ATTGAAGATGATACC | 11783 |
rs213869969 | in-del | -/AGCCC | | | intron-variant | Apaf1 | Mm_Celera | 10:91051164 | AGGACCCAGTGTTTA[-/AGCCC]AGCCTGGACATCTAG | 11783 |
rs213879954 | in-del | -/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91035907 | GGCAAGGAAAAAAAA[-/T]AAAAATCCAAAAACA | 11783 |
rs214034144 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91051204 | GTCTTTAAAACAAGA[C/T]AAATAAAACCCATCT | 11783 |
rs214046066 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91078052 | GCCTGAGTTTGCTTA[A/G]CATGTGCAAGGTCAT | 11783 |
rs214065891 | snp | C/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91016283 | ATTAATGAGTGAGGG[C/G]CTTAGGAGGTACCAC | 11783 |
rs214108997 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91038475 | AGGTTTGAAGCTGGA[A/G]CATTTGCGTGCCAGG | 11783 |
rs214149324 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91010632 | AAAATTCTCTTTTTT[C/T]CACAGTATGGTTTTG | 11783 |
rs214168321 | snp | C/G | | | intron-variant | Apaf1 | Mm_Celera | 10:90997676 | CTCCAACAGCTCGGT[C/G]TCTCTAGCTTCAGTT | 11783 |
rs214184650 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91060871 | AGAGGCTGAACACAC[A/G]GGAGAGCTTCTGCAG | 11783 |
rs214217470 | snp | G/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91039548 | AAATAGACACCCAGG[G/T]GCACCTGACTTTAAC | 11783 |
rs214231462 | in-del | -/A | | | intron-variant | Apaf1 | Mm_Celera | 10:91048780 | TTACCCAACATGCAC[-/A]AGATCCTGAGTTCAC | 11783 |
rs214244899 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:90993056 | AGCCCGAGGAGACTC[A/G]CTCACTTTCAGAGAC | 11783 |
rs214296406 | in-del | -/TCAC | | | intron-variant | Apaf1 | Mm_Celera | 10:91046830 | ACATTCTCTCTTCTT[-/TCAC]TCACTCACACACACA | 11783 |
rs214366776 | snp | A/C | | | intron-variant | Apaf1 | Mm_Celera | 10:91031996 | CCCTGCCATTGGATC[A/C]CCTTCCCCTACCTGA | 11783 |
rs214399321 | snp | G/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91078460 | AAGAAAGAGACTTTA[G/T]AAGACTGGGAAGGAT | 11783 |
rs214399779 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91016700 | AAATTAAAATTTCTG[C/T]ACGTACTCTATTGGA | 11783 |
rs214403717 | snp | A/G | | | intron-variant | Apaf1 | GRCm38.p3 | 10:91031414 | TAAGAATTGTGAGCA[A/G]TTAGGAAGCCTGCGC | 11783 |
rs214420948 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91065645 | CTTTTGCATCCCTAA[A/G]TTGGTATTTCTGCCT | 11783 |
rs214443857 | snp | A/G | | | utr-variant-3-prime | Apaf1 | Mm_Celera | 10:90991155 | ATTTGAATGCATCAA[A/G]GAATTTACCAATAGC | 11783 |
rs214445214 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91023144 | GCATTTCTCATAAGC[A/G]TAAGGACCCGGGTTC | 11783 |
rs214495711 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91030903 | ACAGACACAATACAT[A/G]CACATAATTCAAACC | 11783 |
rs214531178 | snp | A/C | | | intron-variant | Apaf1 | Mm_Celera | 10:91037314 | AAATCAAACTGCCGA[A/C]GGGTCTATTTTAAGG | 11783 |
rs214548649 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91040141 | CAGGTATTATAGTGC[A/G]CACACACCTTTAATC | 11783 |
rs214577260 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:90993769 | TCCACAGCTAAATCC[A/G]CCTTTGCCTTCAGGT | 11783 |
rs214617493 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91036754 | CAGATTAAAACCTCC[A/G]AGACTGTAAACAAAT | 11783 |
rs214632968 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91006357 | GATGTAGTTAAGTTT[C/T]CTCCGTTTCAAAGAC | 11783 |
rs214633214 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91022172 | TCCCAGCAACCACAT[C/T]GTGGCTCACAACCAT | 11783 |
rs214656877 | snp | G/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91056875 | AATCAAAGTGCAAGG[G/T]TTACCACTCTTCTGT | 11783 |
rs214661838 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91072272 | AGAGGCATCATGGCA[C/T]ACACACACTACTGTA | 11783 |
rs214670247 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91005268 | CTAATACAAGTACTT[C/T]ATTTACCTCAAGGGA | 11783 |
rs214744413 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91056282 | AAATATAAAAGATTA[A/G]GAAAGGAAATCTTTG | 11783 |
rs214746372 | in-del | -/A | | | intron-variant | Apaf1 | Mm_Celera | 10:91056254 | TTAAATATGAAACAG[-/A]AAATTTTTTTAGAAA | 11783 |
rs214747864 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91064266 | TTCCATGGATGCTCT[A/G]CCAGTGAGCGGTGTG | 11783 |
rs214780539 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91044678 | ATTCATGTCATGAGG[C/T]CACAGTTACTCAGAC | 11783 |
rs214788229 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91063642 | TTCCACAGAGGTCCC[C/T]GAATCCTGAGGGGAA | 11783 |
rs214846937 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91070720 | GTGTGATCCCTGAAA[C/T]CCACAGAAGGGTGGA | 11783 |
rs214847601 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91002683 | GTGAGCATCTGTTGG[C/T]ATCCATAATAGTGTC | 11783 |
rs214882233 | snp | A/C/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91077254 | TCAGAGCAGTCAGTG[A/C/G]TCTCACCCACTAAGC | 11783 |
rs214887418 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91011761 | GCATCTTTATAGTAT[A/G]GGAGAACTGTGAGGA | 11783 |
rs214936744 | snp | A/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91062376 | CAAAGGCGAGATTAT[A/T]GTTTCAAGAGAAAAA | 11783 |
rs214970397 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91011377 | TGAAGATTCTAGAAA[C/T]CTAACCTGTATGTTG | 11783 |
rs214980859 | in-del | -/CC | | | intron-variant | Apaf1 | Mm_Celera | 10:91076471 | GATGTAATCACAGGG[-/CC]CTTATAAAGAGGAAA | 11783 |
rs214991581 | snp | G/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91073072 | TTATCCTAAAATATC[G/T]TTAGTATTCAATTCT | 11783 |
rs215023422 | snp | G/T | | | upstream-variant-2KB, intron-variant | Apaf1, Ikbip | Mm_Celera | 10:91084362 | TGAGTTTTTTGTTTT[G/T]TTTTTTTTTTGGGGG | 11783 |
rs215151041 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91003962 | ATATAGAAATCTATC[A/G]GTGTAATCCATGACA | 11783 |
rs215159023 | snp | G/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91055209 | AGGCCATCCTAGAAG[G/T]ACCTTGGAAGACCCA | 11783 |
rs215182799 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91014576 | AATCTTCAAAGGGGC[C/T]GTGAAACAGGCCTGA | 11783 |
rs215213151 | in-del | -/G | | | intron-variant | Apaf1 | GRCm38.p3 | 10:91032179 | ACTTGTAAAGTGGGA[-/G]GGGGGAGCTATGATC | 11783 |
rs215219702 | snp | A/G | | | intron-variant, upstream-variant-2KB | Apaf1, Ikbip | Mm_Celera | 10:91081275 | ACTCCGGAGGCAGAG[A/G]CAGGTGGATCTCTGA | 11783 |
rs215222246 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91020853 | GAGATTCTAGAAAGA[A/G]CAGTAAGGACCCAGT | 11783 |
rs215238798 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91041088 | CATGTTAGCACACGA[C/T]TAATCCCAGCACTTG | 11783 |
rs215261228 | snp | G/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91020368 | AGGAGCTCTGAGAAC[G/T]ATCATGTAATTAAAT | 11783 |
rs215280304 | snp | A/G | | | intron-variant | Apaf1 | GRCm38.p3 | 10:91070139 | AATCCCAGCACTTGG[A/G]AGGCAGAGGCAAGTG | 11783 |
rs215396063 | snp | C/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91076860 | ATGCAACTCAGTGGT[C/G]GAGCATCTGTTCGCA | 11783 |
rs215408725 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91019205 | GATTCACAGTTAAAA[C/T]GCATAGGATATAAAA | 11783 |
rs215424937 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91068849 | TAGTTTTACACTTCT[A/G]AAAGTTCCTTATAAA | 11783 |
rs215431428 | in-del | -/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91014346 | AGCTGTATTTAGCAC[-/T]TTTACGCTTTCGTTT | 11783 |
rs215450620 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91029517 | AAGGAAGGAGGGAGG[A/G]AAGATGCATGCAGTG | 11783 |
rs215472461 | in-del | -/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91060289 | ACAAGAGGAGAACCT[-/G]GGGGGGGGAGGTGGG | 11783 |
rs215496735 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91035017 | ATAAAGGAAATTGTG[A/G]CGGGGTAACAGGAAA | 11783 |
rs215503950 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91015462 | GGTAAAAGAAGAACT[C/T]GCAAGAGAGGAGAAA | 11783 |
rs215505963 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91042908 | CCTTTCCCCACTTAC[A/G]ACCTCTCCCCATTTC | 11783 |
rs215568168 | snp | A/G | | | intron-variant, upstream-variant-2KB | Apaf1, Ikbip | Mm_Celera | 10:91081996 | ATAAAGGCTAAGTCT[A/G]TCCAGGAAAACAGTA | 11783 |
rs215570523 | in-del | -/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91076538 | GCGGTGGTGAATGCC[-/T]TTAATTACAGCATTC | 11783 |
rs215632363 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:90996365 | GATGCTCTTCCAGAA[A/G]ACCCAGGTTCAATTC | 11783 |
rs215665485 | snp | A/G | | | synonymous-codon | Apaf1 | Mm_Celera | 10:91048158 | GCAGCAAAGCACCTC[A/G]TCTTCGTGAGCTTTG | 11783 |
rs215750701 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91039481 | CTCAGGGACAGAGCA[C/T]TTACTTAGCACATGG | 11783 |
rs215765549 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91010572 | GGATTGATTTGCATT[C/T]ATCTGCATGCTGACC | 11783 |
rs215798333 | snp | A/C | | | intron-variant | Apaf1 | Mm_Celera | 10:91060634 | AAACGATTTTCAATG[A/C]AAGTTACCCAAGACC | 11783 |
rs215801724 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91009589 | ATCAGTGGGCACAGG[A/G]ATACAGAAGGCTGGA | 11783 |
rs215834511 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91059979 | TACCCTCACCTCTCA[C/T]GTCAGTCCAACTACC | 11783 |
rs215835633 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91067066 | TGTACACTAACTCCA[C/T]CTGACCATCTGTACC | 11783 |
rs215881913 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91017269 | GTTGGTACTAGTCTG[A/G]AGAGCCTGGGCTCCC | 11783 |
rs215904404 | snp | G/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91053225 | AGAGCCCGTCTAAAT[G/T]GTAGGTGGGCCTGGC | 11783 |
rs215916001 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91066405 | AAGAGACCCTGCATC[A/G]TGGTACTAAGCCGGA | 11783 |
rs215938789 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91018731 | AAAGGATGTAATTAC[A/G]CACAGCCTCGAGGGA | 11783 |
rs215960919 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91029515 | GGAAGGAAGGAGGGA[A/G]GGAAGATGCATGCAG | 11783 |
rs215974138 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91007935 | GGTGTGGGATACATG[C/T]CTGTAATCCCAGCAT | 11783 |
rs216009013 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91016192 | ATGACAGGATTGTTA[C/T]ATGCATGAAATTACA | 11783 |
rs216055809 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91076127 | TTTCCCTGCAGCATC[A/G]TCTGCCAGAATAAAA | 11783 |
rs216090172 | snp | A/C | | | intron-variant | Apaf1 | Mm_Celera | 10:91072211 | GCTCAGTGAGTAAGG[A/C]CCAAGCTGACAACCT | 11783 |
rs216091139 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91015608 | AGATTCTACCAGCTT[A/G]GAGGGTAGGTAGCTG | 11783 |
rs216091625 | snp | C/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91064560 | GCTTCCCAAGTCCTG[C/G]GATTAAAGGCGTGCA | 11783 |
rs216092895 | snp | A/C | | | intron-variant | Apaf1 | Mm_Celera | 10:91042624 | TGGCTTTAACCCTTC[A/C]GTGAGCCAGTGAAGC | 11783 |
rs216103180 | in-del | -/ATAT | | | intron-variant | Apaf1 | GRCm38.p3 | 10:91000666 | TACATACATACATAC[-/ATAT]ACACACACATACATA | 11783 |
rs216130615 | in-del | -/A | | | intron-variant | Apaf1 | Mm_Celera | 10:91013737 | CAGTGGACACGGGGG[-/A]CCCTGTAGTAACATT | 11783 |
rs216131499 | in-del | -/GGTG | | | intron-variant | Apaf1 | Mm_Celera | 10:91035052 | GGAAGAAGAAAGGTA[-/GGTG]GGTGGGCTCCTAAAA | 11783 |
rs216167698 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91045594 | CAGATTCAATGCAAT[C/T]CCCATCAAAATTTCA | 11783 |
rs216201735 | in-del | -/TTTGT | | | intron-variant | Apaf1 | Mm_Celera | 10:91055107 | GGGGGAGGGGTGTTG[-/TTTGT]TTTGTTTTGTTGTTG | 11783 |
rs216244152 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91044892 | GAAATCAGTAAGTGT[A/G]ACCCACCATATAAAC | 11783 |
rs216260828 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91008682 | TCACATGGCTGAGAC[A/G]GGAAGATGGCCGAAA | 11783 |
rs216294032 | snp | G/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91059109 | GATGGGATCCTGAAT[G/T]GGATCTGGACCGTTG | 11783 |
rs216321844 | snp | A/G | | | utr-variant-3-prime | Apaf1 | Mm_Celera | 10:90989968 | AAGGAAGGGCTGGTC[A/G]TGTAGCCCAGCGGTG | 11783 |
rs216322771 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91023324 | AAGGCATCGGCATGT[A/G]CTTGCATGGATGTGC | 11783 |
rs216337468 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91073322 | CCTGAAACTCACTCT[A/G]TAGACCAGGCTGGCC | 11783 |
rs216386121 | snp | G/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91051960 | TGTTTGAAAAGGATT[G/T]CATTTAGTCACTAGC | 11783 |
rs216412630 | snp | A/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91046441 | TGACACCTGTCGGAA[A/T]GGCCAAGATCAATAA | 11783 |
rs216444175 | snp | G/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91079685 | CAGGCGAATATGTCT[G/T]CAGCACAAATTAGCT | 11783 |
rs216499765 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91000063 | TGAGAGGGAACTAAA[A/G]CAGCTCAGCGGTCGA | 11783 |
rs216508758 | snp | A/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91068287 | ATCACTATGGTTCTC[A/T]GAGAGCTCTGTTTGA | 11783 |
rs216523996 | snp | A/C | | | intron-variant | Apaf1 | Mm_Celera | 10:91071709 | GAATTTTAAAAAACT[A/C]AAAGTATCTTAATGG | 11783 |
rs216525544 | in-del | -/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91065387 | TTTTATTTTTAATCA[-/T]TTTTGCTGACTTCAG | 11783 |
rs216536334 | in-del | -/TT | | | intron-variant | Apaf1 | Mm_Celera | 10:91017160 | TGTCTTCAACACAGA[-/TT]TTTTTGCCTTAACCT | 11783 |
rs216537991 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91028871 | ATTAAAAGTTGGGCC[C/T]CCAGCAGATACATGT | 11783 |
rs216545459 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91017863 | AGATTATGTTTTTGA[C/T]CTAAGTATTAATGGA | 11783 |
rs216546194 | in-del | -/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91078705 | AAACATTTTTACGGC[-/G]GGGGGGAGGGGAGGG | 11783 |
rs216562270 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91075395 | CACAAGCTAAAGTCA[C/T]TTGAGAAGAGGGAAC | 11783 |
rs216606050 | in-del | -/ACT | | | intron-variant | Apaf1 | Mm_Celera | 10:91066997 | ACTTTAGAGAGAACA[-/ACT]GGAAAGAAGTGGCTC | 11783 |
rs216620264 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91038228 | AATAAAGCTATGGGT[C/T]TGAGACCACATATGG | 11783 |
rs216666243 | snp | A/G | | | utr-variant-3-prime | Apaf1 | Mm_Celera | 10:90991029 | ACCATACCCCCTGGG[A/G]GTAAGTGTGGTTCAG | 11783 |
rs216698310 | snp | C/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91044019 | AAAGACTTTTTAGAT[C/G]TAAATGAAAATGAAT | 11783 |
rs216698513 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91037567 | ATCTAAGTTAAATGG[A/G]AAAAGTAAAACTCAC | 11783 |
rs216715900 | snp | A/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91073884 | TAGCCTGAGTTTGGA[A/T]CCCCAGAACCTACAC | 11783 |
rs216774411 | snp | C/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91058449 | GTGCAGATCCTGAAA[C/G]CCACATCAAGCACAT | 11783 |
rs216783925 | snp | G/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91042863 | TTACTAGAATTTTTT[G/T]CCTTTCCCTGCTTAG | 11783 |
rs216852989 | in-del | -/C | | | intron-variant | Apaf1 | Mm_Celera | 10:91005486 | GTATGACAGCACACA[-/C]CTACAATTCTACCCA | 11783 |
rs216866211 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91042583 | ACTGAGTTTATCTAC[A/G]TAAAACTTCACTAGT | 11783 |
rs216894916 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91014316 | GAGACAACAAAGCCG[A/G]ACCCTAATCTCGGCA | 11783 |
rs216914840 | snp | C/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91063508 | AGCACTGAAGAAACT[C/G]ATCCTCTCGCTCCCA | 11783 |
rs216929806 | snp | A/G | | | synonymous-codon | Apaf1 | Mm_Celera | 10:91020719 | AGAAAACATCACACC[A/G]TGAACCCAACTCAAA | 11783 |
rs216938331 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91013512 | AAAGGTGAGAAGGAC[A/G]AGTGCTCCCTAAGTT | 11783 |
rs216942495 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91062732 | AGAGCTGCTTAGCCA[C/T]GGTGTCTCTTCACAG | 11783 |
rs216945645 | snp | A/C | | | intron-variant | Apaf1 | Mm_Celera | 10:91070634 | GAACAACACCCAATG[A/C]AGCTCATTATGTGAG | 11783 |
rs216977430 | in-del | -/A | | | intron-variant | Apaf1 | Mm_Celera | 10:91044718 | CAGAATGACCCCACC[-/A]AAAAAAATTACAGGT | 11783 |
rs216986172 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91021626 | CTGAAATCCCTCTGA[A/G]AACAACTTATTATAA | 11783 |
rs217014593 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91020282 | CCCAGTCTAAAACCT[C/T]TCATGGCAGAAAGGC | 11783 |
rs217018370 | snp | A/T | | | intron-variant | Apaf1 | GRCm38.p3 | 10:91069962 | TATCATAAATGAAAT[A/T]ATTTTCTCAATTTCT | 11783 |
rs217026476 | in-del | -/TTGT | | | intron-variant | Apaf1 | Mm_Celera | 10:91073212 | CTACCATTGCCTTTA[-/TTGT]TTGTTTGTTTGTTTG | 11783 |
rs217064389 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91011299 | GTAGTCCGCCCTCTC[A/G]CCTGCGCGGAGGAGG | 11783 |
rs217097208 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91018648 | GCCCACGCAGCGACA[C/T]ATCCAAGTCACTTCA | 11783 |
rs217125845 | snp | A/G/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91068036 | CCAAGGCTGAAGAGC[A/G/T]GGCTAGCTGTTCTTA | 11783 |
rs217157946 | snp | G/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91018015 | GCCACACTGATTGCG[G/T]TGACATATTGTCTCT | 11783 |
rs217182573 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91027621 | TTCTCTCAAGCTGGC[C/T]TAGGGAAGCAAAACC | 11783 |
rs217217086 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91047698 | AGATAGCATGGAATA[A/G]CTATGCACACCAAGG | 11783 |
rs217217796 | snp | A/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91075182 | GACTAAAGAGAACCA[A/T]TGTCGGCCTCTAGCT | 11783 |
rs217220175 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91067328 | CCTGAATAAACGCCA[A/G]TCTTCTGTCTCCTAT | 11783 |
rs217228860 | snp | A/C | | | intron-variant | Apaf1 | Mm_Celera | 10:91046507 | TAAGAAAAATGAACA[A/C]TAATTCACTGCTGGT | 11783 |
rs217256571 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:90998847 | TATTATTCATTTAAA[C/T]AGCAAGTGAGTGCTA | 11783 |
rs217278521 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91047423 | TTTTTACTTTCTTGG[A/G]GTCCCAAAGTTAGCT | 11783 |
rs217285575 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91011613 | CACAGCATCCAGTAC[C/T]CATCTTGTATGTCTG | 11783 |
rs217309605 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91049839 | ACCATGTCATGCAGT[A/G]GCCACAAAGGTCAGA | 11783 |
rs217338850 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:90993830 | CAGGCTAAGTGATAA[C/T]GTGTTTTCATTTATA | 11783 |
rs217378181 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91022137 | GCACTGGATGCTCTT[C/T]CGTAGGTCATGAGTT | 11783 |
rs217413278 | snp | A/C | | | intron-variant | Apaf1 | Mm_Celera | 10:91031953 | ATGTGGGTCCCCTAA[A/C]CAGCAGATCAGGGCC | 11783 |
rs217431693 | in-del | -/A | | | intron-variant | Apaf1 | GRCm38.p3 | 10:90997856 | CTATCTTTTGGGGGG[-/A]AGGGGGGATAGGGGA | 11783 |
rs217445178 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:90992964 | AGACACATATAACAC[C/T]GAGTTTGGTAAAGCT | 11783 |
rs217536575 | snp | C/G | | | intron-variant | Apaf1 | Mm_Celera | 10:90999125 | GCAGGGACAATGACA[C/G]CTATGATGTGATCAA | 11783 |
rs217583695 | in-del | -/G | | | intron-variant | Apaf1 | Mm_Celera | 10:90995522 | TCACCACTGCCAAGT[-/G]GGGGTAACAACACCG | 11783 |
rs217592351 | snp | A/C | | | intron-variant | Apaf1 | Mm_Celera | 10:90997027 | TGTAATCCCAGCTAA[A/C]ACAGGAAGGCTAAAA | 11783 |
rs217602947 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:90994522 | CAACATTAAGAGACT[C/T]TTATTTCCAATGCAG | 11783 |
rs217642365 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91072365 | ACTTTCAAAAGAAAA[C/T]TAGTCTACTTAAAAA | 11783 |
rs217646339 | snp | G/T | | | intron-variant | Apaf1 | Mm_Celera | 10:90997628 | ACAGCTTAGGGGTGA[G/T]GGAGACGGTCCACCC | 11783 |
rs217646371 | in-del | -/C | | | utr-variant-3-prime | Apaf1 | Mm_Celera | 10:90989681 | TGTTCACTTCACTAG[-/C]CCAGCTACAGAACAG | 11783 |
rs217649781 | snp | G/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91074377 | GTAATAGAATCTGAT[G/T]CCCTCTTCTGGTGTG | 11783 |
rs217653454 | snp | A/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91005136 | GTGGGAGAGGTGAGG[A/T]GAAAGGATCACAAGT | 11783 |
rs217660689 | in-del | -/AAA | | | intron-variant | Apaf1 | Mm_Celera | 10:91001380 | TAAACCACAAGATAG[-/AAA]AAAAAAAAAAAAAAC | 11783 |
rs217686404 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91056230 | CTTAACTCACAGTTA[C/T]ATAAAGAATTTAAAT | 11783 |
rs217718783 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91071885 | CCATGACAGCACAGC[A/G]TTTAGTTAAACAGTG | 11783 |
rs217725617 | in-del | -/AC | | | intron-variant | Apaf1 | Mm_Celera | 10:91036725 | CTTGCCTTGGCACAG[-/AC]ACAGAGACAGGGTCA | 11783 |
rs217729674 | in-del | -/G | | | intron-variant | Apaf1 | GRCm38.p3 | 10:91078437 | AAAAAAAAAAAAAAA[-/G]AGAAAGAAAGAAAGA | 11783 |
rs217742735 | snp | A/C | | | intron-variant | Apaf1 | Mm_Celera | 10:91041047 | TGCTCTACACCTCTG[A/C]TGAGAAAGCTTACAG | 11783 |
rs217774173 | in-del | -/AAAAAAAA | | | intron-variant | Apaf1 | Mm_Celera | 10:91065922 | CTGTCTCGAAAAACC[-/AAAAAAAA]AAAAAAAAATACAGT | 11783 |
rs217878019 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91021831 | GTACACCGTGCTCTT[C/T]CCACCCACGCTTACG | 11783 |
rs217879225 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91031344 | ACTATTTCTGACTTG[C/T]ATGACTATGACCTTT | 11783 |
rs217897884 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91078354 | AACCATCTGTAATGA[A/G]ATCCAATGCCCTCTT | 11783 |
rs218020046 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91048415 | CAGAGAAGTATCCAT[C/T]GTTAAGGCTTGCAAA | 11783 |
rs218023062 | in-del | -/A | | | intron-variant | Apaf1 | Mm_Celera | 10:91005763 | TTTGGCAACACACAT[-/A]AAAAAAATTGGAACC | 11783 |
rs218029159 | snp | A/C | | | intron-variant | Apaf1 | Mm_Celera | 10:91049964 | TCTCAGACACTGAGC[A/C]ATCTCTCTAGCCCCT | 11783 |
rs218052769 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91076835 | TGTGCAACAGGAACA[A/G]GATGTAAAAATGCAA | 11783 |
rs218054186 | in-del | -/AA | | | intron-variant | Apaf1 | Mm_Celera | 10:91034908 | GCTTTCTTTATAAGT[-/AA]AAAAAAAACCCACAC | 11783 |
rs218061021 | in-del | -/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91066799 | ATCTAGTTGCTTAGA[-/T]TTTTTTCCCCTTGTT | 11783 |
rs218075292 | in-del | -/TTTT | | | intron-variant | Apaf1 | Mm_Celera | 10:90991787 | CCACCCCAGAAGTTC[-/TTTT]TTTTTTTAAAAATTT | 11783 |
rs218130014 | snp | A/C | | | intron-variant | Apaf1 | Mm_Celera | 10:91016385 | CCACTGACTGACTGC[A/C]ATACCCCAGTAACTA | 11783 |
rs218136688 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91020443 | GGTGCTGTGCAAGCA[A/G]CTTACTCACCGGACT | 11783 |
rs218156799 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91022304 | AAAGTAGGAAACACT[A/G]CAGTAAAGGACAGAA | 11783 |
rs218157508 | snp | G/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91036680 | AATAGGTAAGCAGTT[G/T]CTTTCACCACACGCT | 11783 |
rs218157673 | snp | C/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91015800 | GGTCCATAAAGGGAA[C/G]TCATACGTAGTGGTC | 11783 |
rs218171487 | snp | A/C | | | intron-variant | Apaf1 | Mm_Celera | 10:91077769 | GTGAACAAAACTTGA[A/C]AGTGACTACTTTTCG | 11783 |
rs218191536 | snp | G/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91044106 | ATGACACTACATGCC[G/T]AGATAGAAAAACTGG | 11783 |
rs218191882 | snp | A/C | | | intron-variant | Apaf1 | Mm_Celera | 10:90996814 | GCTTTGAATTCAGAG[A/C]TGCACCTGCCTCTGC | 11783 |
rs218197973 | in-del | -/CAAT | | | intron-variant | Apaf1 | Mm_Celera | 10:91034181 | GGCAAGCTAGGGCAG[-/CAAT]CGATCAATCACAAAC | 11783 |
rs218233661 | in-del | -/GAAAG | | | intron-variant | Apaf1 | Mm_Celera | 10:91020252 | ACATCATGAAGTAAA[-/GAAAG]GAAAGGAGATGTGTC | 11783 |
rs218237955 | in-del | -/AAAC | | | intron-variant | Apaf1 | Mm_Celera | 10:91062083 | AACCAAGTTAAAAAA[-/AAAC]AAAAGACAGAAACTC | 11783 |
rs218249490 | snp | A/C | | | intron-variant | Apaf1 | Mm_Celera | 10:91076254 | CACTGCCGGGAGACA[A/C]GCACGCTACACTGTG | 11783 |
rs218268417 | in-del | -/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91005617 | CTTTAAAAAAATAAA[-/T]CAAATAAATAAATAA | 11783 |
rs218291087 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91048686 | CCTATATTGACAAAT[C/T]CTAAACAACCAAATA | 11783 |
rs218411526 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91004585 | TCTGTACGACTCTTC[C/T]AGTCTTAACAGCCTG | 11783 |
rs218415104 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:90996016 | AGGAGGCAGAGGCAG[A/G]AAGATTTTGAGTTCA | 11783 |
rs218435806 | snp | A/G | | | utr-variant-3-prime | Apaf1 | Mm_Celera | 10:90990538 | GGTAAAAGGGGAAGT[A/G]TGTGTTACCGCTTCA | 11783 |
rs218438824 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91055360 | CTGCCTAAGGCTAAA[C/T]TGAAGAGTTTAGATT | 11783 |
rs218471289 | snp | A/T | | | intron-variant | Apaf1 | Mm_Celera | 10:90997354 | TGGAAGGCAATTAGG[A/T]TTGTTTAGGAATGTC | 11783 |
rs218563314 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91019799 | CTGCATGTAACTCTA[A/G]AATATATAAATAAGT | 11783 |
rs218580500 | snp | C/G | | | upstream-variant-2KB | Apaf1, Ikbip | Mm_Celera | 10:91082880 | GGGGCTAAGCCGCGG[C/G]CTCGCGCCCAGCTAG | 11783 |
rs218639404 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91047819 | GTCCTTTAACCCCGC[C/T]CACTCCTGCCTGTTA | 11783 |
rs218641705 | in-del | -/TC | | | intron-variant | Apaf1 | Mm_Celera | 10:91008764 | CACAGCAAGGCCTTG[-/TC]TCTCACAAAAGAAGA | 11783 |
rs218670266 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91047550 | AGAGCACACAGCATG[C/T]ACCTGGGCCATTAGG | 11783 |
rs218670391 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91054043 | AGACCCTCCTCCTAG[C/T]TGCCTGGAAACCAGT | 11783 |
rs218678453 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91061649 | CATCAGCCTGCTTTA[C/T]ACCAGAGCGTCAGCA | 11783 |
rs218679690 | in-del | -/CCAGCTTGTAGGG | | | intron-variant | Apaf1 | Mm_Celera | 10:91064342 | GACTGCCTTAAGAAT[-/CCAGCTTGTAGGG]CCAGCCTGGTAGTGC | 11783 |
rs218708883 | snp | A/G | | | intron-variant | Apaf1 | GRCm38.p3 | 10:91070216 | TCAGCCAAGGCTACA[A/G]AGAGAAACCCTGTCT | 11783 |
rs218765812 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91074567 | TTGATCTCCCATGCC[C/T]AAAACTGTCACTTAC | 11783 |
rs218795490 | snp | A/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91076959 | GAGGACAGAAGCAAA[A/T]CAGTACCACTGAGAA | 11783 |
rs218801039 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91074065 | GGTTGTACATTTATT[A/G]CTGGTGAATATCATC | 11783 |
rs218801210 | snp | A/T | | | intron-variant, upstream-variant-2KB | Apaf1, Ikbip | Mm_Celera | 10:91081356 | TGCAGAGAAACCCCG[A/T]TATGAAAAGATTTTT | 11783 |
rs218827554 | snp | A/C | | | intron-variant | Apaf1 | Mm_Celera | 10:91076490 | TATAAAGAGGAAAAC[A/C]AGTCCAAGTCAGAAA | 11783 |
rs218841237 | snp | A/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91028327 | AAAAAGGAGCAAACA[A/T]GGGTGAAGCCTTGGG | 11783 |
rs218854990 | snp | A/C | | | intron-variant | Apaf1 | Mm_Celera | 10:91028781 | ACTGTGGGAAAGTTG[A/C]CGCTCCTCAAAACCA | 11783 |
rs218868501 | in-del | -/ATAC | | | intron-variant | Apaf1 | GRCm38.p3 | 10:91000668 | CATACATACATACAT[-/ATAC]ACACACATACATACA | 11783 |
rs218881898 | snp | A/C | | | intron-variant | Apaf1 | Mm_Celera | 10:91001962 | ACCAAGATACAAACG[A/C]CTGAAGAAAGAGTAT | 11783 |
rs218912884 | snp | A/G | | | synonymous-codon | Apaf1 | Mm_Celera | 10:91001055 | CAATCTTGAATCTTG[A/G]AGGAGCCTGAAGTCC | 11783 |
rs218920200 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91034729 | TAACCAGACTGTGGG[A/G]CATACTTTTTTCTTC | 11783 |
rs218941983 | snp | C/G/T | | | intron-variant | Apaf1 | GRCm38.p3 | 10:90995934 | TGCTGGATCAGAATG[C/G/T]TATCAGTTTCCAAAG | 11783 |
rs218942197 | in-del | -/AGAGACAGAGAC | | | intron-variant | Apaf1 | Mm_Celera | 10:91029025 | AGAGGGAGGGAGAGG[-/AGAGACAGAGAC]AGAGACAGAGACAGA | 11783 |
rs218989738 | in-del | -/CAAAA | | | intron-variant | Apaf1 | Mm_Celera | 10:91039676 | CCTTGTTCCCCCCAC[-/CAAAA]CAAAACAAAACAAAA | 11783 |
rs218992289 | snp | G/T | | | intron-variant | Apaf1 | Mm_Celera | 10:90995597 | GTAAGTGAAAACCAC[G/T]TAGCTATGACACCGA | 11783 |
rs219038056 | snp | A/C | | | intron-variant | Apaf1 | Mm_Celera | 10:91003791 | AAACCATACAAAGAC[A/C]CAACAAAGAAAGATA | 11783 |
rs219038369 | in-del | -/C | | | intron-variant | Apaf1 | Mm_Celera | 10:91022214 | ACAAATAAAAAAAAA[-/C]CCTTTGGGTCAGAGC | 11783 |
rs219056415 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91052813 | ACACATAAACACACA[C/T]AAACACACATAAACA | 11783 |
rs219066755 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91033914 | ACTAACTGGCCACAC[C/T]ACTGGCTAGTAAATA | 11783 |
rs219092715 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91060308 | GGGGGAGGTGGGGAG[A/G]TGATTACATTAATAC | 11783 |
rs219094842 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91050730 | AGCACTGCATGGCCA[A/G]GAGAAACAGCAAATA | 11783 |
rs219109065 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91053070 | TCTGACCTCTCCAGG[C/T]ACTTACATGCATGGA | 11783 |
rs219122752 | snp | A/G | | | synonymous-codon | Apaf1 | Mm_Celera | 10:91059681 | GAGAGACTTATTAAC[A/G]AACTCCTGCAGGATG | 11783 |
rs219131432 | snp | C/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91052376 | CGTTAAAAGATGGTT[C/G]AGTCTGGGAAAGGGG | 11783 |
rs219153775 | in-del | -/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91051742 | TACCCGAGAGGCAAG[-/T]GGAGGTAGGGTTTCC | 11783 |
rs219168624 | snp | A/C | | | intron-variant | Apaf1 | Mm_Celera | 10:91062346 | ATGTATGGCCATGAA[A/C]AAGAGTCAGGGTAGC | 11783 |
rs219207778 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91023430 | TTAAAGCAAAAAGAA[A/G]TGCCTCAGAAACCAA | 11783 |
rs219240430 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:90999959 | TGGTAGAATTCTTGT[C/T]TAGTGAGTGCAAAGC | 11783 |
rs219255961 | snp | A/C | | | intron-variant | Apaf1 | Mm_Celera | 10:90999458 | TCCTCTGACCTGTAC[A/C]CATGCACAGTGACTC | 11783 |
rs219256087 | in-del | -/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91080167 | GTAAGGAAAACAGGA[-/T]TTTTTTTATTATTAT | 11783 |
rs219265243 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91051905 | ACAAATGCAAACAAT[A/G]CACACCTTCAAACAT | 11783 |
rs219271007 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91051301 | GGTAACAAGTGGACG[C/T]GTGAACAAACTACTG | 11783 |
rs219280304 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91009392 | AATCAAGTATTCACT[A/G]GAAAGGCCAATGGCA | 11783 |
rs219310954 | in-del | -/G | | | intron-variant | Apaf1 | GRCm38.p3 | 10:91030797 | ACACCCCGATCAGGA[-/G]GATCCCGGTCACTGT | 11783 |
rs219312030 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91059867 | TCCAAGATAAAATGA[A/G]AAACCGGGTGCTTCT | 11783 |
rs219352000 | in-del | -/C | | | intron-variant | Apaf1 | Mm_Celera | 10:91021569 | CGCAACAAGATGCTG[-/C]CTCCGAGACAAAGCA | 11783 |
rs219362270 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91051473 | AACCATTCTGTGACC[A/G]AGTGTCACAGGCTGG | 11783 |
rs219368778 | in-del | -/TATAG | | | intron-variant | Apaf1 | GRCm38.p3 | 10:91032691 | AACTATACTGAAAGC[-/TATAG]TGAGAGGAAGCATGG | 11783 |
rs219416258 | snp | G/T | | | intron-variant | Apaf1 | Mm_Celera | 10:90994780 | ATAAAGCTTACAGGG[G/T]GCCCAAGTGGCCAGC | 11783 |
rs219448680 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:90998956 | ACAATGACACCTACA[C/T]ACTCCTCTATACTGC | 11783 |
rs219460191 | in-del | -/AA | | | intron-variant | Apaf1 | GRCm38.p3 | 10:91032491 | CCTTGCACAGGGTGG[-/AA]AAAGTGGCTAAAGAT | 11783 |
rs219466843 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91034381 | GAGATGTACACACTC[A/G]TACGCAAAAATAGGC | 11783 |
rs219495341 | snp | C/T | | | intron-variant, upstream-variant-2KB | Apaf1, Ikbip | Mm_Celera | 10:91081244 | GGGCATCGTGGCCCA[C/T]GCCTTTAATCCCAGC | 11783 |
rs219500761 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:90998220 | GGCAGAGCAGCTAAC[A/G]CTGCCTGAGTCAGGA | 11783 |
rs219520998 | in-del | -/ATCTAGC | | | intron-variant | Apaf1 | Mm_Celera | 10:91034776 | AAGGCCTAGTATAGT[-/ATCTAGC]ATCCAGTGAATACTA | 11783 |
rs219524068 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:90993393 | ACATGTTATCAAAGA[C/T]TTATCCAAAATCACG | 11783 |
rs219525497 | snp | G/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91000089 | GTCGAGAGCACTGGC[G/T]GCTTTCCCAGAGGAG | 11783 |
rs219591875 | in-del | -/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91008470 | TAAATAGCATATTAA[-/T]TTTACGTATGTGGAC | 11783 |
rs219617914 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91022565 | ATCAGACACATGACT[C/T]CCATCTTACCCTGTT | 11783 |
rs219691052 | snp | A/C | | | intron-variant | Apaf1 | Mm_Celera | 10:91049865 | TCAGAAAACGCCACG[A/C]TATCCCCTGGAACTG | 11783 |
rs219719805 | in-del | -/TGGCAGGACT | | | intron-variant | Apaf1 | GRCm38.p3 | 10:91031526 | TGGAGTGGGTTGAGA[-/TGGCAGGACT]TGGCAGGACTTACGA | 11783 |
rs219721303 | in-del | -/CC | | | intron-variant | Apaf1 | GRCm38.p3 | 10:90997968 | TTCTTCTCTCCTCAT[-/CC]CCCCTCCCCCGCCCC | 11783 |
rs219741466 | in-del | -/CAATGAAAC | | | intron-variant | Apaf1 | Mm_Celera | 10:91044231 | AACGGTGCAAACAAT[-/CAATGAAAC]CAATGAAACAAAGAG | 11783 |
rs219765273 | snp | A/C | | | intron-variant | Apaf1 | GRCm38.p3 | 10:91031507 | TTGAAACTTTGTGTC[A/C]GAGTGGAGTGGGTTG | 11783 |
rs219817404 | snp | G/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91040235 | GTGAGTCCCAGAGCA[G/T]CCAGGGCTACACACT | 11783 |
rs219825260 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91077738 | CTGTCCTTACTGAAA[C/T]CCAAACCAAGCAGGA | 11783 |
rs219843428 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91064760 | TTTGTTTTCTTCTAT[A/G]TCTGTTGCTAAAAGA | 11783 |
rs219856159 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91077103 | CCTCCAAAGGAATTC[A/G]GTTCTAATGCTTTGA | 11783 |
rs219874531 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91079023 | CCAGGCAGTGGTGGT[A/G]CACGCCTTTAATCCC | 11783 |
rs219882210 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91038532 | CACCGTATCCTTGTG[A/G]AAAGTTGTAAAACCG | 11783 |
rs219907774 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:90998983 | CTGCAGAGACAATGA[C/T]ACCTACATACTCTTC | 11783 |
rs219926439 | in-del | -/C | | | intron-variant | Apaf1 | Mm_Celera | 10:91037749 | CACTACACTTTTATT[-/C]TGGACACTAAACTAA | 11783 |
rs219926607 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91006729 | CAAGTTTGAAGTAAA[A/G]CCTGAGCCACATAAT | 11783 |
rs219946791 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91008175 | CACCACTGTGATGGC[A/G]GGTCTGATGAATGGC | 11783 |
rs219956919 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91005829 | CAGGCAAATCATGAA[A/G]TAGTCTTTTTGTTTT | 11783 |
rs219974695 | snp | A/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91058841 | AACATGGGTGCTCTC[A/T]GTGCCATCTCTCCAG | 11783 |
rs219988983 | snp | G/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91031118 | ACCTCACAAGCATCT[G/T]TATGTAGAGTTCCAG | 11783 |
rs219993121 | in-del | -/A | | | intron-variant | Apaf1 | GRCm38.p3 | 10:91034240 | GACCTGCAGGCTAAC[-/A]AAAGGAACAGCTGAG | 11783 |
rs220022250 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91030650 | TTACTTTAGGAAAAA[C/T]CTCACAGTTTCATTC | 11783 |
rs220025187 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91037708 | TTTAGATCAACATCT[C/T]AGTCCACCAAGGAAC | 11783 |
rs220086528 | snp | A/C | | | missense | Apaf1 | Mm_Celera | 10:91054410 | AGGCGCCCAGTATCC[A/C]CCTCCTGCTTGGCCT | 11783 |
rs220090307 | in-del | -/AAA | | | intron-variant | Apaf1 | Mm_Celera | 10:91009269 | AAAAAAAAAAAAAAA[-/AAA]CCACAAGAAATTAAT | 11783 |
rs220091793 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91062877 | CCAGGCAGTGGTGGC[A/G]CATGCCTTTAATCCC | 11783 |
rs220104754 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91065143 | CTCAGAAATCCTTCT[C/T]TCTGACATAGTCTCA | 11783 |
rs220112166 | snp | A/G | | | synonymous-codon | Apaf1 | Mm_Celera | 10:91036937 | GTCAGCTGAGCAGCT[A/G]GCCAAGAGCTCATCG | 11783 |
rs220129696 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91062558 | AAGTTTCAAAAGCCC[A/G]TGCCAGGGCAAGTGT | 11783 |
rs220158135 | snp | A/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91031157 | ACGCCTTCTTCTGGC[A/T]TCCACGGCATTACAT | 11783 |
rs220166185 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91057441 | AGAGGAAAAAAGGAT[C/T]CATTTTCTATGGTCA | 11783 |
rs220190570 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91056398 | ATGTGCAAACATACA[C/T]AAACATACAAATACA | 11783 |
rs220208222 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91014635 | AAATTGAAATGTATA[C/T]ACTCTGAATCACTCA | 11783 |
rs220225170 | snp | G/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91029626 | TAGCGCATGCCTTTA[G/T]TCCCAGCACTTGGGA | 11783 |
rs220241190 | snp | A/C | | | intron-variant | Apaf1 | Mm_Celera | 10:91063708 | GTCCAAGGTCTCTCT[A/C]TGCACGGTGTCTCTG | 11783 |
rs220315024 | in-del | -/AAC | | | intron-variant | Apaf1 | Mm_Celera | 10:91045116 | AAGCAATCCATCAGG[-/AAC]AAAACTCTCCAAATA | 11783 |
rs220364521 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91013178 | ATATACTACACAGCA[A/G]AACAAAAAATGGGGC | 11783 |
rs220369259 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91007238 | AGAAAGTTGAGATTC[C/T]TTATGGTACATTCCT | 11783 |
rs220373801 | snp | C/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91055512 | TCTCATTATCACCAG[C/G]CATGGTGGCTTAAAC | 11783 |
rs220375820 | in-del | -/GAAGTGCA | | | intron-variant | Apaf1 | Mm_Celera | 10:91037217 | TCAAGGTGGAAAGAG[-/GAAGTGCA]GACTGGGAATGGTGG | 11783 |
rs220397762 | snp | A/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91057806 | CCTTAGAACACATAC[A/T]GTGGAAGGAGGGAGC | 11783 |
rs220409021 | in-del | -/A | | | intron-variant | Apaf1 | Mm_Celera | 10:91035814 | GAAAAATCTGTGAAT[-/A]AAGTTTTAAAATACT | 11783 |
rs220430329 | in-del | -/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91016472 | GGTGGGCTATTTATT[-/G]GAAAAGGGGGGGCTC | 11783 |
rs220440775 | in-del | -/TTTTTTTTTTTT | | | intron-variant | Apaf1 | Mm_Celera | 10:90996715 | AATATCTACCTAACA[-/TTTTTTTTTTTT]TTTTTTTTTTTTTGG | 11783 |
rs220464862 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91001833 | TTGCCGGCTTTTAAA[C/T]CCTTAACTTCGATTA | 11783 |
rs220510544 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91004741 | AACATGCTGTGTTAA[C/T]TGAATCACGGTAGTA | 11783 |
rs220543643 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91055594 | AGGCCAGCCTGGTCT[A/G]CATAGTTAAGTTCCA | 11783 |
rs220548265 | snp | A/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91000987 | AACAAACCATTTTTT[A/T]AAAAATCTAGTATGT | 11783 |
rs220553978 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:90996746 | TTTTTTTTTGGAGAC[A/G]GGATCTTACTAGCCC | 11783 |
rs220580955 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91010848 | GTTTTTGTTATCCTG[A/G]GATATTTGTTATTCC | 11783 |
rs220606958 | in-del | -/AGAG | | | intron-variant | Apaf1 | Mm_Celera | 10:91034003 | AATGACAATGAATGC[-/AGAG]ACCCATGACTGACAA | 11783 |
rs220624814 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91036283 | TAAAAACGCTGCTCC[A/G]GCTTAGATCTAGGAA | 11783 |
rs220625401 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91013625 | TGCAATAGCTTTTCT[A/G]CATCAGTGTCTGATT | 11783 |
rs220630573 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91004661 | CCTCTACCACAGGAA[A/G]TCAGAGATCCTTCCT | 11783 |
rs220634765 | in-del | -/AGAG | | | intron-variant | Apaf1 | Mm_Celera | 10:91007149 | TAAGACTGTTATGAT[-/AGAG]ATAGAAAAAATCAAT | 11783 |
rs220657900 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91035661 | GCTACACAGGAGCAG[A/G]TACTGAAGACAGCTC | 11783 |
rs220676798 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91063187 | CTCTTCTAGCTTCCA[C/T]GGGCATTAAGCACAC | 11783 |
rs220695182 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91035490 | GCAGACGGCTCAGGG[A/G]CAGACCTGACTCCTG | 11783 |
rs220700980 | snp | C/G | | | intron-variant, upstream-variant-2KB | Apaf1, Ikbip | Mm_Celera | 10:91081235 | TTCTCAGCCGGGCAT[C/G]GTGGCCCACGCCTTT | 11783 |
rs220766953 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91041899 | GCTTCAGACTATTAT[A/G]TAATCTGCGACAGGG | 11783 |
rs220769703 | snp | C/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91041795 | ACAGATAACAAAGAT[C/G]TTCTCCTCCAACCTT | 11783 |
rs220863634 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91062577 | CAGGGCAAGTGTATG[A/G]TTCCCTGCCAGCTGC | 11783 |
rs220892782 | in-del | -/G | | | utr-variant-3-prime | Apaf1 | Mm_Celera | 10:90989579 | CTCCAGAGCTGCTGC[-/G]GTGTGAGCCACAGCC | 11783 |
rs220951482 | snp | A/G | | | upstream-variant-2KB, intron-variant | Apaf1, Ikbip | Mm_Celera | 10:91083560 | GGATGAGTTTGCTCC[A/G]CCCTCCACCAAAAAT | 11783 |
rs220971511 | snp | A/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91069323 | AAATAAATAAAGGAA[A/T]TTTAAAAACCTAGTT | 11783 |
rs220997002 | in-del | -/AC | | | intron-variant | Apaf1 | Mm_Celera | 10:91072840 | CACATGTTTGCACAT[-/AC]ACACACACACATGTA | 11783 |
rs221015503 | snp | A/C | | | upstream-variant-2KB, intron-variant | Apaf1, Ikbip | Mm_Celera | 10:91084418 | TTTGGTTTTTTGAGA[A/C]AGGCTCTTAGGTAGC | 11783 |
rs221022517 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91009988 | AAGAGACTTTTTACT[A/G]CATAGAGATGGAGGA | 11783 |
rs221037391 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91042681 | GATAATCACTCCTAA[C/T]GGATATGCATGTAGA | 11783 |
rs221042393 | in-del | -/ATAA | | | intron-variant | Apaf1 | Mm_Celera | 10:91073993 | CGCAGCTACACACAC[-/ATAA]AGATGAATATTGTTA | 11783 |
rs221055481 | in-del | -/AGCCTG | | | intron-variant | Apaf1 | Mm_Celera | 10:91017296 | TCCCTGTGCTACACC[-/AGCCTG]AGCATTGAAGCTTTG | 11783 |
rs221069843 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91033830 | CCACTGCTAGTGACA[C/T]TCACACACGAATACA | 11783 |
rs221124711 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91067659 | TCACCATGGTAGGCA[C/T]GGTGACTACCATGGT | 11783 |
rs221136292 | in-del | -/GTTTTTTTTTTTTTTTG | | | upstream-variant-2KB, intron-variant | Apaf1, Ikbip | GRCm38.p3 | 10:91084357 | GTCCTTGAGTTTTTT[-/GTTTTTTTTTTTTTTTG]GGGGGGGGGGTCTAT | 11783 |
rs221137669 | snp | A/C/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91040404 | TCAGACCTCTGCATG[A/C/G]TGTCAGTAGCAGAGG | 11783 |
rs221139274 | snp | A/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91033277 | ATCTATGAGAAATCA[A/T]ACAGTTAGTAGGACA | 11783 |
rs221172535 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91058908 | AGACAGCAGACAAAG[C/T]CAAGTTAGGGAACTG | 11783 |
rs221174476 | snp | C/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91065885 | GAGTGAGTTCCAGGA[C/T]AGTCAGAGCTACACA | 11783 |
rs221207748 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91065248 | GTATGTCTGTGTGAG[A/G]GTGTTGGATCCTCTG | 11783 |
rs221258265 | snp | G/T | | | intron-variant | Apaf1 | Mm_Celera | 10:91061092 | TTGGAAGCAGAGAGA[G/T]GTCGTCATGGGAGCT | 11783 |
rs221274997 | in-del | -/AGA | | | intron-variant | Apaf1 | Mm_Celera | 10:91032521 | TTGGTGTTGACAGTG[-/AGA]AGGAGTGTAAAAGGG | 11783 |
rs221302632 | snp | A/C | | | intron-variant | Apaf1 | Mm_Celera | 10:91067532 | CTAGTCTTTGTTCCC[A/C]GTGACCATTCTCAGA | 11783 |
rs221305066 | snp | A/G | | | intron-variant | Apaf1 | Mm_Celera | 10:91060485 | GTGGGTGGGTGGGGT[A/G]TGGGGGTATGAGTGT | 11783 |
rs221378081 | in-del | -/GTTGTTGTTG | | | upstream-variant-2KB, intron-variant | Apaf1, Ikbip | GRCm38.p3 | 10:91084361 | TGAGTTTTTTGTTTT[-/GTTGTTGTTG]TTTTTTTTTTTGGGG | 11783 |