SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs3089180 | snp | C/T | 0.15879 | 0.232768 | intron-variant | Hecw1 | Mm_Celera | 13:14323900 | GAACCTGGCAGAGGG[C/T]GTCAAGGGCTCCAGA | 94253 |
rs3089181 | snp | A/G | 0.15879 | 0.232768 | intron-variant | Hecw1 | Mm_Celera | 13:14323917 | TCAAGGGCTCCAGAG[A/G]ACTCTCCATGCAACA | 94253 |
rs3089182 | snp | C/T | 0.15879 | 0.232768 | intron-variant | Hecw1 | Mm_Celera | 13:14323936 | CTCCATGCAACAGGA[C/T]CCCTAGCACAGAAGA | 94253 |
rs3660499 | snp | C/G | 0.290657 | 0.246672 | utr-variant-3-prime | Hecw1 | Mm_Celera | 13:14230629 | CTGTTCAGGACAATG[C/G]CAGGCAAGGCTCCAC | 94253 |
rs3680731 | snp | G/T | 0.5 | 0 | intron-variant | Hecw1 | Mm_Celera | 13:14354063 | ACTATTAACATTAAA[G/T]TGTTGGTTATATCAA | 94253 |
rs3698795 | snp | C/T | 0.32 | 0.24 | intron-variant | Hecw1 | Mm_Celera | 13:14263967 | AATATTCCTGGCTAA[C/T]TATTCCAAATTCAGT | 94253 |
rs6160389 | snp | C/G | 0.5 | 0 | intron-variant | Hecw1 | Mm_Celera | 13:14294875 | ATTATGAGAATGACT[C/G]TCATAGACTCGTATT | 94253 |
rs6190978 | snp | A/C | 0.5 | 0 | intron-variant | Hecw1 | Mm_Celera | 13:14302469 | taggtgatttgagtc[A/C]attaatattgagaga | 94253 |
rs6191466 | snp | G/T | 0.5 | 0 | intron-variant | Hecw1 | Mm_Celera | 13:14302549 | ggctttatgcgcttt[G/T]ggttctttcTAGCAA | 94253 |
rs6191978 | snp | A/C | 0.5 | 0 | intron-variant | Hecw1 | Mm_Celera | 13:14302613 | tttttggtggaattg[A/C]aaactggtagaaaca | 94253 |
rs6226958 | snp | A/C | 0.456747 | 0.140554 | intron-variant | Hecw1 | Mm_Celera | 13:14265728 | TTTTTATGCCATGTA[A/C]CTCTTTGTATTAAAT | 94253 |
rs6227100 | snp | A/T | 0.5 | 0 | intron-variant | Hecw1 | Mm_Celera | 13:14265813 | TGCACATTATTCTTT[A/T]TTCTCCTCCAATTTT | 94253 |
rs6232794 | snp | C/T | 0.5 | 0 | intron-variant | Hecw1 | Mm_Celera | 13:14454368 | agagactctacctag[C/T]agtagactgaaacag | 94253 |
rs6233383 | snp | A/C | 0.5 | 0 | intron-variant | Hecw1 | Mm_Celera | 13:14454488 | gggaatcccatagga[A/C]ggccaacagagtcaa | 94253 |
rs6233470 | snp | C/G | 0.5 | 0 | intron-variant | Hecw1 | Mm_Celera | 13:14454540 | tctcagaatctgagt[C/G]accaaccaaagaaca | 94253 |
rs6271979 | snp | A/C | 0.5 | 0 | intron-variant | Hecw1 | Mm_Celera | 13:14352257 | TGCTACCACTAAAAT[A/C]CCAGTCAAAAGGTCC | 94253 |
rs6277406 | snp | G/T | 0.5 | 0 | intron-variant | Hecw1 | Mm_Celera | 13:14274747 | cttaatcagtaaaaa[G/T]aaaaacccaaatggc | 94253 |
rs6305058 | snp | A/C | 0.492188 | 0.0620098 | intron-variant | Hecw1 | Mm_Celera | 13:14431748 | ATGCCTTATAAATAT[A/C]TACTCTTCCTTTGGG | 94253 |
rs6305518 | snp | C/T | 0.5 | 0 | intron-variant | Hecw1 | Mm_Celera | 13:14431810 | TTACCTTAAAGGCTA[C/T]ATAAGAAANTTCATA | 94253 |
rs6305529 | snp | C/T | 0.5 | 0 | intron-variant | Hecw1 | Mm_Celera | 13:14431819 | AGGCTANATAAGAAA[C/T]TTCATATATCAATGT | 94253 |
rs6306004 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Hecw1 | Mm_Celera | 13:14431898 | CTATGACTTTAGATC[A/G]AAGTTTTCTGTTTTG | 94253 |
rs6306084 | snp | A/T | 0.456747 | 0.140554 | intron-variant | Hecw1 | Mm_Celera | 13:14431954 | AAGTACAAATTATGG[A/T]TTAAGGATTGTTTAA | 94253 |
rs6306574 | snp | G/T | 0.5 | 0 | intron-variant | Hecw1 | Mm_Celera | 13:14432021 | AAAAAAAATGAGGCC[G/T]CAGNCTTCATCAGGA | 94253 |
rs6306579 | snp | A/T | 0.456747 | 0.140554 | intron-variant | Hecw1 | Mm_Celera | 13:14432025 | AAAATGAGGCCNCAG[A/T]CTTCATCAGGACCAG | 94253 |
rs6306990 | snp | C/G | 0.456747 | 0.140554 | intron-variant | Hecw1 | Mm_Celera | 13:14432063 | TAGGACACCAGAGAT[C/G]ACTGGGCAATAAGCC | 94253 |
rs6311311 | snp | C/T | 0.5 | 0 | intron-variant | Hecw1 | Mm_Celera | 13:14354914 | ccatgatagctgcgt[C/T]actaaaatcccatga | 94253 |
rs6320267 | snp | C/T | 0.456747 | 0.140554 | intron-variant | Hecw1 | Mm_Celera | 13:14432316 | ATTGAAATTGTTAAA[C/T]TAACTCAGGTTCTTT | 94253 |
rs6320311 | snp | C/G | 0.391111 | 0.206368 | intron-variant | Hecw1 | Mm_Celera | 13:14432335 | CTCAGGTTCTTTTTA[C/G]TTCACAATAGAAGTT | 94253 |
rs6320777 | snp | C/T | 0.415225 | 0.187619 | intron-variant | Hecw1 | Mm_Celera | 13:14432394 | GCCAAGCATCCTAAT[C/T]CTGGGAGCAGCCCTC | 94253 |
rs6321362 | snp | C/T | 0.32 | 0.24 | intron-variant | Hecw1 | Mm_Celera | 13:14432477 | TTGAATACCGTCTAA[C/T]AGGGGAAANATGTCA | 94253 |
rs6321369 | snp | C/T | 0.5 | 0 | intron-variant | Hecw1 | Mm_Celera | 13:14432486 | GTCTAANAGGGGAAA[C/T]ATGTCAAAGATGCCA | 94253 |
rs6321991 | snp | A/G | 0.456747 | 0.140554 | intron-variant | Hecw1 | Mm_Celera | 13:14432621 | TTGTGTAATGGCGGA[A/G]ATTTAGTCAAAGTTA | 94253 |
rs6323002 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Hecw1 | Mm_Celera | 13:14432770 | TGGATGTTTAGTAGT[A/G]CAGAGTTAAATGCAA | 94253 |
rs6323555 | snp | A/T | 0.5 | 0 | intron-variant | Hecw1 | Mm_Celera | 13:14432864 | TCTAATGAAGAAGGC[A/T]GCCCTGTGTATGAGA | 94253 |
rs6324138 | snp | C/G | 0.207612 | 0.24638 | intron-variant | Hecw1 | Mm_Celera | 13:14432957 | ACAAACCAACACACA[C/G]TGAACATCAAGGNGC | 94253 |
rs6324156 | snp | A/G | 0.456747 | 0.140554 | intron-variant | Hecw1 | Mm_Celera | 13:14432970 | CANTGAACATCAAGG[A/G]GCTTTCTTATTCTTT | 94253 |
rs6325118 | snp | A/G | 0.5 | 0 | intron-variant | Hecw1 | Mm_Celera | 13:14355127 | attttacccagctat[A/G]caccctgaaagttat | 94253 |
rs6326936 | snp | C/G | 0.5 | 0 | intron-variant | Hecw1 | Mm_Celera | 13:14355494 | gtcatagcattctca[C/G]acttaaaagagagca | 94253 |
rs6391390 | snp | A/G | 0.5 | 0 | intron-variant | Hecw1 | Mm_Celera | 13:14442813 | GGATTTTTGAGGAAG[A/G]CAAGATCATTCATNG | 94253 |
rs6391424 | snp | A/G | 0.5 | 0 | intron-variant | Hecw1 | Mm_Celera | 13:14442827 | GNCAAGATCATTCAT[A/G]GGTAAAgactatata | 94253 |
rs6392507 | snp | A/G | 0.5 | 0 | intron-variant | Hecw1 | Mm_Celera | 13:14443007 | AATACAAAAGACTGA[A/G]CATGTAAATGTTTTA | 94253 |
rs6393133 | snp | C/T | 0.5 | 0 | intron-variant | Hecw1 | Mm_Celera | 13:14443121 | ATCCTTAAAGAAAGC[C/T]GCAGTTTCTAGTTTA | 94253 |
rs6393588 | snp | A/G | 0.5 | 0 | intron-variant | Hecw1 | Mm_Celera | 13:14443160 | TTCTTTTTCCTAAGG[A/G]AAAGAACAATTAGCA | 94253 |
rs6402137 | snp | C/T | 0.49827 | 0.0293608 | intron-variant | Hecw1 | Mm_Celera | 13:14320440 | tttGCTTTCCATCAC[C/T]CAGTAAGCAGTTTTT | 94253 |
rs6402218 | snp | A/T | 0.456747 | 0.140554 | intron-variant | Hecw1 | Mm_Celera | 13:14320485 | TAAAAAGTGCTGAAG[A/T]TGGCCTTTGTGTCCT | 94253 |
rs6402684 | snp | C/T | 0.456747 | 0.140554 | intron-variant | Hecw1 | Mm_Celera | 13:14320524 | AAGTCTGTATGTTCT[C/T]CCAGGACCTGCCTTT | 94253 |
rs6402827 | snp | C/G | 0.5 | 0 | intron-variant | Hecw1 | Mm_Celera | 13:14320606 | AGGTAGTCAGTGACA[C/G]TTCTAAAGGGAAGAT | 94253 |
rs6403350 | snp | G/T | 0.5 | 0 | intron-variant | Hecw1 | Mm_Celera | 13:14320675 | GTACTACAGTtgtgt[G/T]tgtgtgtgtgtgtgt | 94253 |
rs6403786 | snp | A/T | 0.456747 | 0.140554 | intron-variant | Hecw1 | Mm_Celera | 13:14320712 | gtATCCTGGGGGTGG[A/T]CCATGGCTCAAGGCA | 94253 |
rs6404521 | snp | A/C | 0.5 | 0 | intron-variant | Hecw1 | Mm_Celera | 13:14320909 | AAAACCAATAGGGTG[A/C]NTGTATATCTTATCA | 94253 |
rs6404522 | snp | A/G | 0.5 | 0 | intron-variant | Hecw1 | GRCm38.p3 | 13:14320909 | AAACCAATAGGGTGN[A/G]TGTATATCTTATCAG | 94253 |
rs6404950 | snp | A/G | 0.456747 | 0.140554 | intron-variant | Hecw1 | Mm_Celera | 13:14320951 | AAGTAATCCCACAAA[A/G]ACTTGTTGCTCCTAC | 94253 |
rs6412298 | snp | A/T | 0.5 | 0 | intron-variant | Hecw1 | Mm_Celera | 13:14437667 | aatgaggccttcacc[A/T]tacaaaaagaaggac | 94253 |
rs13481700 | snp | A/G | 0.432133 | 0.171253 | intron-variant | Hecw1 | Mm_Celera | 13:14309400 | AATTATTGAATACCA[A/G]ATTATGTTTTAACAA | 94253 |
rs13481701 | snp | A/G | 0.108728 | 0.206258 | intron-variant, upstream-variant-2KB | Hecw1, Gm30893 | Mm_Celera | 13:14521082 | TAGGCAACTGTCTTC[A/G]TGAAAATCTGTCCCC | 94253 |
rs29224060 | snp | C/T | 0.375 | 0.216506 | intron-variant | Hecw1 | Mm_Celera | 13:14337306 | ATCTTTAATTTCTTT[C/T]TTTATTTCCTCTTTG | 94253 |
rs29224342 | snp | C/T | 0.5 | 0 | intron-variant | Hecw1 | Mm_Celera | 13:14362836 | AGACTGAAGGAAAGA[C/T]CATCCAGAGACTGCC | 94253 |
rs29226154 | snp | A/G | 0.375 | 0.216506 | intron-variant | Hecw1 | Mm_Celera | 13:14363258 | TATAGGGGAATGATA[A/G]GGCAGAGAGGCAGGA | 94253 |
rs29226358 | snp | G/T | 0.32 | 0.24 | intron-variant | Hecw1 | Mm_Celera | 13:14296967 | ACAAAATCACTCCAT[G/T]GAAAATTTAAAGGTG | 94253 |
rs29227173 | snp | A/T | 0.375 | 0.216506 | intron-variant | Hecw1 | Mm_Celera | 13:14337285 | TTCTTATTAAATTTT[A/T]AAAAAATCTTTAATT | 94253 |
rs29228127 | snp | C/T | 0.375 | 0.216506 | intron-variant | Hecw1 | Mm_Celera | 13:14333405 | AGTACTACCTGAGGA[C/T]ACAGCTATATCACTC | 94253 |
rs29228151 | snp | A/T | 0.48 | 0.0979796 | intron-variant | Hecw1 | Mm_Celera | 13:14273103 | GTTTTCCCCACCCTA[A/T]CTATTCAAGGCCCTC | 94253 |
rs29228225 | snp | A/C | 0.475309 | 0.108333 | intron-variant | Hecw1 | Mm_Celera | 13:14352741 | AAACAATGGCATCTG[A/C]GATAAAGATAAGACT | 94253 |
rs29228283 | snp | G/T | 0.375 | 0.216506 | intron-variant | Hecw1 | Mm_Celera | 13:14307483 | CAGATCCCTTGGAAC[G/T]GGAGTTGCAGACAGT | 94253 |
rs29228350 | snp | A/C | 0.507812 | 0.180704 | intron-variant | Hecw1 | Mm_Celera | 13:14269588 | AGCATGTGTAATGTT[A/C]CATTCTTCTATATTG | 94253 |
rs29228685 | snp | A/T | 0.32 | 0.24 | intron-variant | Hecw1 | Mm_Celera | 13:14246711 | AATATATCTAAGAAA[A/T]TTTATACCAATTTAG | 94253 |
rs29229528 | snp | A/G | 0.375 | 0.216506 | intron-variant | Hecw1 | Mm_Celera | 13:14341183 | AAGTGTACAGCTGAA[A/G]ATATTATTGTCCAGT | 94253 |
rs29230855 | snp | C/T | 0.375 | 0.216506 | intron-variant | Hecw1 | Mm_Celera | 13:14255709 | TTCTTGTCATACAGA[C/T]CTTTCACTTGCTTGG | 94253 |
rs29234904 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Hecw1 | Mm_Celera | 13:14346601 | AGCAGATGCCCACTT[C/T]TTTTTTCTTTGTATA | 94253 |
rs29235768 | snp | A/G | 0.493827 | 0.0552116 | intron-variant | Hecw1 | Mm_Celera | 13:14356215 | TAAGAAAAATGAGAA[A/G]AATACAAAGATAAAT | 94253 |
rs29239717 | snp | C/T | 0.375 | 0.216506 | intron-variant | Hecw1 | Mm_Celera | 13:14324379 | ATTTTTTAAAAATTG[C/T]ATTCAACATTTTTGT | 94253 |
rs29242328 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Hecw1 | Mm_Celera | 13:14340390 | AGCACTGACCACAAC[C/T]ACAGTCATGCATTAT | 94253 |
rs29245332 | snp | A/G | 0.456747 | 0.140554 | intron-variant | Hecw1 | Mm_Celera | 13:14319779 | TTCAAAGTAACTTTT[A/G]AATTACTGAAAATTT | 94253 |
rs29245449 | snp | A/G | 0.375 | 0.216506 | intron-variant | Hecw1 | Mm_Celera | 13:14317934 | TGTTCAACTCTTAAC[A/G]TTTAACAGTGAACGC | 94253 |
rs29248827 | snp | G/T | 0.375 | 0.216506 | intron-variant | Hecw1 | Mm_Celera | 13:14315336 | TTTTGTGACCTGTGG[G/T]GGGATTAGTTAGTGG | 94253 |
rs29248944 | snp | A/G | 0.498615 | 0.0262793 | utr-variant-3-prime | Hecw1 | GRCm38.p3 | 13:14229338 | TGACCATTATGGTTA[A/G]ATTTATCTCAAATGT | 94253 |
rs29249205 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Hecw1 | Mm_Celera | 13:14361881 | GATCAACAATTGACA[A/T]ATGGGACCTAATAAA | 94253 |
rs29249359 | snp | C/T | 0.5 | 0 | intron-variant | Hecw1 | Mm_Celera | 13:14238044 | TTACAAGAGGCTTGG[C/T]ATTTGCTTGTTTTTT | 94253 |
rs29250411 | snp | C/T | 0.432133 | 0.171253 | intron-variant | Hecw1 | Mm_Celera | 13:14317965 | TGTTTAACTCTACCT[C/T]CCTTGGCTGGAAATA | 94253 |
rs29251965 | snp | G/T | 0.188366 | 0.242283 | intron-variant | Hecw1 | Mm_Celera | 13:14361650 | AAAGGTTGTATTCCA[G/T]TTCTTCCAGATAAAA | 94253 |
rs29300106 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Hecw1 | GRCm38.p3 | 13:14346624 | TATGGGAGGGGTCGA[A/G]GGAGAATTATACAAA | 94253 |
rs29494519 | snp | A/C/G | 0.444444 | 0.157135 | intron-variant | Hecw1 | GRCm38.p3 | 13:14236125 | AGAGGGAGGGAGGAA[A/C/G]AGAGAGAGAGAATAT | 94253 |
rs29494646 | snp | A/G | 0.456747 | 0.140554 | intron-variant | Hecw1 | Mm_Celera | 13:14252672 | CTATCCTTTGCTAAG[A/G]CTGGACACAGGAAAT | 94253 |
rs29495399 | snp | A/G | 0.33241 | 0.236027 | utr-variant-3-prime | Hecw1 | Mm_Celera | 13:14229279 | ACTTTCATTTATGTC[A/G]TATTTCAGACAACAT | 94253 |
rs29509191 | snp | C/T | 0.375 | 0.216506 | intron-variant | Hecw1 | Mm_Celera | 13:14348078 | ACACACACACACATA[C/T]ACATATACACATACA | 94253 |
rs29509571 | snp | C/T | 0.375 | 0.216506 | intron-variant | Hecw1 | Mm_Celera | 13:14333138 | ATAAAGAATTTTCAA[C/T]TGAGGAATATTGAAC | 94253 |
rs29510556 | snp | C/T | 0.487535 | 0.077957 | intron-variant | Hecw1 | Mm_Celera | 13:14234614 | TTTAGATAGGCAAGA[C/T]TTAACTAATTTATAT | 94253 |
rs29511024 | snp | C/T | 0.375 | 0.216506 | intron-variant | Hecw1 | Mm_Celera | 13:14335116 | TTCATTGATTCTTGA[C/T]CTTAGAGCATAAGCC | 94253 |
rs29514142 | snp | C/G | 0.5 | 0 | intron-variant | Hecw1 | Mm_Celera | 13:14238038 | TGATGCTTACAAGAG[C/G]CTTGGCATTTGCTTG | 94253 |
rs29514796 | snp | C/T | 0.387812 | 0.208586 | synonymous-codon | Hecw1 | Mm_Celera | 13:14265157 | CTTGTTTCTCTGGAG[C/T]TCCTTCCTTGAGTAT | 94253 |
rs29516288 | snp | A/C | 0.207612 | 0.24638 | intron-variant | Hecw1 | Mm_Celera | 13:14252506 | CAATGATTTGAGAAT[A/C]CAAATTATGATCTCT | 94253 |
rs29516598 | snp | C/T | 0.359862 | 0.224567 | intron-variant | Hecw1 | Mm_Celera | 13:14307367 | AACAGCTCTTGTGTT[C/T]AAACCCCTTTTAACT | 94253 |
rs29529802 | snp | A/G | 0.375 | 0.216506 | intron-variant | Hecw1 | Mm_Celera | 13:14345637 | TTTGGTGGTTTGAAT[A/G]AGAACTGTCCCACAT | 94253 |
rs29529978 | snp | A/G | 0.375 | 0.216506 | intron-variant | Hecw1 | Mm_Celera | 13:14255728 | TCACTTGCTTGGTTT[A/G]ATCACACCAAGGTAT | 94253 |
rs29547966 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Hecw1 | Mm_Celera | 13:14309873 | GGGAAGACTTTCAAA[A/C]CACATGTCAGAAATA | 94253 |
rs29548178 | snp | A/G | 0.498615 | 0.0262793 | intron-variant | Hecw1 | Mm_Celera | 13:14264416 | CAAATGAACTCCTAC[A/G]ACAATTGTATTTCAA | 94253 |
rs29548795 | snp | A/G | 0.188366 | 0.242283 | intron-variant | Hecw1 | Mm_Celera | 13:14361672 | CAGATAAAAAGACTG[A/G]CAAAGTAACACTGCA | 94253 |
rs29549947 | snp | A/G | 0.265928 | 0.249492 | intron-variant | Hecw1 | Mm_Celera | 13:14246894 | CTATTATGTAGTTTC[A/G]AAGATACAGAAATAC | 94253 |
rs29550999 | snp | A/G | 0.49827 | 0.0293608 | intron-variant | Hecw1 | Mm_Celera | 13:14312311 | TATGGATATGAGGGC[A/G]TCATAATTAAAACAA | 94253 |
rs29551488 | snp | C/T | 0.375 | 0.216506 | intron-variant | Hecw1 | Mm_Celera | 13:14348082 | ACACACACATACACA[C/T]ATACACATACACACA | 94253 |
rs29552402 | snp | C/T | 0.375 | 0.216506 | intron-variant | Hecw1 | Mm_Celera | 13:14255760 | TTATATTATTTGTGA[C/T]TATTGTGAAGGGTGT | 94253 |
rs29556455 | snp | A/G | 0.375 | 0.216506 | intron-variant | Hecw1 | Mm_Celera | 13:14232677 | GTAAGGAGGTGGATA[A/G]CCATATGACAAGAAG | 94253 |
rs29566975 | snp | C/T | 0.277778 | 0.248452 | synonymous-codon | Hecw1 | Mm_Celera | 13:14316105 | GGCAGCCAGTTCATC[C/T]TGCCAAGGGCCAGCC | 94253 |
rs29568023 | snp | A/G | 0.475309 | 0.108333 | intron-variant | Hecw1 | Mm_Celera | 13:14252688 | CTGGACACAGGAAAT[A/G]GAATACTCATGAGCT | 94253 |
rs29570368 | snp | C/T | 0.188366 | 0.242283 | intron-variant | Hecw1 | Mm_Celera | 13:14358600 | GGTCATTGCCATATT[C/T]TCCCATTGTCAGACA | 94253 |
rs29573408 | snp | A/G | 0.359862 | 0.224567 | intron-variant | Hecw1 | Mm_Celera | 13:14251397 | CTAACAATTGCAAGG[A/G]CTTTAAAACCACAGA | 94253 |
rs29580136 | snp | A/G | 0.33241 | 0.236027 | intron-variant | Hecw1 | Mm_Celera | 13:14233847 | ACTGTAGAGACCCAT[A/G]AATATACATGATCCC | 94253 |
rs29588667 | snp | G/T | 0.265928 | 0.249492 | intron-variant | Hecw1 | Mm_Celera | 13:14235123 | CAGGGTTTGAGTTTG[G/T]CATGGGACGAATTTA | 94253 |
rs29589133 | snp | C/T | 0.197531 | 0.244432 | intron-variant | Hecw1 | Mm_Celera | 13:14298923 | CCATTCTCTTTAAAC[C/T]TCCAAGACTCAATTC | 94253 |
rs29613736 | snp | A/G | 0.375 | 0.216506 | intron-variant | Hecw1 | Mm_Celera | 13:14370675 | GCTATTAATACAAAT[A/G]CTTTTTCTTTTGTTT | 94253 |
rs29625384 | snp | C/G | 0.5 | 0 | utr-variant-3-prime | Hecw1 | Mm_Celera | 13:14229378 | GCCAGGCTGTCTGTG[C/G]AGCCTGTGATTGTTT | 94253 |
rs29632259 | snp | A/G | 0.375 | 0.216506 | intron-variant | Hecw1 | Mm_Celera | 13:14275673 | ATGAGAATGTGATAC[A/G]TATACAACATAGAAT | 94253 |
rs29635140 | snp | A/G | 0.188366 | 0.242283 | intron-variant | Hecw1 | Mm_Celera | 13:14324344 | AGTCCTCTTTACTAG[A/G]TTCTATTTTCATATC | 94253 |
rs29670679 | snp | A/T | 0.5 | 0 | intron-variant | Hecw1 | Mm_Celera | 13:14346415 | ACCTAAGGCTGTAAA[A/T]TTTGAATGACAGTCC | 94253 |
rs29680329 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Hecw1 | Mm_Celera | 13:14327937 | TGGTCCAAGGATATA[C/G]AAACCATCACAGTTA | 94253 |
rs29680441 | snp | A/G | 0.465374 | 0.126941 | intron-variant | Hecw1 | Mm_Celera | 13:14246854 | TCTACGCATACTGGA[A/G]TACTAAGTGGATGTA | 94253 |
rs29681469 | snp | G/T | 0.391111 | 0.206368 | utr-variant-3-prime | Hecw1 | Mm_Celera | 13:14227760 | AGACATAATTTCAAT[G/T]TTCTCATGGATGAAG | 94253 |
rs29708666 | snp | C/G | 0.188366 | 0.242283 | intron-variant | Hecw1 | Mm_Celera | 13:14358336 | AACCTTAGCAAACAA[C/G]TGTTCAAGTACAAAT | 94253 |
rs29714975 | snp | G/T | 0.375 | 0.216506 | intron-variant | Hecw1 | Mm_Celera | 13:14358714 | CAGATTCCCACCACC[G/T]CATAGAGCCCCAATC | 94253 |
rs29724966 | snp | A/C | 0.498615 | 0.0262793 | intron-variant | Hecw1 | Mm_Celera | 13:14319067 | AGCTGGTGGGACAGG[A/C]AATCTCAGAGAAGCC | 94253 |
rs29725589 | snp | A/G | 0.375 | 0.216506 | intron-variant | Hecw1 | Mm_Celera | 13:14269725 | TGGAATTTTTTTTCT[A/G]AACACACAACTAAAA | 94253 |
rs29725757 | snp | C/T | 0.375 | 0.216506 | intron-variant | Hecw1 | Mm_Celera | 13:14277393 | CGGGGACTCCATGGA[C/T]GAGCTGGAGGAGGGA | 94253 |
rs29726475 | snp | C/G | 0.375 | 0.216506 | intron-variant | Hecw1 | Mm_Celera | 13:14359603 | CCCCTGCCCTGCTCC[C/G]CTACCCACCCACTCC | 94253 |
rs29731206 | snp | A/G | 0.375 | 0.216506 | intron-variant | Hecw1 | Mm_Celera | 13:14283775 | TCTGTGGGTTGTATC[A/G]TGGGCATTGTGAGCT | 94253 |
rs29731567 | snp | C/T | 0.375 | 0.216506 | intron-variant | Hecw1 | Mm_Celera | 13:14263510 | AACCCTGAGATTCCA[C/T]GTCAGACCAGTCAAA | 94253 |
rs29759113 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Hecw1 | Mm_Celera | 13:14313427 | TTCAAAAAGGAAACG[A/G]GCATAGCTGTTGCCT | 94253 |
rs29759664 | snp | G/T | 0.375 | 0.216506 | intron-variant | Hecw1 | Mm_Celera | 13:14278615 | CTACTTCATCTATGT[G/T]TAGATGGAAGATGAA | 94253 |
rs29770870 | snp | C/T | 0.465374 | 0.126941 | intron-variant | Hecw1 | Mm_Celera | 13:14358672 | TCTTTCCAAACACCA[C/T]TTTATACTTCAAGAA | 94253 |
rs29772773 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Hecw1 | Mm_Celera | 13:14237462 | AGTGTTGGTCTTCCT[A/G]TGGGGTTACCATCCA | 94253 |
rs29779280 | snp | G/T | 0.375 | 0.216506 | intron-variant | Hecw1 | Mm_Celera | 13:14268501 | CTTCCGGTAGTACTA[G/T]GTCCAGTTTTCTGAG | 94253 |
rs29781335 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Hecw1 | Mm_Celera | 13:14346891 | AATATATCACTCTGG[A/G]TTGCTTTTGAGGGGC | 94253 |
rs29781441 | snp | A/G | 0.188366 | 0.242283 | intron-variant | Hecw1 | Mm_Celera | 13:14358462 | TCTAGTTGGCCAAGC[A/G]TTTTACAGCTTTCTT | 94253 |
rs29804775 | snp | A/C | 0.465374 | 0.126941 | intron-variant | Hecw1 | Mm_Celera | 13:14346926 | AAGCGGACAGATGAG[A/C]TATAAAACACTATGC | 94253 |
rs29822269 | snp | C/T | 0.375 | 0.216506 | intron-variant | Hecw1 | Mm_Celera | 13:14333775 | CCCCAATACTTCAAC[C/T]GGCAGGCCATGCCTA | 94253 |
rs29827236 | snp | A/G | 0.475309 | 0.108333 | intron-variant | Hecw1 | Mm_Celera | 13:14311484 | CAGAAACTTAGGTAT[A/G]TTAACATTTGTTTAT | 94253 |
rs29829262 | snp | A/G | 0.484429 | 0.0868505 | intron-variant | Hecw1 | Mm_Celera | 13:14310147 | TCTACAGAGTCCCAG[A/G]TGATTGGTTTGTACT | 94253 |
rs29829696 | snp | A/G | 0.5 | 0 | intron-variant | Hecw1 | Mm_Celera | 13:14312014 | AGGAGAAAGAAGAAG[A/G]AAGAGAAAGAGGAAA | 94253 |
rs29829806 | snp | C/T | 0.5 | 0 | intron-variant | Hecw1 | Mm_Celera | 13:14251189 | TTGTTGGGAATTGAA[C/T]TCAGGACCTCTGGAA | 94253 |
rs29831433 | snp | C/T | 0.375 | 0.216506 | intron-variant | Hecw1 | Mm_Celera | 13:14263565 | AACAGCAGATGCTGG[C/T]GAGGATGTGGAGAAA | 94253 |
rs29831636 | snp | G/T | 0.277778 | 0.248452 | intron-variant | Hecw1 | Mm_Celera | 13:14344671 | AAAAAATAATTTTCA[G/T]TTCACAGAAGAGTTC | 94253 |
rs29842261 | snp | C/T | 0.290657 | 0.246672 | intron-variant | Hecw1 | Mm_Celera | 13:14346531 | GGAGGATTAATGTTC[C/T]GGACATAAGATGCAA | 94253 |
rs29850310 | snp | G/T | 0.375 | 0.216506 | intron-variant | Hecw1 | Mm_Celera | 13:14275578 | GCTCCTCAGATTCTT[G/T]CTCAGTCATGCTCAT | 94253 |
rs29852252 | snp | A/G | 0.498615 | 0.0262793 | intron-variant | Hecw1 | Mm_Celera | 13:14321516 | TGCTTAAGTTATAGA[A/G]GTGTTATGAAAACCA | 94253 |
rs29868064 | snp | C/T | 0.46875 | 0.121031 | intron-variant | Hecw1 | Mm_Celera | 13:14317947 | ACATTTAACAGTGAA[C/T]GCTGTTTAACTCTAC | 94253 |
rs29868837 | snp | G/T | 0.375 | 0.216506 | intron-variant | Hecw1 | Mm_Celera | 13:14315338 | TTGTGACCTGTGGGG[G/T]GATTAGTTAGTGGAG | 94253 |
rs29897196 | snp | A/G | 0.375 | 0.216506 | intron-variant | Hecw1 | Mm_Celera | 13:14309638 | TCCAGGCTGAAACTG[A/G]GTCATTATTAATTCT | 94253 |
rs29900756 | snp | G/T | 0.197531 | 0.244432 | intron-variant | Hecw1 | Mm_Celera | 13:14348641 | GTCCTTTGGTCCTTC[G/T]AGTAGACCTTGGAAT | 94253 |
rs29910288 | snp | C/T | 0.375 | 0.216506 | intron-variant | Hecw1 | Mm_Celera | 13:14245700 | CCCAGGGGCTATGGC[C/T]TGCTTTCCTGGTCCA | 94253 |
rs29917563 | snp | A/G | 0.375 | 0.216506 | intron-variant | Hecw1 | Mm_Celera | 13:14288584 | CATCTATAAAAGCTC[A/G]AAGATCCGGGGTAGA | 94253 |
rs29929484 | snp | C/T | 0.290657 | 0.246672 | intron-variant | Hecw1 | Mm_Celera | 13:14238336 | AGGATTGGGAAGGAC[C/T]CATTGGTTACAGCTC | 94253 |
rs29959696 | snp | A/G | 0.5 | 0 | intron-variant | Hecw1 | Mm_Celera | 13:14273299 | ACAGAGTCTTACACA[A/G]CATCATTCTACAAAA | 94253 |
rs29959894 | snp | A/G | 0.5 | 0 | intron-variant | Hecw1 | Mm_Celera | 13:14360531 | GTTTTCTGAGGAACC[A/G]CCAGACTGACTTCTA | 94253 |
rs29963786 | snp | C/T | 0.375 | 0.216506 | intron-variant | Hecw1 | Mm_Celera | 13:14331971 | CATGATATGTACTCA[C/T]TGATAAGTCAATATC | 94253 |
rs29969653 | snp | A/G | 0.265928 | 0.249492 | intron-variant | Hecw1 | Mm_Celera | 13:14237163 | TATTTCAAATACGGG[A/G]TCATTTTAAAATTTA | 94253 |
rs29975943 | snp | A/G | 0.5 | 0 | intron-variant | Hecw1 | Mm_Celera | 13:14287821 | GAGGGGGAGGGCATA[A/G]GGGCCTTTTGGGATA | 94253 |
rs29976901 | snp | C/T | 0.375 | 0.216506 | intron-variant | Hecw1 | Mm_Celera | 13:14359689 | AGGGTCCTCTCTTCC[C/T]AATGATGCCCAACTA | 94253 |
rs29993517 | snp | C/T | 0.188366 | 0.242283 | intron-variant | Hecw1 | Mm_Celera | 13:14319556 | CTGGCAATAGATGTG[C/T]CAGAATATGTTGGAG | 94253 |
rs30001208 | snp | C/T | 0.207612 | 0.24638 | intron-variant | Hecw1 | Mm_Celera | 13:14364345 | TTGCAGTGATGCCTT[C/T]AGCTCTTTGGTTAGA | 94253 |
rs30005473 | snp | C/T | 0.375 | 0.216506 | intron-variant | Hecw1 | Mm_Celera | 13:14318148 | AAAACAAAAATATTT[C/T]CTTACAATCTAGTAT | 94253 |
rs30013856 | snp | C/T | 0.375 | 0.216506 | intron-variant | Hecw1 | Mm_Celera | 13:14329369 | GGAGCTAAATGACAT[C/T]AAAACAAAATGGACC | 94253 |
rs30026497 | snp | G/T | 0.48 | 0.0979796 | intron-variant | Hecw1 | Mm_Celera | 13:14329709 | GAAGGAAGACCAATA[G/T]TGTATATGCTTCAAT | 94253 |
rs30046385 | snp | C/T | 0.197531 | 0.244432 | intron-variant | Hecw1 | Mm_Celera | 13:14352354 | ATAAAAAGACATGTT[C/T]GAGAATGTGGGTATG | 94253 |
rs30046391 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Hecw1 | Mm_Celera | 13:14346871 | AGCTTAATATAGACA[A/G]TAAAAATATATCACT | 94253 |
rs30059580 | snp | A/G | 0.375 | 0.216506 | intron-variant | Hecw1 | Mm_Celera | 13:14289714 | CATATCCAAACTTAT[A/G]GGACACAATGAAAAC | 94253 |
rs30059757 | snp | C/T | 0.492188 | 0.0620098 | intron-variant | Hecw1 | Mm_Celera | 13:14264729 | CTCAGAAATGTACAC[C/T]ACATATAAAGTAAAT | 94253 |
rs30061021 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Hecw1 | Mm_Celera | 13:14273070 | CTACAGACTAATAAA[C/T]GAAGTCTCCTTCCCC | 94253 |
rs30065277 | snp | C/G | 0.32 | 0.24 | intron-variant | Hecw1 | Mm_Celera | 13:14436780 | GATGGTAGAGCTGAA[C/G]TGGGGTTGTACAAGC | 94253 |
rs30091270 | snp | A/G | 0.375 | 0.216506 | intron-variant | Hecw1 | Mm_Celera | 13:14341050 | TAGTTTTAGATATTT[A/G]AACACTCATCCTCAG | 94253 |
rs30095197 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Hecw1 | Mm_Celera | 13:14246002 | CTTAGAAGAGCTACA[A/G]TTTATTTACTTATTT | 94253 |
rs31183163 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Hecw1 | Mm_Celera | 13:14254811 | AGTCCTTCGAGTTTC[C/T]TCAGTTGAGAATTCA | 94253 |
rs31405140 | snp | A/G | 0.5 | 0 | intron-variant | Hecw1 | Mm_Celera | 13:14289840 | CTCTTAGGTGTATTA[A/G]CTTCTTTTTGTTCTA | 94253 |
rs31645214 | snp | A/T | 0.345679 | 0.230967 | intron-variant | Hecw1 | Mm_Celera | 13:14284225 | CAGTCGGAATGACTA[A/T]GATCAAAACTCAGGT | 94253 |
rs31665540 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Hecw1 | Mm_Celera | 13:14477407 | CATTGTAAAAATGGC[C/G]ATCTTGCCAAAAGCA | 94253 |
rs33846184 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Hecw1 | Mm_Celera | 13:14346777 | TCCCCTCGCACCCAC[A/G]AATAACTGAATCCCG | 94253 |
rs33847572 | snp | C/T | 0.32 | 0.24 | missense | Hecw1 | GRCm38.p3 | 13:14317289 | TGCTGTTTCCCACCA[C/T]ACTATTCATGATGCT | 94253 |
rs33851115 | snp | A/G/T | 0.444444 | 0.157135 | intron-variant | Hecw1 | Mm_Celera | 13:14261168 | GACCAGAGATTAATC[A/G/T]GCGGGAATCGGATCC | 94253 |
rs45639715 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Hecw1 | Mm_Celera | 13:14454031 | CAAAGAAGGCTAAAA[C/T]GGAAGCTTAGAGGCT | 94253 |
rs45640337 | snp | A/C | 0.473373 | 0.11227 | intron-variant | Hecw1 | Mm_Celera | 13:14422239 | CACTAATACTATAGT[A/C]CTAATGGCATGGGAA | 94253 |
rs45654604 | snp | C/T | 0.165289 | 0.235211 | intron-variant | Hecw1 | Mm_Celera | 13:14233287 | CTTCACTATCAAAAT[C/T]TATCATGAAGATAGA | 94253 |
rs45667260 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Hecw1 | Mm_Celera | 13:14319959 | AGGCATAGTCCATAG[C/T]TGGTTATTTACTCTA | 94253 |
rs45668607 | snp | A/T | 0.408163 | 0.193609 | intron-variant | Hecw1 | Mm_Celera | 13:14325150 | ATAGGTGATTTTTTT[A/T]AAACTAAGCTCCTGC | 94253 |
rs45668924 | snp | C/T | | | intron-variant | Hecw1 | Mm_Celera | 13:14475215 | GAAGGACACTTCATA[C/T]TCATCAAAGAAAATA | 94253 |
rs45669248 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Hecw1 | Mm_Celera | 13:14320488 | AAAGTGCTGAAGATG[A/G]CCTTTGTGTCCTGTA | 94253 |
rs45669923 | snp | C/T | 0.459184 | 0.136902 | intron-variant | Hecw1 | Mm_Celera | 13:14252585 | AGGCAGGAGGCACTG[C/T]AACCTTTTGCTGCTG | 94253 |
rs45671493 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Hecw1 | Mm_Celera | 13:14454826 | TGCCAATGCAGTCAT[A/G]CTCCATGTAAAGATA | 94253 |
rs45680395 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Hecw1 | Mm_Celera | 13:14281914 | ATTCTATGCCACACT[A/G]ATGGACTTTCCACTT | 94253 |
rs45685107 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Hecw1 | Mm_Celera | 13:14321018 | ACTGGGAAAACCAAA[C/T]TCCCTTGCTCAGGTT | 94253 |
rs45688630 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Hecw1 | Mm_Celera | 13:14252274 | GGTCTGGAGCTGAGC[A/G]TCAATATCTGATTGT | 94253 |
rs45695784 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Hecw1 | Mm_Celera | 13:14495451 | AATGGACCATAGACT[A/G]AAATCTCTATACTTG | 94253 |
rs45701547 | snp | A/G | | | intron-variant | Hecw1 | Mm_Celera | 13:14242718 | CCCTGATTTTAGTAG[A/G]ATTGCTTCAAGTTTT | 94253 |
rs45705776 | snp | A/C | | | intron-variant | Hecw1 | Mm_Celera | 13:14363934 | GGGAGGGAAGAGTGA[A/C]CATGGCAGCACTTTC | 94253 |
rs45710985 | snp | A/G | 0.32 | 0.24 | intron-variant | Hecw1 | Mm_Celera | 13:14354791 | GACAGCATTCAATGG[A/G]AGGTAGAATTGATGA | 94253 |
rs45717888 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Hecw1 | Mm_Celera | 13:14349345 | GCAACCCTGGCACAT[A/C]CTTTTTGTTCAGAAA | 94253 |
rs45718164 | snp | A/G | | | intron-variant | Hecw1 | GRCm38.p3 | 13:14240899 | TGGATATGTAAACAG[A/G]ACTCAGAATTTTGCT | 94253 |
rs45721711 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | Hecw1 | Mm_Celera | 13:14395470 | TAGCCTCTTATTTTT[A/G]TGCCCGGTTCCCTGG | 94253 |
rs45722956 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Hecw1 | Mm_Celera | 13:14251606 | CTGGTGGAAAATCTG[A/G]ATGAAAAATCTGTGG | 94253 |
rs45727714 | snp | C/T | 0.444444 | 0.157135 | utr-variant-3-prime | Hecw1 | GRCm38.p3 | 13:14226559 | AGCCCAGTAATATGA[C/T]GTCTCCTGTTATTGA | 94253 |
rs45727898 | snp | A/T | | | intron-variant | Hecw1 | GRCm38.p3 | 13:14242000 | TGGAGGAAGTTAAAA[A/T]AATTATCAGATCCTA | 94253 |
rs45732899 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Hecw1 | Mm_Celera | 13:14487578 | CATGCATACATGAAA[A/G]ATGCTTGAAGGGCAT | 94253 |
rs45734708 | snp | A/G | | | intron-variant | Hecw1 | Mm_Celera | 13:14236381 | GAGGCTTTTAAAAGC[A/G]ATAAATTGGGCTCTG | 94253 |
rs45738067 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Hecw1 | Mm_Celera | 13:14294209 | CTCAGAAAACATTTT[C/T]ATCCTTTCTATTAGA | 94253 |
rs45738838 | snp | A/C | 0.336735 | 0.234472 | intron-variant | Hecw1 | Mm_Celera | 13:14298976 | TCACCCCAGCAGTAT[A/C]TATCTCTCAATTTGG | 94253 |
rs45738954 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Hecw1 | Mm_Celera | 13:14348700 | AATTCAGTAATAAAA[G/T]AAGTCATTGGGACTT | 94253 |
rs45740164 | snp | C/T | 0.124444 | 0.216185 | intron-variant, upstream-variant-2KB | Hecw1 | Mm_Celera | 13:14458048 | TATCTTGTGTGGGAA[C/T]AGTGTAGAAGGTGAC | 94253 |
rs45745468 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Hecw1 | Mm_Celera | 13:14235337 | TTCTTAACTTATCTG[C/T]GTAGAATTTCCAGAG | 94253 |
rs45753518 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Hecw1 | Mm_Celera | 13:14321314 | TCCCCTTGGCCCACA[C/G]TGGGCAAAGCATTAG | 94253 |
rs45758694 | snp | A/G | | | intron-variant | Hecw1 | Mm_Celera | 13:14239558 | ACCCAAATTCCTCCT[A/G]AGAGAACTGGTTTCC | 94253 |
rs45766219 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Hecw1 | Mm_Celera | 13:14425351 | GTGCTGTATCAGAAT[G/T]ATAATCTTAAATAGA | 94253 |
rs45769979 | snp | A/C | 0.142012 | 0.225474 | intron-variant | Hecw1 | Mm_Celera | 13:14374083 | TATAACAACAAAATG[A/C]ATCATAGTTCGGCTC | 94253 |
rs45777155 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Hecw1 | Mm_Celera | 13:14360727 | TTTAGAAGCTTGATC[A/G]TCAATCTATCTTCCT | 94253 |
rs45781952 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Hecw1 | Mm_Celera | 13:14380321 | GCCCCTCTCTGCCCT[A/G]CTAAGAGCCTTTTTC | 94253 |
rs45786650 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Hecw1 | Mm_Celera | 13:14357256 | ATAAAATGAAGCTGA[A/G]TCAGGGCAATCTAGG | 94253 |
rs45799227 | snp | C/T | 0.165289 | 0.235211 | intron-variant | Hecw1 | Mm_Celera | 13:14466490 | CACTCCACCCATCCT[C/T]TAGAGGTGATTCTCT | 94253 |
rs45801049 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Hecw1 | Mm_Celera | 13:14406377 | CACTCAGATACATTC[C/T]TGCTCTTGGAAACGT | 94253 |
rs45817869 | snp | G/T | 0.32 | 0.24 | intron-variant | Hecw1 | Mm_Celera | 13:14376919 | GTGAATAGTATTAAA[G/T]CTGGTGTTGTGCATC | 94253 |
rs45819638 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Hecw1 | Mm_Celera | 13:14286117 | ACACTGGCCATCATA[A/G]TCATCATACCTATTC | 94253 |
rs45822743 | snp | C/T | 0.473373 | 0.11227 | intron-variant | Hecw1 | Mm_Celera | 13:14421367 | TCTTCTGCATTGTCA[C/T]CACCACCACTGATTA | 94253 |
rs45823139 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Hecw1 | Mm_Celera | 13:14491387 | TATTGTGGTACAGAG[A/G]TTTATAGAATCTTTC | 94253 |
rs45835999 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Hecw1 | Mm_Celera | 13:14425483 | GAAGTGAGAAAGGAG[C/T]CAAGGTTCCCTAGGT | 94253 |
rs45836230 | snp | A/G | 0.426035 | 0.177515 | intron-variant | Hecw1 | Mm_Celera | 13:14482936 | GACAGTAAACACTGC[A/G]GTTCTAGCAGAGGGT | 94253 |
rs45836965 | snp | A/G | | | intron-variant | Hecw1 | Mm_Celera | 13:14284542 | ATGGGACCTCATAAA[A/G]TTGAAATGCTTCTGT | 94253 |
rs45840460 | snp | A/G | 0.260355 | 0.249785 | intron-variant, utr-variant-5-prime | Hecw1 | Mm_Celera | 13:14454902 | TCAATACCTACAGAG[A/G]TTCCAGGGATGAAAA | 94253 |
rs45842351 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Hecw1 | Mm_Celera | 13:14247732 | GTTGAGTAAACAAAT[A/G]TGGTTTCCATACTCC | 94253 |
rs45847118 | snp | G/T | 0.426035 | 0.177515 | intron-variant | Hecw1 | Mm_Celera | 13:14371837 | CTCTGCTTTTACATG[G/T]TTCCTAAGCACCTTT | 94253 |
rs45855215 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Hecw1 | Mm_Celera | 13:14264293 | AGTGAGGACTTTCAG[A/G]TATGGGGTCTGAGAA | 94253 |
rs45864765 | snp | C/T | | | intron-variant | Hecw1 | Mm_Celera | 13:14246427 | ATTCTTATTGTATAC[C/T]TAAAAAGAAGTACAG | 94253 |
rs45870156 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Hecw1 | Mm_Celera | 13:14250725 | ACCAATAGTTAGATT[G/T]TTTTCTTAGATTAAA | 94253 |
rs45874447 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Hecw1 | Mm_Celera | 13:14492100 | TCCAGTTAGTTTCTC[C/T]ATCCCTAATTCAATG | 94253 |
rs45875543 | snp | C/G/T | | | intron-variant | Hecw1 | GRCm38.p3 | 13:14325618 | TGAATGGGAGAAAAT[C/G/T]TTTGCCAACTATACA | 94253 |
rs45879363 | snp | C/T | 0.489796 | 0.070696 | intron-variant | Hecw1 | Mm_Celera | 13:14315182 | TGGGTAGGTGGGAGA[C/T]CTGGACCATGATGAC | 94253 |
rs45890464 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Hecw1 | Mm_Celera | 13:14379703 | AATCTTTGTGTGTCA[C/T]TCTTCCACTTTATTC | 94253 |
rs45891742 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Hecw1 | Mm_Celera | 13:14495111 | TTAGAAATATAGGGT[C/T]GTGGCACTAAATGTG | 94253 |
rs45891867 | snp | C/T | 0.124444 | 0.216185 | synonymous-codon | Hecw1 | Mm_Celera | 13:14230751 | CAATCGGTTGAAGCA[C/T]GTATGTGCCCTGAGT | 94253 |
rs45893052 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Hecw1 | Mm_Celera | 13:14395159 | CAAAGCTGTCATAAA[C/T]CCTCTGGAAATTTTT | 94253 |
rs45910753 | snp | C/T | 0.444444 | 0.157135 | utr-variant-3-prime | Hecw1 | GRCm38.p3 | 13:14227810 | ACTGGCTTTTGAGCT[C/T]CTCTCCCCTTTGTTT | 94253 |
rs45911553 | snp | A/G | 0.124444 | 0.216185 | intron-variant, upstream-variant-2KB | Hecw1 | Mm_Celera | 13:14458216 | TGTACAAGGCATGGC[A/G]TTCCTTATGTCCCAT | 94253 |
rs45913314 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Hecw1 | Mm_Celera | 13:14249978 | CTTAACTGTAGTTTG[C/T]CCAGGTAATTTCTCT | 94253 |
rs45916377 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Hecw1 | Mm_Celera | 13:14378514 | GTTTCTCAGTCCTCT[A/G]TAATGTCTATTAAGG | 94253 |
rs45917248 | snp | A/G | 0.32 | 0.24 | intron-variant | Hecw1 | Mm_Celera | 13:14359220 | TCAGTGCCATTCCAC[A/G]CTGGGTACACTGTCT | 94253 |
rs45927790 | snp | C/T | 0.459184 | 0.136902 | intron-variant | Hecw1 | Mm_Celera | 13:14480330 | GCATCAGGTTCATTG[C/T]GTCCCACATCCTCAG | 94253 |
rs45929129 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Hecw1 | Mm_Celera | 13:14361804 | GAAATACAACTGGAG[A/G]TTCTTCTTTGTAAGT | 94253 |
rs45932507 | snp | C/T | 0.35503 | 0.226867 | intron-variant | Hecw1 | Mm_Celera | 13:14427210 | TAATAACTGTCTCTG[C/T]TATTATTTCTAATCA | 94253 |
rs45941212 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Hecw1 | Mm_Celera | 13:14354594 | TATCAAGAAATAAGG[A/G]CAACAATAGCATAGT | 94253 |
rs45954179 | snp | A/C/G | 0.197531 | 0.244432 | intron-variant | Hecw1 | GRCm38.p3 | 13:14372354 | AGTTGTATAAAATAT[A/C/G]TAAAAGTCTTCAAAA | 94253 |
rs45954190 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Hecw1 | Mm_Celera | 13:14395619 | AACCATTGTGGATAT[C/T]ATGATAGGGTTCCAG | 94253 |
rs45954931 | snp | C/G | 0.497778 | 0.0332592 | intron-variant | Hecw1 | Mm_Celera | 13:14378444 | AAGAATGGTTCCTGT[C/G]GGGTAAGGTAGTCAT | 94253 |
rs45955164 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Hecw1 | Mm_Celera | 13:14463957 | TAGGAAGTAGAGACG[A/G]AATGATGATTATCAC | 94253 |
rs45959225 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Hecw1 | Mm_Celera | 13:14340490 | AATTTTGGGCTGGAG[A/G]GTAGGCATTCTCCCA | 94253 |
rs45964140 | snp | C/T | | | intron-variant | Hecw1 | Mm_Celera | 13:14448215 | AGCAGCTTGACAACA[C/T]ACCTAAAAGCTCTAG | 94253 |
rs45967974 | snp | A/G | 0.124444 | 0.216185 | downstream-variant-500B | Hecw1 | Mm_Celera | 13:14226184 | ATAAAGGACACTTAG[A/G]AAATGAGGCACATAT | 94253 |
rs45969443 | snp | C/G | 0.244898 | 0.249948 | intron-variant | Hecw1 | Mm_Celera | 13:14444823 | TTCTCTGTGTAGGTC[C/G]GGATGGCCTTGAACT | 94253 |
rs45986462 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Hecw1 | Mm_Celera | 13:14481183 | ATGGAATAAGGAATT[C/T]GAAAGAAAAACCCCT | 94253 |
rs45987753 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Hecw1 | Mm_Celera | 13:14235000 | GGAGCTGCTTTAAGG[C/T]TCTGTTGAAGAAGCT | 94253 |
rs45993284 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Hecw1 | Mm_Celera | 13:14344078 | ACATGAAAATAGAAA[C/T]CCAAGGGTAGCACTT | 94253 |
rs46006140 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Hecw1 | Mm_Celera | 13:14364217 | ATATGCCTTAAACTG[C/T]ATCAAAGGAAAACTA | 94253 |
rs46006473 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Hecw1 | Mm_Celera | 13:14482133 | AGACAAAGGCAAATT[C/T]CCCAACTAGAGCCAA | 94253 |
rs46007154 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Hecw1 | Mm_Celera | 13:14304471 | CAGGTGACTACATGT[A/G]ACTAGGAGTCCAACA | 94253 |
rs46009376 | snp | C/T | 0.124444 | 0.216185 | intron-variant, upstream-variant-2KB | Hecw1 | Mm_Celera | 13:14459214 | GATTCTTTTGTCAAA[C/T]ATATCACAGGAATGG | 94253 |
rs46010788 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Hecw1 | Mm_Celera | 13:14319090 | GAGAAGCCATTGTAA[C/T]AGGGAGTGAAGGTCC | 94253 |
rs46018292 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Hecw1 | Mm_Celera | 13:14352167 | ATAGAATAAGCCTTA[A/G]AGACTGTAAATCAAA | 94253 |
rs46025261 | snp | C/T | 0.375 | 0.216506 | intron-variant | Hecw1 | Mm_Celera | 13:14371265 | TACAAATGTGGTACC[C/T]CTTGTACAGGATACC | 94253 |
rs46031495 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Hecw1 | Mm_Celera | 13:14489335 | CCAGCCACTGGGCAG[C/T]AGGAATTCTGCCATG | 94253 |
rs46032171 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Hecw1 | Mm_Celera | 13:14357459 | TTAAATAAATCCATT[A/T]CTTGGCATCCTATCT | 94253 |
rs46033161 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Hecw1 | Mm_Celera | 13:14306362 | ACTAAGTCTACTGTG[A/G]CCTATGTGGCAATTT | 94253 |
rs46048670 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Hecw1 | Mm_Celera | 13:14278647 | ATCAGCACAGCTCTC[C/T]TGTGAGGACATCTGT | 94253 |
rs46049171 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Hecw1 | Mm_Celera | 13:14460074 | AACACAATGTAGTGC[C/T]ATTAAAGCACCATGT | 94253 |
rs46050148 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Hecw1 | Mm_Celera | 13:14251299 | ACTACAGCTCATAAC[C/T]TATAGGCAATAACAT | 94253 |
rs46061264 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Hecw1 | Mm_Celera | 13:14480238 | AGTCTCACACTTTTA[C/T]ATCCACACTTAAGAG | 94253 |
rs46064908 | snp | G/T | 0.244898 | 0.249948 | intron-variant | Hecw1 | Mm_Celera | 13:14479340 | CACCCACTGTTTATA[G/T]GAAAAAATTCAAATC | 94253 |
rs46080525 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Hecw1 | Mm_Celera | 13:14281977 | AAACCAGCTTTCAGA[A/G]CAGGAGCTGCAGCAG | 94253 |
rs46085373 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Hecw1 | Mm_Celera | 13:14432247 | CTATATGTGGTGATG[G/T]TTTTCTATTTTTTAT | 94253 |
rs46087073 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Hecw1 | Mm_Celera | 13:14493983 | CAAGTAAAAAGAAGA[A/G]GCTCTGAACAACATT | 94253 |
rs46090794 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Hecw1 | Mm_Celera | 13:14294098 | GGAGCTATGACACTG[A/G]CAAGGTGACGTGAAC | 94253 |
rs46092529 | snp | C/T | 0.165289 | 0.235211 | intron-variant | Hecw1 | Mm_Celera | 13:14429729 | TCTGGCAAACCTAAC[C/T]ACATGGGACCTTTTA | 94253 |
rs46092609 | snp | C/T | | | intron-variant | Hecw1 | Mm_Celera | 13:14257683 | TGAGGTCTCATTTGT[C/T]GAGTCTTGATCTTAC | 94253 |
rs46093858 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Hecw1 | Mm_Celera | 13:14232879 | ACCATCTCATCCGTG[A/G]ACATTTCTCAGGACA | 94253 |
rs46097006 | snp | G/T | 0.197531 | 0.244432 | intron-variant | Hecw1 | Mm_Celera | 13:14504288 | TGAAGGGAGCAGATA[G/T]AAATTCTTCAGCAAA | 94253 |
rs46098544 | snp | A/G | 0.375 | 0.216506 | intron-variant | Hecw1 | Mm_Celera | 13:14370935 | TCTAAGTGGCAGAAA[A/G]TACGAAAAAATTGTA | 94253 |
rs46107979 | snp | C/T | 0.426035 | 0.177515 | intron-variant | Hecw1 | Mm_Celera | 13:14372609 | ATACCTTGCTTTTCT[C/T]TACCCTGCTTGTACT | 94253 |
rs46108046 | snp | C/T | 0.165289 | 0.235211 | intron-variant | Hecw1 | Mm_Celera | 13:14273771 | CTTATACCATTTCTA[C/T]CACTATCTTTCTACC | 94253 |
rs46108970 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Hecw1 | Mm_Celera | 13:14415155 | GATTTTGGTTAAACT[A/C]TTTGCCACGACTTAC | 94253 |
rs46117264 | snp | C/G | 0.231111 | 0.249285 | intron-variant, upstream-variant-2KB | Hecw1 | Mm_Celera | 13:14458044 | CCAGTATCTTGTGTG[C/G]GAATAGTGTAGAAGG | 94253 |
rs46119998 | snp | C/T | | | intron-variant | Hecw1 | Mm_Celera | 13:14433555 | TGAATATCCAGCTGT[C/T]CCTTATTTGGCAACT | 94253 |
rs46128481 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Hecw1 | Mm_Celera | 13:14467568 | TGTCCTTCCAGTTGT[A/G]CCTTGCTTGTCACAA | 94253 |
rs46130813 | snp | A/G | 0.459184 | 0.136902 | intron-variant | Hecw1 | Mm_Celera | 13:14424136 | ATGACCACAGACTTG[A/G]TGAACTCTAAGCTAT | 94253 |
rs46135255 | snp | A/G | | | intron-variant | Hecw1 | Mm_Celera | 13:14239647 | CCAGCTAACACCAGG[A/G]ATAACTAGATGGCTA | 94253 |
rs46145304 | snp | C/T | 0.375 | 0.216506 | intron-variant | Hecw1 | Mm_Celera | 13:14374662 | CTAGCAGCCTTATTT[C/T]TTTATCACTTCCTCC | 94253 |
rs46151262 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Hecw1 | Mm_Celera | 13:14506969 | CCCTTACAGATCTTC[C/T]TCAGAGGCACCGCCT | 94253 |
rs46153575 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Hecw1 | Mm_Celera | 13:14426620 | TGGTTCTTCTGGACC[C/T]AGCATGGCCATGGCT | 94253 |
rs46154619 | snp | A/T | | | intron-variant | Hecw1 | Mm_Celera | 13:14339104 | AATCATATCTTATGA[A/T]GCCAATAGAGGATTT | 94253 |
rs46155252 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Hecw1 | Mm_Celera | 13:14454785 | ATCTAGAGCCTCATA[C/T]AGATAGAATCTTCCA | 94253 |
rs46161300 | snp | C/T | 0.426035 | 0.177515 | intron-variant | Hecw1 | Mm_Celera | 13:14252455 | AGAAGGCAGCAGCCA[C/T]ACCCATCCTGCTGTG | 94253 |
rs46164700 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Hecw1 | Mm_Celera | 13:14332822 | TTGATCTTGACCATT[C/T]TGAGTGGTCTCATGG | 94253 |
rs46179109 | snp | C/T | 0.32 | 0.24 | intron-variant | Hecw1 | Mm_Celera | 13:14352945 | GTGGCCTTTTCCCAG[C/T]TGCATGGATATTGCC | 94253 |
rs46182320 | snp | A/C | 0.408163 | 0.193609 | intron-variant, utr-variant-5-prime | Hecw1 | Mm_Celera | 13:14456887 | AGAACACAACCACGA[A/C]CTCTGTACATCACTG | 94253 |
rs46185931 | snp | A/G | 0.32 | 0.24 | intron-variant | Hecw1 | Mm_Celera | 13:14346905 | GGTTGCTTTTGAGGG[A/G]CAATCAAGCGGACAG | 94253 |
rs46210131 | snp | A/C | | | intron-variant | Hecw1 | Mm_Celera | 13:14510949 | ACCATCAAGGAAAAA[A/C]CTCCTGGATTATATC | 94253 |
rs46212403 | snp | A/C | | | intron-variant | Hecw1 | GRCm38.p3 | 13:14242076 | GGACAATTTTCTAGA[A/C]AGATACCAAATACCA | 94253 |
rs46216933 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Hecw1 | Mm_Celera | 13:14352462 | CTAAGTTTTCCTGTT[C/T]ACGAAAGCAATTCTT | 94253 |
rs46221496 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Hecw1 | Mm_Celera | 13:14315033 | GAGATGCTTGTGTCT[C/T]TCAATCCGACTAATA | 94253 |
rs46236280 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Hecw1 | Mm_Celera | 13:14387015 | ACCCAAGATCGAAAT[G/T]GTCAAATTATAATAG | 94253 |
rs46237697 | snp | A/G | | | intron-variant | Hecw1 | Mm_Celera | 13:14433913 | GTGGGGGGGGATTTG[A/G]CAGGGATTCTGAGAG | 94253 |
rs46238428 | snp | C/G | | | intron-variant | Hecw1 | Mm_Celera | 13:14433856 | TATTGGTTAGTCTCT[C/G]TCTGGGAAGGGAGTT | 94253 |
rs46243729 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Hecw1 | Mm_Celera | 13:14344706 | AAAAAGTCAAGATTT[C/T]CTGTAACTCCTTACT | 94253 |
rs46264813 | snp | A/C | 0.426035 | 0.177515 | intron-variant | Hecw1 | Mm_Celera | 13:14370881 | ATTATAGTCTATTCC[A/C]TGTTTGTCGTATTTG | 94253 |
rs46269687 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Hecw1 | Mm_Celera | 13:14230893 | ACTGCAAATGGCAAA[A/G]CATGGCTGTTGAGAT | 94253 |
rs46273207 | snp | C/G | 0.497778 | 0.0332592 | intron-variant | Hecw1 | Mm_Celera | 13:14380719 | TATGGAGGAAAATAT[C/G]TTTAGGACTCAGAGT | 94253 |
rs46280216 | snp | C/T | 0.260355 | 0.249785 | intron-variant, utr-variant-5-prime | Hecw1 | Mm_Celera | 13:14455920 | CCTCTGCATCCCCTG[C/T]AGCCAGGCTCTGATT | 94253 |
rs46280556 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Hecw1 | Mm_Celera | 13:14278520 | TGTATAAAACCAGGA[C/T]ACAATAGCATTATTA | 94253 |
rs46286112 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Hecw1 | Mm_Celera | 13:14263970 | ATTCCTGGCTAACTA[C/T]TCCAAATTCAGTTTC | 94253 |
rs46323705 | snp | A/G | 0.32 | 0.24 | intron-variant | Hecw1 | Mm_Celera | 13:14315656 | ACTGATCTTTAATGT[A/G]TTTTAGGAAGTCAAA | 94253 |
rs46328724 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Hecw1 | Mm_Celera | 13:14285385 | CAGCTAATGGGCACC[C/T]CATAATAATCACTCA | 94253 |
rs46338026 | snp | C/T | 0.124444 | 0.216185 | synonymous-codon | Hecw1 | Mm_Celera | 13:14377743 | CTGGGAGTGCCCTAT[C/T]GAATAGTAGGAACTG | 94253 |
rs46340796 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Hecw1 | Mm_Celera | 13:14321205 | TGGCTGTAATGAGTC[A/C]GAGTTCAGCCCAGCA | 94253 |
rs46351107 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Hecw1 | Mm_Celera | 13:14248636 | ATGAGTTTTTGTATA[A/G]TATTCAGCTTAAAAT | 94253 |
rs46363048 | snp | G/T | | | intron-variant | Hecw1 | GRCm38.p3 | 13:14398894 | GAGGCCCATTGGACT[G/T]GCAAACTTTATATGC | 94253 |
rs46367477 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Hecw1 | Mm_Celera | 13:14502906 | CTGTACCTCCGATAC[C/T]AAGCTGCAGGGTTTG | 94253 |
rs46368304 | snp | A/G | | | intron-variant | Hecw1 | Mm_Celera | 13:14339100 | ATATCTTATGATGCC[A/G]ATAGAGGATTTTAAG | 94253 |
rs46379576 | snp | A/T | 0.459184 | 0.136902 | intron-variant | Hecw1 | Mm_Celera | 13:14278201 | AAACCTCACTGGCCC[A/T]CTCCACAGTGCTGCT | 94253 |
rs46383159 | snp | G/T | | | intron-variant | Hecw1 | GRCm38.p3 | 13:14244657 | CTTTAGTGCTTTTTA[G/T]AAGGGTGAACAAAAT | 94253 |
rs46395748 | snp | A/G | 0.21875 | 0.248039 | intron-variant | Hecw1 | Mm_Celera | 13:14512265 | AAAAACTAGACTTTT[A/G]AAAATGATGTATCCA | 94253 |
rs46395863 | snp | C/T | | | intron-variant | Hecw1 | Mm_Celera | 13:14284236 | CCACCTCACACCAGT[C/T]AGAATGGCTAAGATC | 94253 |
rs46399078 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Hecw1 | Mm_Celera | 13:14379170 | TACTAACTTCAACTA[C/T]CACTGGGCTGTTGTC | 94253 |
rs46405821 | snp | G/T | 0.35503 | 0.226867 | intron-variant | Hecw1 | Mm_Celera | 13:14266346 | CTACAGTGCAATAAC[G/T]TTTATATTATACACA | 94253 |
rs46406442 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Hecw1 | Mm_Celera | 13:14343185 | TCTAAGAGCCTATAT[C/T]TGAATGGCAGAGACA | 94253 |
rs46413103 | snp | A/C | 0.35503 | 0.226867 | intron-variant | Hecw1 | Mm_Celera | 13:14250438 | CCTAAATTTCAGGGC[A/C]CTCCAATGACCCATG | 94253 |
rs46418890 | snp | A/T | 0.132653 | 0.220748 | intron-variant | Hecw1 | Mm_Celera | 13:14491531 | TCCAAATAAACGTTC[A/T]TTTACATATCTTTAA | 94253 |
rs46422871 | snp | A/T | 0.497778 | 0.0332592 | utr-variant-3-prime | Hecw1 | Mm_Celera | 13:14228593 | ATGTCATTTCTAAGA[A/T]AATTTCTTCCTTCTG | 94253 |
rs46443356 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Hecw1 | Mm_Celera | 13:14251280 | CATCATAGTGAGATG[C/T]CAAACTACAGCTCAT | 94253 |
rs46443561 | snp | A/C | 0.21875 | 0.248039 | intron-variant | Hecw1 | Mm_Celera | 13:14510692 | CCAGCCTCTCTTTAT[A/C]AGCAGCCTTTGCAGC | 94253 |
rs46453775 | snp | A/G | | | intron-variant | Hecw1 | Mm_Celera | 13:14232544 | TCACATCCTCTCTAT[A/G]TATTAATTTATTTCC | 94253 |
rs46464503 | snp | A/C | 0.244898 | 0.249948 | intron-variant | Hecw1 | Mm_Celera | 13:14503564 | ACAACTGGGTCTCAT[A/C]CAATATACACTCAAC | 94253 |
rs46469134 | snp | C/T | 0.32 | 0.24 | intron-variant, upstream-variant-2KB | Hecw1 | Mm_Celera | 13:14458504 | GATGGACGACACTGC[C/T]AAGTTTAGCCACTAG | 94253 |
rs46469286 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Hecw1 | Mm_Celera | 13:14270566 | AGGTTTCATTTTATT[G/T]TTCAGTTGGGCATGA | 94253 |
rs46473439 | snp | A/C | | | intron-variant | Hecw1 | GRCm38.p3 | 13:14241996 | GAAATGGAGGAAGTT[A/C]AAATAATTATCAGAT | 94253 |
rs46473688 | snp | C/T | | | intron-variant | Hecw1 | Mm_Celera | 13:14490055 | CAAACTCACCAAGTC[C/T]TAAGAGCCATGGCCA | 94253 |
rs46480615 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Hecw1 | Mm_Celera | 13:14424686 | CAGTTGCTTATTGTC[G/T]GAAGCAGTGTGTACA | 94253 |
rs46485334 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Hecw1 | Mm_Celera | 13:14246529 | CAGAGAGGTCTTCAC[C/T]CAAAAAGGGACTCAT | 94253 |
rs46486158 | snp | A/G | 0.473373 | 0.11227 | intron-variant | Hecw1 | Mm_Celera | 13:14421832 | CATCCTCATTTATGA[A/G]AAGGACACCAATGGG | 94253 |
rs46490132 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Hecw1 | Mm_Celera | 13:14406013 | ATAATAAAAGAAAAT[A/T]TCACATTAATCCTGT | 94253 |
rs46492604 | snp | A/T | 0.426035 | 0.177515 | intron-variant | Hecw1 | Mm_Celera | 13:14372069 | AGACTTCACCTATAG[A/T]GCCAAAGGAAAAGGG | 94253 |
rs46518354 | snp | A/G | 0.165289 | 0.235211 | intron-variant | Hecw1 | Mm_Celera | 13:14374384 | TAAGTTTGGATTGAG[A/G]AATTATGTTTGAAGT | 94253 |
rs46527044 | snp | A/C | | | intron-variant | Hecw1 | Mm_Celera | 13:14325585 | AACCTATAGTTCTTT[A/C]TATAGGGTGAGATCC | 94253 |
rs46530266 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Hecw1 | Mm_Celera | 13:14344344 | TCCCACCTAAAGAGA[C/T]ACATGATAATATCTG | 94253 |
rs46533529 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Hecw1 | Mm_Celera | 13:14425886 | GATGTTTGTAGACAT[G/T]TCCAGTGGGGCTGAA | 94253 |
rs46535040 | snp | A/C/G | 0.444444 | 0.157135 | intron-variant | Hecw1 | Mm_Celera | 13:14259703 | AAATGTGCAGAGAAC[A/C/G]TGTAGATTGAACCTA | 94253 |
rs46537413 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Hecw1 | Mm_Celera | 13:14501237 | GTACAAAGGGCTCCA[A/G]ACCAGGTAATACATT | 94253 |
rs46551975 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Hecw1 | Mm_Celera | 13:14361549 | TGTAGTAGAACAATG[C/T]ATAAAATGTACATGT | 94253 |
rs46552201 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Hecw1 | Mm_Celera | 13:14233819 | TTTAAATAGAGTAAA[G/T]AGTGTGGAAATCACT | 94253 |
rs46574661 | snp | A/G | 0.345679 | 0.230967 | intron-variant | Hecw1 | Mm_Celera | 13:14481463 | AAAAGAGATCTCTAT[A/G]TAAGATTGCTATGTT | 94253 |
rs46581351 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Hecw1 | Mm_Celera | 13:14425357 | TATCAGAATGATAAT[C/T]TTAAATAGATACTAG | 94253 |
rs46601218 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Hecw1 | Mm_Celera | 13:14347442 | TTGGATGTAGGTGCT[A/G]TCTTTTAATAGGAGA | 94253 |
rs46619593 | snp | A/T | 0.142012 | 0.225474 | intron-variant | Hecw1 | Mm_Celera | 13:14430473 | GGAAAGGAAGAAAAC[A/T]CTGCCCTATTTCTTA | 94253 |
rs46622808 | snp | A/C | 0.152778 | 0.230321 | intron-variant | Hecw1 | Mm_Celera | 13:14430034 | TGACTAAGAGGAATG[A/C]TTCCAGAGGCCCCAG | 94253 |
rs46622826 | snp | A/C | 0.497041 | 0.0383476 | intron-variant | Hecw1 | Mm_Celera | 13:14421982 | TAGGTAGGATTATAA[A/C]TGACAGGCCTAAATA | 94253 |
rs46622971 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Hecw1 | Mm_Celera | 13:14466519 | CTTTTGATCTTTCTC[C/T]CTGAGTCCCAATATG | 94253 |
rs46642158 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Hecw1 | Mm_Celera | 13:14472382 | AGTCCTTTTTTACAG[C/T]CACTCATGCAACAAT | 94253 |
rs46642989 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Hecw1 | Mm_Celera | 13:14389623 | CACTCTGTGAGCTTT[C/T]TGTAACTGAGATCTC | 94253 |
rs46648562 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Hecw1 | Mm_Celera | 13:14252654 | GTGAGCTCCATTAGT[C/T]ATCTATCCTTTGCTA | 94253 |
rs46649515 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Hecw1 | Mm_Celera | 13:14245890 | CCTTGCGAATAAACA[A/G]GAGGAGACATTTTTA | 94253 |
rs46664484 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Hecw1 | Mm_Celera | 13:14321109 | GGCTACCTAGTAGAC[A/G]TTCTTCCACAGTGAA | 94253 |
rs46665962 | snp | A/C/T | | | intron-variant | Hecw1 | GRCm38.p3 | 13:14307973 | TTACATACATATATG[A/C/T]ATATGTATGTATATA | 94253 |
rs46694611 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Hecw1 | Mm_Celera | 13:14340578 | CAGACCCTGGAGTTG[A/G]AGGCCTTAGAAAACA | 94253 |
rs46696717 | snp | A/T | 0.32 | 0.24 | intron-variant | Hecw1 | Mm_Celera | 13:14469622 | TACTATATCCATCCC[A/T]CTTTTCTGACCTCAT | 94253 |
rs46704466 | snp | G/T | 0.391111 | 0.206368 | intron-variant | Hecw1 | Mm_Celera | 13:14297837 | TTCAGAACCCTATCA[G/T]TCTAGCGAATCTTAT | 94253 |
rs46713011 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Hecw1 | Mm_Celera | 13:14460459 | TTGGACACTTCTAAA[C/T]GTGGCTGATATTAAT | 94253 |
rs46715399 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Hecw1 | Mm_Celera | 13:14467553 | CATCTTGCTTGTTTG[C/T]GTCCTTCCAGTTGTA | 94253 |
rs46728265 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Hecw1 | Mm_Celera | 13:14433397 | AAATGGCTATCTAGA[A/G]TGACAACCCTCTGAG | 94253 |
rs46743228 | snp | C/T | | | intron-variant | Hecw1 | Mm_Celera | 13:14386685 | GCGGACACCTCTCCT[C/T]TGATGGGGAAGGTGC | 94253 |
rs46758797 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Hecw1 | Mm_Celera | 13:14306303 | GAGAGGAGAGAGGAG[C/T]ACACCCTCCATGATG | 94253 |
rs46762568 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Hecw1 | Mm_Celera | 13:14252053 | CTACAACAGAGAATA[A/C]ACAAAACCAACCAGT | 94253 |
rs46763287 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Hecw1 | Mm_Celera | 13:14278181 | ACAGAGACGAAAGGT[A/G]GCATAAACCTCACTG | 94253 |
rs46772867 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Hecw1 | Mm_Celera | 13:14259911 | ACAGACTCCAAACCC[A/G]GCATTTTTGATGTGG | 94253 |
rs46779762 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Hecw1 | Mm_Celera | 13:14357409 | AAACCTATGTCATGA[A/G]AAATTGTGTGGGCTT | 94253 |
rs46786307 | snp | A/C | 0.497778 | 0.0332592 | intron-variant | Hecw1 | Mm_Celera | 13:14357900 | CAGGAAATGTCAGTG[A/C]TGGTAGTAATATGAG | 94253 |
rs46789787 | snp | A/G | 0.497041 | 0.0383476 | intron-variant | Hecw1 | Mm_Celera | 13:14413677 | TAAACAGTGTTTATG[A/G]CGTGCATAATAACTA | 94253 |
rs46795555 | snp | A/C | | | intron-variant | Hecw1 | Mm_Celera | 13:14452201 | GACCCCAGAAAATAA[A/C]ATAACCCCATTCAAA | 94253 |
rs46798863 | snp | G/T | 0.244898 | 0.249948 | intron-variant | Hecw1 | Mm_Celera | 13:14471959 | GAAAATTGCCTATGT[G/T]TTAATTGAGTCCATT | 94253 |
rs46806382 | snp | A/G | 0.124444 | 0.216185 | synonymous-codon | Hecw1 | Mm_Celera | 13:14247589 | TTCATTAACAGTGAA[A/G]GTGAGATCTAGAATG | 94253 |
rs46807018 | snp | G/T | 0.408163 | 0.193609 | intron-variant, utr-variant-5-prime | Hecw1 | Mm_Celera | 13:14457407 | TGCCCCTTAATCAGC[G/T]GAGTTAAGGCACATC | 94253 |
rs46810283 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Hecw1 | Mm_Celera | 13:14341489 | ATGTCAATTCTAATG[A/G]CACTGTGTACATATT | 94253 |
rs46816737 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Hecw1 | Mm_Celera | 13:14415319 | CCTATTTTAGTGCTA[A/G]TGTTAGTCACAATAA | 94253 |
rs46820467 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Hecw1 | Mm_Celera | 13:14491304 | AACCTGGTGAATCTT[G/T]GCTTCTCATTGAGTA | 94253 |
rs46823004 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Hecw1 | Mm_Celera | 13:14341787 | TAAATACACCCTGTG[A/T]AGAGCTAGGCACTCA | 94253 |
rs46829362 | snp | A/G | 0.32 | 0.24 | intron-variant | Hecw1 | Mm_Celera | 13:14466458 | ATTCTTGAGACACAA[A/G]GTTACTCTGTTCTGT | 94253 |
rs46842072 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Hecw1 | Mm_Celera | 13:14434288 | GCAGGGTGAGTGATG[A/G]ATCTCAAATATTGAG | 94253 |
rs46850182 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Hecw1 | Mm_Celera | 13:14380212 | CTTTGTTTACATGGA[C/T]CAATCCAAAATTGGG | 94253 |
rs46857527 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Hecw1 | Mm_Celera | 13:14325049 | AGGTAGAAATAGAGG[A/T]CCTTTACCTACTATA | 94253 |
rs46858901 | snp | C/T | 0.297521 | 0.245442 | intron-variant | Hecw1 | Mm_Celera | 13:14304170 | TTGTTTTATTAAAAA[C/T]GTTACCTGTAATTAA | 94253 |
rs46875828 | snp | C/G | 0.35503 | 0.226867 | intron-variant | Hecw1 | Mm_Celera | 13:14346535 | GATTAATGTTCTGGA[C/G]ATAAGATGCAAAGTA | 94253 |
rs46878113 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Hecw1 | Mm_Celera | 13:14293225 | CATATTTGTTTTTGA[C/T]CCTCCAAAGACCAAG | 94253 |
rs46889609 | snp | C/G | 0.426035 | 0.177515 | intron-variant | Hecw1 | Mm_Celera | 13:14414151 | CCCCTCCCAGCATGT[C/G]CTCATAGTGAAGAGT | 94253 |
rs46894654 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Hecw1 | Mm_Celera | 13:14273037 | ACAGCTGCACTGGAA[G/T]TATGGGTGATGTCTT | 94253 |
rs46910951 | snp | C/T | 0.459184 | 0.136902 | intron-variant | Hecw1 | Mm_Celera | 13:14467821 | GGCTGAGCTCTGATC[C/T]TATGTCTCCTTGAGT | 94253 |
rs46913227 | snp | A/G | 0.375 | 0.216506 | intron-variant | Hecw1 | Mm_Celera | 13:14252183 | CATAAATGTGCTCAT[A/G]TTTATTTCTCTTTCC | 94253 |
rs46917348 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Hecw1 | Mm_Celera | 13:14282583 | TTGCTCAGCAGAAAG[C/T]AGTTATAAGCAGGAA | 94253 |
rs46919203 | snp | C/T | | | intron-variant | Hecw1 | Mm_Celera | 13:14239719 | TTGGCATCATCAGAA[C/T]CCAGTTCTCCCAGCA | 94253 |
rs46937079 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Hecw1 | Mm_Celera | 13:14388957 | GTTGTCATTCATCAC[C/T]ATGTTTCTTGAAGTG | 94253 |
rs46937994 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Hecw1 | Mm_Celera | 13:14492518 | TATGAGATAAATGTT[C/T]TTCTTCCTGCATGCA | 94253 |
rs46948509 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Hecw1 | Mm_Celera | 13:14264618 | GTAGTTGAATTGCAC[A/G]CGTAGGTAATTAATG | 94253 |
rs46949642 | snp | G/T | | | intron-variant | Hecw1 | Mm_Celera | 13:14414117 | TCAAACTTCCTGAAC[G/T]CCATTTCAGGTAAAC | 94253 |
rs46969408 | snp | C/T | 0.459184 | 0.136902 | intron-variant | Hecw1 | Mm_Celera | 13:14444858 | ATTCTCTATCCTTAG[C/T]TTTGTGTAAGCCATA | 94253 |
rs46981483 | snp | A/G | 0.32 | 0.24 | intron-variant | Hecw1 | Mm_Celera | 13:14376780 | TAATTACACTATGTA[A/G]AGCTGTCAAGAGAAT | 94253 |
rs46992033 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Hecw1 | Mm_Celera | 13:14491211 | TATTTTTTAACTTTC[A/G]GTATGCCTCAAAGTG | 94253 |
rs46995406 | snp | G/T | 0.124444 | 0.216185 | intron-variant, upstream-variant-2KB | Hecw1 | Mm_Celera | 13:14459265 | GTCATATTGTTTCTC[G/T]CTGAGAGCTCCTGAG | 94253 |
rs46998761 | snp | C/G | 0.391111 | 0.206368 | intron-variant | Hecw1 | Mm_Celera | 13:14233133 | CTGATTCTCCCTTAT[C/G]CTGAAATTAGTTATC | 94253 |
rs47002109 | snp | A/T | | | intron-variant | Hecw1 | Mm_Celera | 13:14477338 | GAAGAAAGAAATTAA[A/T]GAAGATCTCAGAAGA | 94253 |
rs47003627 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Hecw1 | Mm_Celera | 13:14482725 | GGCATGGTTGAGCTC[C/T]GAGGCTTCAAATGGT | 94253 |
rs47009442 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Hecw1 | Mm_Celera | 13:14357017 | TGAGAAATTGCAGAT[A/G]TGTACACGTATATAA | 94253 |
rs47019840 | snp | C/G | 0.408163 | 0.193609 | intron-variant | Hecw1 | Mm_Celera | 13:14481401 | GTTGGTTCATGATGA[C/G]TGTCTCTAGATAAAA | 94253 |
rs47020390 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Hecw1 | Mm_Celera | 13:14248810 | GAAATGCAGGAACCT[A/G]AAATATAAAGCACAA | 94253 |
rs47025073 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Hecw1 | Mm_Celera | 13:14434145 | AAGGACCACCACAGA[A/G]CAATTGATTCCACAT | 94253 |
rs47027171 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Hecw1 | Mm_Celera | 13:14358658 | CCTGTGGCCAGATCT[C/T]TTTCCAAACACCATT | 94253 |
rs47027947 | snp | A/C | | | intron-variant | Hecw1 | Mm_Celera | 13:14307901 | CTTCTCTCAAACTCT[A/C]CCATATACCTCATCT | 94253 |
rs47031181 | snp | C/T | 0.132653 | 0.220748 | intron-variant, utr-variant-5-prime | Hecw1 | Mm_Celera | 13:14455002 | TCACATCCAGGGCTC[C/T]GGGTTTTCTTGAAGG | 94253 |
rs47043359 | snp | A/G | 0.32 | 0.24 | intron-variant | Hecw1 | Mm_Celera | 13:14358805 | ATCTACTTGATTAAT[A/G]GTGAGATTAAACATT | 94253 |
rs47044847 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Hecw1 | Mm_Celera | 13:14324857 | TTTTCATACTCAGCC[C/T]TCAGCAATCTGGTGA | 94253 |
rs47054979 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Hecw1 | Mm_Celera | 13:14433610 | GTCTATAGAGGCCAT[A/G]AAGATTAGAGGAGTC | 94253 |
rs47067821 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Hecw1 | Mm_Celera | 13:14297687 | TCCTAGTGTCAGTTA[C/T]ACTTGGGCTCTTTCA | 94253 |
rs47070840 | snp | A/C | 0.473373 | 0.11227 | intron-variant | Hecw1 | Mm_Celera | 13:14423528 | AGGTCACCTTCTAGG[A/C]CAGCAGGGAGGTGAG | 94253 |
rs47071696 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Hecw1 | Mm_Celera | 13:14359336 | AGAAAATGATTGCAA[C/T]GCCTTTGAACAAATG | 94253 |
rs47078771 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Hecw1 | Mm_Celera | 13:14261480 | ACATTCTGGCAAGTC[A/G]TTGGCTAAACATGTC | 94253 |
rs47083603 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Hecw1 | Mm_Celera | 13:14387062 | GATGAGAACAAAGAC[A/G]TAGATGGAAACATTG | 94253 |
rs47089509 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Hecw1 | Mm_Celera | 13:14232835 | TGGAATTCTCAGAGG[C/T]GATTCAAGTTCCCAA | 94253 |
rs47103325 | snp | A/T | | | intron-variant | Hecw1 | Mm_Celera | 13:14307956 | TTTATCATTAGTTGT[A/T]GTTACATACATATAT | 94253 |
rs47114114 | snp | A/G | 0.32 | 0.24 | intron-variant | Hecw1 | Mm_Celera | 13:14233401 | TATAGGAAAACCTGA[A/G]AACTACTTTCAACTG | 94253 |
rs47114920 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Hecw1 | Mm_Celera | 13:14427279 | GCCTGAAAATTTCAT[C/T]AGATCTCCTGAGACT | 94253 |
rs47120669 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Hecw1 | Mm_Celera | 13:14433051 | TTTCCACAGCACTAT[A/G]CAATGTAGGAATTTA | 94253 |
rs47125923 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Hecw1 | Mm_Celera | 13:14388662 | CAAAAAGATTCTATT[C/T]CAAAGTGAGAGAAAG | 94253 |
rs47131422 | snp | C/G | 0.124444 | 0.216185 | intron-variant, upstream-variant-2KB | Hecw1 | Mm_Celera | 13:14459308 | CTTCCACATTGCCCT[C/G]AGCATTACTGTCTTA | 94253 |
rs47137301 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Hecw1 | Mm_Celera | 13:14377239 | TTGTAGAGTGATATC[A/G]TGAAAGCTAGCTTCT | 94253 |
rs47138253 | snp | A/G | | | intron-variant | Hecw1 | Mm_Celera | 13:14493561 | ATGATTCAAGTCTTG[A/G]CTTCACAAACAAATG | 94253 |
rs47154774 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Hecw1 | Mm_Celera | 13:14264640 | TAATTAATGAAGTCA[C/T]AGAAAGCACATGAAA | 94253 |
rs47155018 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Hecw1 | Mm_Celera | 13:14361598 | TATGATCAGTAGTGC[G/T]GACTTAGACAGCAGT | 94253 |
rs47158121 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Hecw1 | Mm_Celera | 13:14460849 | CTGTGTAAATTGGAT[A/G]TGGTGGTATGTGCCT | 94253 |
rs47164235 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Hecw1 | Mm_Celera | 13:14252019 | GGAACACAGGAGAAG[A/G]CTGACAAAGGACAAG | 94253 |
rs47164409 | snp | A/C/G | 0.297521 | 0.245442 | intron-variant, upstream-variant-2KB | Hecw1 | Mm_Celera | 13:14458021 | ACACAGTGAGGGGCC[A/C/G]TGTATGTCCAGTATC | 94253 |
rs47168846 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Hecw1 | Mm_Celera | 13:14364865 | CTGCACTCAGGAAAG[C/T]CCACTCACTAGTCAT | 94253 |
rs47171398 | snp | A/C | 0.375 | 0.216506 | intron-variant, utr-variant-5-prime | Hecw1 | Mm_Celera | 13:14457020 | CAAAGGGAAAACACC[A/C]CAGATAGTCTAGAAC | 94253 |
rs47180474 | snp | C/T | 0.375 | 0.216506 | intron-variant | Hecw1 | Mm_Celera | 13:14372222 | AACAGAGCATTTTTT[C/T]CACTCAACACGTGGC | 94253 |
rs47182882 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Hecw1 | Mm_Celera | 13:14247028 | GAAGATGCCCTGGCT[A/G]GGCTATTAAAAAAGA | 94253 |
rs47183482 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Hecw1 | Mm_Celera | 13:14277158 | CTGCCTGCCATATTA[C/T]CCAAGTATTATCTTT | 94253 |
rs47183634 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Hecw1 | Mm_Celera | 13:14388472 | TTACTCAAGGAAGCT[C/T]CCAGGACATTTTTAC | 94253 |
rs47192007 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Hecw1 | Mm_Celera | 13:14305127 | CCAAGAAACTCAGTG[A/G]ACCACACATACAGAT | 94253 |
rs47192240 | snp | C/T | | | intron-variant | Hecw1 | Mm_Celera | 13:14289193 | CCTCCAAGAGGAACT[C/T]TCAATTCTGAATATC | 94253 |
rs47196458 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Hecw1 | Mm_Celera | 13:14271994 | CAAGAAGGTCTCAGG[C/T]CCAACCTCTTACCTC | 94253 |
rs47210945 | snp | C/T | 0.231111 | 0.249285 | intron-variant, upstream-variant-2KB | Hecw1 | Mm_Celera | 13:14458172 | CAACTCCGAGTTAGC[C/T]ATTCACGCAGAACAG | 94253 |
rs47211089 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | Hecw1 | Mm_Celera | 13:14388074 | TGTTTTGTAATCAAA[A/G]CATTGTAGGAGTTTC | 94253 |
rs47213550 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Hecw1 | Mm_Celera | 13:14260416 | GTACAGATTGGAATG[A/G]TTAATATATGTATAT | 94253 |
rs47213648 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Hecw1 | Mm_Celera | 13:14491326 | CATTGAGTAACTAGC[A/G]TGCTCACTGATCTAT | 94253 |
rs47224004 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Hecw1 | Mm_Celera | 13:14344552 | TGGGTTTTATGCAAT[A/G]GCGTTCTTCTGAAGT | 94253 |
rs47227333 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Hecw1 | Mm_Celera | 13:14352941 | TCTGGTGGCCTTTTC[C/T]CAGCTGCATGGATAT | 94253 |
rs47235852 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Hecw1 | Mm_Celera | 13:14426751 | ACATTTGATTCCTAA[A/T]ACAAGAACTCTGATG | 94253 |
rs47237715 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Hecw1 | Mm_Celera | 13:14351728 | AGGATAATATGAATG[C/T]AGAAACACACAAAAC | 94253 |
rs47237992 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Hecw1 | Mm_Celera | 13:14490880 | AATGGCATAAGATAG[A/G]CATAGCCATGTACTG | 94253 |
rs47241467 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Hecw1 | Mm_Celera | 13:14298920 | TCCCCATTCTCTTTA[A/C]ACTTCCAAGACTCAA | 94253 |
rs47246112 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Hecw1 | Mm_Celera | 13:14236479 | ACAGTAGCAGCAATT[C/T]GAGATAATGGTGTGA | 94253 |
rs47246353 | snp | G/T | 0.231111 | 0.249285 | intron-variant, upstream-variant-2KB | Hecw1 | Mm_Celera | 13:14457946 | GATCTGGGGACTCTC[G/T]TATACTCTGTATTAT | 94253 |
rs47247256 | snp | C/T | | | intron-variant | Hecw1 | Mm_Celera | 13:14253738 | CTTCTCCCATTGATG[C/T]CCAACAAGACCATCA | 94253 |
rs47251114 | snp | A/C | | | intron-variant | Hecw1 | Mm_Celera | 13:14477425 | CTTGCCAAAAGCAAT[A/C]TACAGATTCAATGCA | 94253 |
rs47253682 | snp | A/T | | | intron-variant | Hecw1 | Mm_Celera | 13:14318544 | CATTCATTCATTTAC[A/T]CATGTATAGAATGAT | 94253 |
rs47266852 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Hecw1 | Mm_Celera | 13:14234548 | GAGGAAGAGACAGAT[A/G]TGTTAACTGAACTGG | 94253 |
rs47267615 | snp | C/G | 0.277778 | 0.248452 | intron-variant, upstream-variant-2KB | Hecw1 | Mm_Celera | 13:14457981 | ACAAGCTGTTCAGCA[C/G]TCTTGGGCATTTAGA | 94253 |
rs47272773 | snp | A/C | 0.473373 | 0.11227 | intron-variant | Hecw1 | Mm_Celera | 13:14498464 | AGAGTGGAGAGTCAC[A/C]CTGGAGTCAGCTGGA | 94253 |
rs47291144 | snp | C/G | 0.391111 | 0.206368 | downstream-variant-500B | Hecw1 | Mm_Celera | 13:14226124 | GTTTTCATAGAAATT[C/G]TTAACAGATAGGATT | 94253 |
rs47301389 | snp | A/T | 0.32 | 0.24 | intron-variant | Hecw1 | Mm_Celera | 13:14472773 | GTACAGATTGCATGT[A/T]ATGGAGTTCAAAGAA | 94253 |
rs47304896 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Hecw1 | Mm_Celera | 13:14454810 | CTTCCACAAGTCCCA[C/T]TGCCAATGCAGTCAT | 94253 |
rs47312027 | snp | A/G | 0.152778 | 0.230321 | intron-variant, utr-variant-5-prime | Hecw1 | Mm_Celera | 13:14455811 | TCAGGCTAGTATACC[A/G]CTGTAATTCAGCTGA | 94253 |
rs47320232 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Hecw1 | Mm_Celera | 13:14259979 | TTTCTTGGGAGGTCC[A/G]ACCAGCAACTGACTA | 94253 |
rs47327403 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Hecw1 | Mm_Celera | 13:14231887 | GATTCAGGATAGTGC[C/T]GCTTCTTTGGGAGAT | 94253 |
rs47329215 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Hecw1 | Mm_Celera | 13:14463697 | GTTGCATTTAGAAGC[A/G]TGGCAAAAATGTAAG | 94253 |
rs47348412 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Hecw1 | Mm_Celera | 13:14249929 | ATTTGTTTCCTAGAA[A/C]GTTTTCTGGTGAACT | 94253 |
rs47367252 | snp | C/T | 0.32 | 0.24 | synonymous-codon | Hecw1 | GRCm38.p3 | 13:14245741 | TACCTCATAGAAACC[C/T]CTGAGCAATGCCTCC | 94253 |
rs47373656 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Hecw1 | Mm_Celera | 13:14465905 | GAACTTCCATGTACT[A/G]TCCCTGAGAAAATTA | 94253 |
rs47375073 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Hecw1 | Mm_Celera | 13:14306615 | GCCATTCAAGCTTAA[C/T]GTGCTCTCTGTCACT | 94253 |
rs47380519 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Hecw1 | Mm_Celera | 13:14479430 | ATTACCCCTATTTTA[C/G]TTTCTTTCTAGTAAC | 94253 |
rs47386439 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Hecw1 | Mm_Celera | 13:14235373 | TTCAGGTGCCTGGCT[A/G]AAGGAGGCTGAGTTG | 94253 |
rs47387616 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Hecw1 | Mm_Celera | 13:14479059 | GGTCCTGATATACTT[C/T]GATATAACATTCTAA | 94253 |
rs47402882 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Hecw1 | Mm_Celera | 13:14352388 | CCATGAATATGAGAA[A/G]ATCATAAAACCTGGC | 94253 |
rs47407449 | snp | A/G | 0.260355 | 0.249785 | intron-variant, utr-variant-5-prime | Hecw1 | Mm_Celera | 13:14455078 | AAGCATTAGAGAAAA[A/G]AAGCCACAAGCTGCC | 94253 |
rs47416561 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Hecw1 | Mm_Celera | 13:14234002 | CAGCATTTTTACAGT[A/C]AAGACCTTGCTGTCA | 94253 |
rs47422623 | snp | A/G | 0.197531 | 0.244432 | intron-variant | Hecw1 | Mm_Celera | 13:14439133 | GCTGCTTCCAGGACA[A/G]CCTCTTCTGTGCTTA | 94253 |
rs47431856 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Hecw1 | Mm_Celera | 13:14364835 | GGGAAAAAAAACCAT[C/T]TAGGCCTGCTGTTTC | 94253 |
rs47444925 | snp | C/G | | | intron-variant | Hecw1 | Mm_Celera | 13:14251452 | TGCCTGTAATCCAAG[C/G]ACTGGGGAGACCGAG | 94253 |
rs47447381 | snp | A/G | 0.5 | 0 | intron-variant | Hecw1 | Mm_Celera | 13:14425052 | TGCCTTGAAAAAATA[A/G]TCACGCCATGTGCAC | 94253 |
rs47473469 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Hecw1 | Mm_Celera | 13:14279791 | TATATTAAAAAACCA[A/G]CACCTGCATGTAGAT | 94253 |
rs47491482 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Hecw1 | Mm_Celera | 13:14259898 | ATTCATCATGTCCAC[A/G]GACTCCAAACCCGGC | 94253 |
rs47504749 | snp | C/T | 0.396694 | 0.202437 | intron-variant | Hecw1 | Mm_Celera | 13:14461225 | TAATCAGATAATAGC[C/T]CTGTCCTCAGAGGCA | 94253 |
rs47504784 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Hecw1 | Mm_Celera | 13:14253297 | GGCTCTGGTCAACAC[A/G]GTGACTTCTCTGGGG | 94253 |
rs47509429 | snp | G/T | 0.18 | 0.24 | intron-variant | Hecw1 | Mm_Celera | 13:14369419 | GGGACATGTACTGAC[G/T]CTCAATTTAAATTTA | 94253 |
rs47511081 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Hecw1 | Mm_Celera | 13:14425119 | AAGTCTCTTCTACAT[C/T]GCTCTGGTTTTAGAC | 94253 |
rs47513093 | snp | A/T | 0.152778 | 0.230321 | intron-variant | Hecw1 | Mm_Celera | 13:14235378 | GTGCCTGGCTGAAGG[A/T]GGCTGAGTTGGTATT | 94253 |
rs47519692 | snp | A/G | 0.391111 | 0.206368 | synonymous-codon | Hecw1 | GRCm38.p3 | 13:14230738 | ATGGTGGGAGATCCA[A/G]TCGGTTGAAGCACGT | 94253 |
rs47531386 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Hecw1 | Mm_Celera | 13:14425310 | CCTTGACTTTTGCTA[C/G]TAGCTCTGGTTCTGT | 94253 |
rs47533454 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Hecw1 | Mm_Celera | 13:14249896 | AGGCCCTTACTTATA[A/T]CAATCATTGTTGAAT | 94253 |
rs47537965 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Hecw1 | Mm_Celera | 13:14345220 | GGTTAATAAACCTTT[A/G]CCTAGACTTTCCCAG | 94253 |
rs47543648 | snp | C/T | 0.32 | 0.24 | intron-variant | Hecw1 | Mm_Celera | 13:14236462 | CCTAGGCATTGTAAA[C/T]CACAGTAGCAGCAAT | 94253 |
rs47544250 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Hecw1 | Mm_Celera | 13:14234013 | CAGTAAAGACCTTGC[C/T]GTCACAATCGCCTAA | 94253 |
rs47547923 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Hecw1 | Mm_Celera | 13:14308892 | TGCTATAAACTAGGA[A/G]TTACAGGAAGTTCTA | 94253 |
rs47549274 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Hecw1 | Mm_Celera | 13:14264758 | ATGTCCAATTGGTTA[A/G]GATTTTAATTTATAT | 94253 |
rs47554185 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Hecw1 | Mm_Celera | 13:14291897 | AATGTCAAAGAGTAG[C/T]ATGACAGAACTTGAA | 94253 |
rs47554290 | snp | A/C | 0.197531 | 0.244432 | intron-variant, upstream-variant-2KB | Hecw1 | Mm_Celera | 13:14459514 | CCAGGGCAATTTATC[A/C]AAAAACAGAGTTTAT | 94253 |
rs47563692 | snp | A/T | 0.277778 | 0.248452 | intron-variant | Hecw1 | Mm_Celera | 13:14490938 | TTATTTTAGTTTATG[A/T]ATGTTTCATATGAAC | 94253 |
rs47578548 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Hecw1 | Mm_Celera | 13:14496299 | AAAACTTTCACATAC[A/G]CTATTCCTGGAAGCC | 94253 |
rs47590464 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Hecw1 | Mm_Celera | 13:14469210 | TTTGATGAGCTCACA[C/T]TTGATTGTTCATTTT | 94253 |
rs47591370 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Hecw1 | Mm_Celera | 13:14340355 | TTGTGGGATGCTCAG[A/G]TCAAGGCTGGTCTTT | 94253 |
rs47596646 | snp | G/T | 0.336735 | 0.234472 | synonymous-codon | Hecw1 | Mm_Celera | 13:14316447 | CTCACTCCCAGTGCT[G/T]GGGTGAGCTTCGCCA | 94253 |
rs47601998 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Hecw1 | Mm_Celera | 13:14352088 | CATTATGAAATGGGC[A/C]AAATGTACTCTTGTC | 94253 |
rs47605607 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Hecw1 | Mm_Celera | 13:14353025 | ATGACTAGCTGCTGA[C/T]GGTGTCTTAGAAGAC | 94253 |
rs47606233 | snp | A/G | 0.35503 | 0.226867 | intron-variant | Hecw1 | Mm_Celera | 13:14364369 | GGTTAGATAATAACC[A/G]CAGAGGCTTCCAGCT | 94253 |
rs47609213 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Hecw1 | Mm_Celera | 13:14321422 | GACAGGTTGGACTTG[A/G]TCTTGGAGTAAGGCA | 94253 |
rs47621242 | snp | C/T | 0.46281 | 0.131194 | intron-variant | Hecw1 | Mm_Celera | 13:14378403 | TATTTCAGTCATTCC[C/T]GATGCATTTAATCCT | 94253 |
rs47641174 | snp | A/G | 0.391111 | 0.206368 | intron-variant, utr-variant-5-prime | Hecw1 | Mm_Celera | 13:14455140 | GCCAAGAATCTTGGA[A/G]CTCTCCTCAAAGATG | 94253 |
rs47645713 | snp | A/G | 0.426035 | 0.177515 | intron-variant, utr-variant-5-prime | Hecw1 | Mm_Celera | 13:14455853 | ATCTGCCTGTCCATC[A/G]GGTCCTCTGACAAGA | 94253 |
rs47646275 | snp | C/T | 0.32 | 0.24 | intron-variant, utr-variant-5-prime | Hecw1 | Mm_Celera | 13:14457149 | CCAGAGAATATTGAA[C/T]CTGGGAGTAAGCCGA | 94253 |
rs47647314 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Hecw1 | Mm_Celera | 13:14482568 | ACCCCTTGTCATCTT[C/T]GCTCAACACATACAA | 94253 |
rs47647865 | snp | C/T | | | intron-variant | Hecw1 | Mm_Celera | 13:14433884 | GTTTAGTAACAATGA[C/T]GTGGAAAAAGGAGGT | 94253 |
rs47653019 | snp | A/T | 0.497778 | 0.0332592 | intron-variant | Hecw1 | Mm_Celera | 13:14425259 | ACAAGAACAGCTTCA[A/T]AGAGAGCATGGTATG | 94253 |
rs47663466 | snp | C/T | 0.32 | 0.24 | intron-variant | Hecw1 | Mm_Celera | 13:14473589 | GCACCCAGGAACAGA[C/T]CCTGTGCTCCAGTCC | 94253 |
rs47673067 | snp | A/G | 0.473373 | 0.11227 | intron-variant | Hecw1 | Mm_Celera | 13:14414465 | TACAAGCAGAATTCC[A/G]AACACAGATCAAGAT | 94253 |
rs47678213 | snp | G/T | 0.486111 | 0.0821678 | intron-variant | Hecw1 | Mm_Celera | 13:14324842 | AGAAAATTTAGAAGA[G/T]TTTCATACTCAGCCT | 94253 |
rs47690267 | snp | C/T | | | intron-variant | Hecw1 | Mm_Celera | 13:14242731 | AGCCTTGTCTAGTCC[C/T]TGATTTTAGTAGGAT | 94253 |
rs47692782 | snp | C/T | 0.32 | 0.24 | intron-variant | Hecw1 | Mm_Celera | 13:14482507 | CTCAGTCCAGAGAAC[C/T]TGGCACCCTCTTGGT | 94253 |
rs47698345 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Hecw1 | Mm_Celera | 13:14364309 | AGTATAAATCCATGA[C/G]TCTTCAGAAGGATGA | 94253 |
rs47708704 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Hecw1 | Mm_Celera | 13:14352823 | AGACAATATAAGAAA[C/T]ACATTATTACACTGT | 94253 |
rs47717282 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Hecw1 | Mm_Celera | 13:14270356 | AAATGCTTGGAGCAG[C/T]CATTGGGGCACAATG | 94253 |
rs47717849 | snp | A/C | 0.21875 | 0.248039 | intron-variant | Hecw1 | Mm_Celera | 13:14514816 | CACAGACACACATGA[A/C]ACAATTATAATCTAG | 94253 |
rs47726832 | snp | C/G | 0.244898 | 0.249948 | intron-variant | Hecw1 | Mm_Celera | 13:14473273 | TAATCCAACCTTACT[C/G]CATTCATTATGGATC | 94253 |
rs47732282 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | Hecw1 | Mm_Celera | 13:14364991 | TTGATTCAGAGCTAG[A/G]ATACAGTAATAGTGT | 94253 |
rs47750139 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Hecw1 | Mm_Celera | 13:14482968 | TTATAGACTAATAAA[G/T]AACAGCAGCCATAAA | 94253 |
rs47750665 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Hecw1 | Mm_Celera | 13:14272845 | TCACATATACCCTTC[A/C]CTTGGTTTACCCCAG | 94253 |
rs47762406 | snp | A/C | 0.391111 | 0.206368 | intron-variant | Hecw1 | Mm_Celera | 13:14271869 | ATAAGGATGCACAGT[A/C]AGTGCTGCCAATCAA | 94253 |
rs47765992 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Hecw1 | Mm_Celera | 13:14298542 | AGATCCAAGCAGCAT[G/T]AACTGTTTTCTCAGC | 94253 |
rs47770671 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Hecw1 | Mm_Celera | 13:14250677 | ATTAATGTTCTGGTA[A/G]TATTTTCAGGATGAA | 94253 |
rs47774998 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Hecw1 | Mm_Celera | 13:14233375 | CTTTTTGTCTTGATG[A/G]CTAGAACTAGTATAG | 94253 |
rs47775885 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Hecw1 | Mm_Celera | 13:14472565 | CCACTCCCTTATTTC[A/G]CACAAGCAATTATTT | 94253 |
rs47785776 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Hecw1 | Mm_Celera | 13:14353837 | ACTATGAGTTCTCAA[C/T]TACAAGGCTTACATT | 94253 |
rs47788353 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Hecw1 | Mm_Celera | 13:14480386 | CACACAAACCACACA[A/G]ACTACATGTAAAACA | 94253 |
rs47792814 | snp | A/G | 0.124444 | 0.216185 | utr-variant-3-prime | Hecw1 | Mm_Celera | 13:14228719 | ATTCTCCTTTTCAAT[A/G]TATGGCAAGTCAGTG | 94253 |
rs47803918 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Hecw1 | Mm_Celera | 13:14415163 | TTAAACTCTTTGCCA[C/T]GACTTACTAATGAGA | 94253 |
rs47813775 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Hecw1 | Mm_Celera | 13:14479037 | CTACAGCCCATCGAG[A/G]GAACATGGTCCTGAT | 94253 |
rs47820879 | snp | C/G | 0.473373 | 0.11227 | intron-variant | Hecw1 | Mm_Celera | 13:14422362 | AACACATATAGATTA[C/G]TGAAAAAAGTTTTAT | 94253 |
rs47822084 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Hecw1 | Mm_Celera | 13:14497809 | AGGCCTCAGTGGGAA[A/G]TAATGAGTATGGTCT | 94253 |
rs47834445 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Hecw1 | Mm_Celera | 13:14341657 | AAGTTGTTTTGCAAG[G/T]TCAGGACATAAGAAA | 94253 |
rs47838200 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Hecw1 | Mm_Celera | 13:14387786 | ACAGAAATATAAGAA[A/G]GAGACAATAAGTTGT | 94253 |
rs47843916 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Hecw1 | Mm_Celera | 13:14272107 | TAGAATAAAGTTGAA[A/G]AGAAAGTAAGAATTG | 94253 |
rs47845637 | snp | C/T | 0.459184 | 0.136902 | intron-variant, utr-variant-5-prime | Hecw1 | Mm_Celera | 13:14456961 | TTAGAAGCTCATCTT[C/T]ACACAGCAGTAAAGC | 94253 |
rs47854374 | snp | C/T | 0.5 | 0 | intron-variant | Hecw1 | Mm_Celera | 13:14499582 | ATGGCAGAATTAGTC[C/T]CCTATGAAGAAACTA | 94253 |
rs47855117 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Hecw1 | Mm_Celera | 13:14364860 | TGTTTCTGCACTCAG[A/G]AAAGTCCACTCACTA | 94253 |
rs47858928 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Hecw1 | Mm_Celera | 13:14249687 | GGCCACATGCTGGGA[A/G]ACAGAAGCTTGAATA | 94253 |
rs47865516 | snp | A/T | 0.345679 | 0.230967 | intron-variant | Hecw1 | Mm_Celera | 13:14511940 | ATAGTTTGGATAAGG[A/T]GATTCCACCAACTCT | 94253 |
rs47867688 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Hecw1 | Mm_Celera | 13:14344482 | GACACACTTGCTATG[G/T]AGAAGTAATTTGATA | 94253 |
rs47868879 | snp | A/G | 0.444444 | 0.157135 | utr-variant-3-prime | Hecw1 | GRCm38.p3 | 13:14227000 | TCAGACATGTGGCTT[A/G]ATACATGAACTATTG | 94253 |
rs47876797 | snp | C/T | 0.375 | 0.216506 | intron-variant | Hecw1 | Mm_Celera | 13:14470102 | TGAGCACATTCGCAG[C/T]ACACTCTATTTGATC | 94253 |
rs47881233 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Hecw1 | Mm_Celera | 13:14360749 | TATCTTCCTCTTATT[A/T]AACCTAAATTTGTAT | 94253 |
rs47883812 | snp | C/T | 0.473373 | 0.11227 | intron-variant | Hecw1 | Mm_Celera | 13:14415251 | ACCGGGCAATAATCC[C/T]ATGAAAAGCACTGAA | 94253 |
rs47886126 | snp | A/G | 0.5 | 0 | intron-variant | Hecw1 | Mm_Celera | 13:14318373 | TTGATATGGAGAGTG[A/G]AATATAGAATGTTTC | 94253 |
rs47886932 | snp | C/T | 0.489796 | 0.070696 | intron-variant | Hecw1 | Mm_Celera | 13:14310898 | TTCAAACAGAGAGGT[C/T]CCAGAATTCATAAGT | 94253 |
rs47897768 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Hecw1 | Mm_Celera | 13:14472835 | AGATACATATGACAC[A/G]TAGAATTTAGTGATA | 94253 |
rs47915063 | snp | C/G | | | intron-variant | Hecw1 | GRCm38.p3 | 13:14240915 | ACTCAGAATTTTGCT[C/G]CATACAGGAAACATA | 94253 |
rs47917872 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Hecw1 | Mm_Celera | 13:14233990 | ACTTTGCATTTCCAG[C/G]ATTTTTACAGTAAAG | 94253 |
rs47922209 | snp | C/T | | | intron-variant | Hecw1 | Mm_Celera | 13:14433641 | AGGTTCCATCTAGGC[C/T]GATAAGGGGAGGCTC | 94253 |
rs47923164 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Hecw1 | Mm_Celera | 13:14285372 | AGACAAATCAAGGCA[A/G]CTAATGGGCACCCCA | 94253 |
rs47923347 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Hecw1 | Mm_Celera | 13:14361805 | AAATACAACTGGAGG[C/T]TCTTCTTTGTAAGTA | 94253 |
rs47928380 | snp | A/T | 0.197531 | 0.244432 | intron-variant, utr-variant-5-prime | Hecw1 | Mm_Celera | 13:14455821 | ATACCACTGTAATTC[A/T]GCTGATTGGAGTTAC | 94253 |
rs47930668 | snp | A/C/T | 0.124444 | 0.216185 | intron-variant | Hecw1 | Mm_Celera | 13:14461773 | ACCATATTGTTCCTG[A/C/T]TATCAAGACTCAAAG | 94253 |
rs47937582 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Hecw1 | Mm_Celera | 13:14387884 | ATTGTAATTTCCTGT[A/T]TTACTAAAATGTAGT | 94253 |
rs47946495 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Hecw1 | Mm_Celera | 13:14233698 | TCAGATCAGAATAAA[A/G]AGGACCATGTAAAAC | 94253 |
rs47956334 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Hecw1 | Mm_Celera | 13:14235246 | TATCTGTAGAGGCCC[A/G]AGCCAGGGAATTGCT | 94253 |
rs47956857 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Hecw1 | Mm_Celera | 13:14467603 | AAGACGCACCAGTTT[C/T]CCTACATCCAGGAGT | 94253 |
rs47957998 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Hecw1 | Mm_Celera | 13:14233734 | ACTGAATCTCATGGG[A/G]AAGGAAGTTTAAAGT | 94253 |
rs47970060 | snp | C/T | 0.21875 | 0.248039 | intron-variant | Hecw1 | Mm_Celera | 13:14434945 | ATGCCTTTACTTATT[C/T]AGGTATCTACTCAGA | 94253 |
rs47972674 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Hecw1 | Mm_Celera | 13:14413317 | TTCTTTCAATTGTTA[A/G]TCACTGAAATTAAGC | 94253 |
rs47975733 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Hecw1 | Mm_Celera | 13:14500640 | TACAGAGCACAAAGA[A/G]ACTGGAAGACCTCAG | 94253 |
rs47992038 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Hecw1 | Mm_Celera | 13:14461755 | GATGAAGGACCAACT[C/T]ATACCATATTGTTCC | 94253 |
rs47999323 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Hecw1 | Mm_Celera | 13:14353236 | AAACCTTCCATCAGG[A/G]CATATCCTTGATAAA | 94253 |
rs48009704 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Hecw1 | Mm_Celera | 13:14272602 | ATAAGTAAGTCTAAG[C/G]TAAGGAGTATTGATT | 94253 |
rs48014949 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Hecw1 | Mm_Celera | 13:14461728 | TGATTGTGGGTAATA[C/T]GTTGAAAAGGTGATG | 94253 |
rs48015085 | snp | A/G | 0.32 | 0.24 | intron-variant | Hecw1 | Mm_Celera | 13:14238204 | TGACTTGATTTTCTG[A/G]AGTCACACTTAAGTT | 94253 |
rs48024787 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Hecw1 | Mm_Celera | 13:14469388 | TGTCTCAATTCAAGG[A/G]AAGTGGTTAATTGCT | 94253 |
rs48030384 | snp | G/T | 0.391111 | 0.206368 | intron-variant | Hecw1 | Mm_Celera | 13:14232927 | TGTACTTCTTTCTGA[G/T]CATATGCTGGTGTTT | 94253 |
rs48031723 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Hecw1 | Mm_Celera | 13:14461960 | TCAGTCCAGGCTGCA[C/T]GAGGAAGCAGTACTG | 94253 |
rs48037426 | snp | A/G | 0.473373 | 0.11227 | intron-variant | Hecw1 | Mm_Celera | 13:14421463 | AACTTCATTTAGATT[A/G]CCTTTATATTTGGAT | 94253 |
rs48053656 | snp | A/G | 0.244898 | 0.249948 | intron-variant, utr-variant-5-prime | Hecw1 | Mm_Celera | 13:14457199 | CCAAGGAACTAGCCA[A/G]TACTTTTGTTCGTTT | 94253 |
rs48070283 | snp | C/G | 0.32 | 0.24 | intron-variant | Hecw1 | Mm_Celera | 13:14246437 | TATACCTAAAAAGAA[C/G]TACAGTAGACTTGGG | 94253 |
rs48081426 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Hecw1 | Mm_Celera | 13:14357816 | CATATGTAAATGGAA[C/T]TCACAATAACATTAC | 94253 |
rs48085450 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Hecw1 | Mm_Celera | 13:14469128 | CTATCACTCAGAGCT[A/G]TTGTGGAATTTCTTG | 94253 |
rs48092110 | snp | A/G | 0.426035 | 0.177515 | intron-variant | Hecw1 | Mm_Celera | 13:14371816 | TAAGACTCTCATTAA[A/G]CCTGTCTCTGCTTTT | 94253 |
rs48101455 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Hecw1 | Mm_Celera | 13:14351801 | TCTTCTGAGCATAGA[C/T]AGAACAAAAAAGTCT | 94253 |
rs48107364 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Hecw1 | Mm_Celera | 13:14342986 | ATATTATTTATCTGT[A/T]ACTTTTCTAGGCTTC | 94253 |
rs48110009 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Hecw1 | Mm_Celera | 13:14394994 | GAATGCAAAATTGAA[C/T]CATATCCAGAGATTC | 94253 |
rs48110625 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Hecw1 | Mm_Celera | 13:14261413 | AGGAGAGAAAATGCC[C/T]CAAGTAGAATCTTAT | 94253 |
rs48127335 | snp | A/C | 0.497778 | 0.0332592 | intron-variant | Hecw1 | Mm_Celera | 13:14396035 | GCAAGTTAGACCAAT[A/C]CCTAAGGTTTGTTTG | 94253 |
rs48130334 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Hecw1 | Mm_Celera | 13:14265499 | TATCTTAGGTTAGGA[A/G]GTATCTTAAGTTAGG | 94253 |
rs48134471 | snp | A/G | 0.231111 | 0.249285 | intron-variant, upstream-variant-2KB | Hecw1 | Mm_Celera | 13:14459250 | CCTCCAGCTAACACA[A/G]TCATATTGTTTCTCT | 94253 |
rs48146836 | snp | C/G | 0.35503 | 0.226867 | intron-variant | Hecw1 | Mm_Celera | 13:14493511 | TCAACTGTTATTAAG[C/G]TGCATTATAAATAGT | 94253 |
rs48157985 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Hecw1 | Mm_Celera | 13:14263865 | ACATCAATGTCTTTG[A/G]TTATCTGTAATATCT | 94253 |
rs48173615 | snp | C/T | 0.5 | 0 | intron-variant | Hecw1 | Mm_Celera | 13:14310194 | AATTATTATTCCCCT[C/T]GGATGCGTTGGTTTT | 94253 |
rs48175230 | snp | A/T | 0.48 | 0.0979796 | intron-variant | Hecw1 | Mm_Celera | 13:14318583 | TTTTGAGCATCTCCT[A/T]TGTGAGGTTCTGGCA | 94253 |
rs48176025 | snp | C/T | 0.489796 | 0.070696 | intron-variant | Hecw1 | Mm_Celera | 13:14308341 | ATTTTGGGACTGGTT[C/T]AGATGTTATCTTGAA | 94253 |
rs48178179 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Hecw1 | Mm_Celera | 13:14277234 | TCATCTTCAGCCAGA[A/G]GGCAGAAACTTCTGA | 94253 |
rs48196611 | snp | G/T | 0.473373 | 0.11227 | intron-variant | Hecw1 | Mm_Celera | 13:14424743 | GCACAGGTTAACTCA[G/T]CAATGACCCTCTGAT | 94253 |
rs48200433 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Hecw1 | Mm_Celera | 13:14482761 | TACTAAATTCCACAG[A/G]CGTGAGGTCCTGTGC | 94253 |
rs48203405 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Hecw1 | Mm_Celera | 13:14341675 | AGGACATAAGAAAAC[A/G]AAGGGCAGTCATTTT | 94253 |
rs48203598 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Hecw1 | Mm_Celera | 13:14352625 | TTCTTTGGCTCATGG[A/G]ATGGAAAAACCACTA | 94253 |
rs48218403 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Hecw1 | Mm_Celera | 13:14461816 | AGATAGTAGGGAACA[C/T]ATTGAAATTCCCAGT | 94253 |
rs48222671 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Hecw1 | Mm_Celera | 13:14281413 | GAATAAGAAGTTTGA[A/G]GCTAGCCTAGTTCTC | 94253 |
rs48231613 | snp | A/T | | | intron-variant | Hecw1 | Mm_Celera | 13:14239693 | ACATAAACAACAGAA[A/T]CCAAGGATATTTGGC | 94253 |
rs48238671 | snp | G/T | 0.124444 | 0.216185 | intron-variant, utr-variant-5-prime | Hecw1 | Mm_Celera | 13:14455947 | GATTCCAGCTGGGTT[G/T]TGAACATCTTGGCTA | 94253 |
rs48241916 | snp | A/G | 0.32 | 0.24 | intron-variant | Hecw1 | Mm_Celera | 13:14376607 | TCTCTGTTTTAAGTG[A/G]GCGTTATTTTATTTG | 94253 |
rs48245510 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Hecw1 | Mm_Celera | 13:14395088 | AGGAGCAATAGGGGA[A/G]CATTTGATAGAAACA | 94253 |
rs48250537 | snp | A/G | 0.165289 | 0.235211 | intron-variant | Hecw1 | Mm_Celera | 13:14427444 | AGGTTACTTGATAGC[A/G]TGAGAATTAATTCTA | 94253 |
rs48255630 | snp | A/G | 0.426035 | 0.177515 | intron-variant | Hecw1 | Mm_Celera | 13:14374344 | ACTAAGGACACACAA[A/G]TTATAAACTACTAAG | 94253 |
rs48258220 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Hecw1 | Mm_Celera | 13:14320615 | GTGACAGTTCTAAAG[A/G]GAAGATGATAGTTGA | 94253 |
rs48260273 | snp | C/T | 0.18 | 0.24 | intron-variant | Hecw1 | Mm_Celera | 13:14443723 | GTCATTACAGTTTAT[C/T]CCTCAGAATCTAGTC | 94253 |
rs48262486 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Hecw1 | Mm_Celera | 13:14273920 | ATATGCAAGATGTTG[C/T]TGAACAGGGCCATGA | 94253 |
rs48265169 | snp | C/T | 0.35503 | 0.226867 | intron-variant | Hecw1 | Mm_Celera | 13:14406175 | TTAGATTTCATCCTA[C/T]CTCACGTAAGCTTTT | 94253 |
rs48266385 | snp | C/T | 0.486111 | 0.0821678 | intron-variant, utr-variant-5-prime | Hecw1 | Mm_Celera | 13:14455752 | TAGTATGTTAAGAGA[C/T]GAACATGGAAAGGAC | 94253 |
rs48269678 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Hecw1 | Mm_Celera | 13:14352564 | ACTACAGTTGAGAAA[A/G]ATGTGACATTTTGGG | 94253 |
rs48271365 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Hecw1 | Mm_Celera | 13:14394735 | AAATGGTTGTAGGAC[G/T]TTTGTCATTGTCTTG | 94253 |
rs48279830 | snp | A/G | 0.35503 | 0.226867 | intron-variant | Hecw1 | Mm_Celera | 13:14453958 | TCGGTTCTGTACATT[A/G]TACCACTATATGTAT | 94253 |
rs48286325 | snp | G/T | | | intron-variant | Hecw1 | Mm_Celera | 13:14289155 | GACAAGGAAGGGCAC[G/T]TCATACTCATCAAAG | 94253 |
rs48293235 | snp | A/C | 0.391111 | 0.206368 | intron-variant | Hecw1 | Mm_Celera | 13:14469491 | TGTACAGCATCCTAC[A/C]TGTTTCATCAGACTT | 94253 |
rs48294424 | snp | A/T | 0.48 | 0.0979796 | intron-variant | Hecw1 | Mm_Celera | 13:14424556 | CATTCTAAGAATAGA[A/T]TACTCCTAAATCTTT | 94253 |
rs48294657 | snp | A/G | 0.32 | 0.24 | intron-variant | Hecw1 | Mm_Celera | 13:14472911 | CAAATCATGTAACCA[A/G]CAGAAGTCTTTGCTT | 94253 |
rs48295587 | snp | G/T | 0.277778 | 0.248452 | intron-variant | Hecw1 | Mm_Celera | 13:14250406 | AACATGTAAACACAG[G/T]TACCTATAGTTGTTT | 94253 |
rs48327527 | snp | A/G | 0.297521 | 0.245442 | intron-variant | Hecw1 | Mm_Celera | 13:14374831 | TCTAGTATGGTCTAT[A/G]TGCTTGAGCTCTGCC | 94253 |
rs48331164 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Hecw1 | Mm_Celera | 13:14322373 | GAAAGCCCCGAAACT[A/G]GAAACCATTTTAGGT | 94253 |
rs48341499 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Hecw1 | Mm_Celera | 13:14423497 | ATTATTGTAGAAATA[A/G]CATCAAAATAGGCAA | 94253 |
rs48350893 | snp | A/G | 0.391111 | 0.206368 | utr-variant-3-prime | Hecw1 | GRCm38.p3 | 13:14230539 | CTTTTGCCAATTCTA[A/G]TTTGCTTTGAAATAA | 94253 |
rs48356910 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Hecw1 | Mm_Celera | 13:14387415 | ATTCCTGTCACTGTG[A/T]TGTTTGTTTGCTTGT | 94253 |
rs48361115 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Hecw1 | Mm_Celera | 13:14306443 | GTTAGGTATCTTTGG[A/T]AACATCTCATGATGG | 94253 |
rs48362645 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Hecw1 | Mm_Celera | 13:14490608 | GGGTCATGTTGCCTT[A/G]GTAGTAGATTAGATG | 94253 |
rs48367119 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Hecw1 | Mm_Celera | 13:14511543 | TTTGTAACAGCAAAT[A/G]GAAAGCCACATTATA | 94253 |
rs48369557 | snp | A/C | | | intron-variant | Hecw1 | Mm_Celera | 13:14284221 | CAGAATGGCTAAGAT[A/C]AAAAACTCAGGTGAC | 94253 |
rs48370722 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Hecw1 | Mm_Celera | 13:14231521 | TTTCCTGCCAGGAAC[C/T]CTTTGTTTCTATGGA | 94253 |
rs48372368 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Hecw1 | Mm_Celera | 13:14460816 | CTGGGAAATTAGCCC[G/T]GGGTTCAATCACAGG | 94253 |
rs48380789 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Hecw1 | Mm_Celera | 13:14426288 | ACACAATAAACCTAA[A/G]CCAATTTCAAACAGC | 94253 |
rs48382797 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Hecw1 | Mm_Celera | 13:14389395 | AAGACCTTGAGAGTA[C/T]AAGACAGGTCCTCTA | 94253 |
rs48382975 | snp | A/T | 0.426035 | 0.177515 | intron-variant | Hecw1 | Mm_Celera | 13:14372519 | ACACCTTTTATTTTT[A/T]AAATTTCACCAAACA | 94253 |
rs48391648 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Hecw1 | Mm_Celera | 13:14432106 | GGGGGACAAAGAGGA[C/T]AGCACATAGGCAGAT | 94253 |
rs48397699 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Hecw1 | Mm_Celera | 13:14433040 | TGCTTAATAAATTTC[C/T]ACAGCACTATGCAAT | 94253 |
rs48420822 | snp | C/T | 0.35503 | 0.226867 | utr-variant-3-prime | Hecw1 | GRCm38.p3 | 13:14227131 | GAAAAGCATTTAAAT[C/T]TTTCATAATGAAAGC | 94253 |
rs48425874 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Hecw1 | Mm_Celera | 13:14315285 | CACTGAACATTCTAG[C/T]TCTCTACTGCAATGT | 94253 |
rs48431647 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Hecw1 | Mm_Celera | 13:14472376 | AATTAAAGTCCTTTT[A/T]TACAGCCACTCATGC | 94253 |
rs48433345 | snp | A/C | 0.497778 | 0.0332592 | intron-variant | Hecw1 | Mm_Celera | 13:14357563 | TATCATATTTTACTG[A/C]AATTAATATCGTGAT | 94253 |
rs48438403 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Hecw1 | Mm_Celera | 13:14266399 | TGGATCCCGATCAGA[A/G]AGTGTGTATTTTCCA | 94253 |
rs48453898 | snp | C/T | | | intron-variant | Hecw1 | GRCm38.p3 | 13:14240979 | AAAGGGCTAGAAAAC[C/T]ATTTTCCAAGCAAAT | 94253 |
rs48468762 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Hecw1 | GRCm38.p3 | 13:14307307 | TGTTAGTGTTGTGAA[C/T]CAGCTCTTCATTCAG | 94253 |
rs48475112 | snp | A/G | 0.408163 | 0.193609 | intron-variant, utr-variant-5-prime | Hecw1 | Mm_Celera | 13:14456982 | GCAGTAAAGCACTTC[A/G]GAAGATAATGCAATA | 94253 |
rs48479278 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Hecw1 | Mm_Celera | 13:14454010 | GAGAATTAAACTCCT[A/G]TGAACCAAAGAAGGC | 94253 |
rs48486553 | snp | C/T | | | intron-variant | Hecw1 | Mm_Celera | 13:14265773 | CTTTTTCCTCCCCTT[C/T]CCTATCTTCTCCCTT | 94253 |
rs48490656 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Hecw1 | Mm_Celera | 13:14273253 | AGTAGACACAGCTGA[C/T]CTTATGGAGGTACAC | 94253 |
rs48511921 | snp | C/G | | | intron-variant | Hecw1 | Mm_Celera | 13:14387663 | TCTGCCTCCCAAGTG[C/G]TGGGATTAAAGGCGT | 94253 |
rs48525035 | snp | A/G | | | intron-variant | Hecw1 | Mm_Celera | 13:14242752 | ATAGGTTGGGAGAAA[A/G]TGGGCAGCCTTGTCT | 94253 |
rs48528393 | snp | A/G | 0.426035 | 0.177515 | intron-variant | Hecw1 | Mm_Celera | 13:14371938 | ATAGGAATGTGAAAT[A/G]TGGTGAAAGTACTCA | 94253 |
rs48529763 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Hecw1 | Mm_Celera | 13:14321738 | CACACACCCATACAT[A/G]TGCTGTCAATTACTA | 94253 |
rs48546397 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Hecw1 | Mm_Celera | 13:14344884 | GCAAGTCCTGCATGG[C/T]GGAACCATACCTGTC | 94253 |
rs48548403 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Hecw1 | Mm_Celera | 13:14238489 | ATTGAACTATAGAGG[C/T]ATCATTTTTGGGCCT | 94253 |
rs48551250 | snp | A/T | 0.297521 | 0.245442 | intron-variant | Hecw1 | Mm_Celera | 13:14375022 | TCACACTCAGTAAGT[A/T]TCAATTACTCATTAT | 94253 |
rs48558805 | snp | A/G | | | intron-variant | Hecw1 | Mm_Celera | 13:14433863 | TAGTCTCTCTCTGGG[A/G]AGGGAGTTTAGTAAC | 94253 |
rs48560710 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Hecw1 | Mm_Celera | 13:14432537 | CTCTTTGTAGCTTTT[C/T]GCAGCCAAAGAAGTG | 94253 |
rs48562747 | snp | C/T | 0.32 | 0.24 | synonymous-codon | Hecw1 | GRCm38.p3 | 13:14245765 | TGCCTCCGTCTGCTG[C/T]ACCACACCACGCTCC | 94253 |
rs48579206 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Hecw1 | Mm_Celera | 13:14358536 | TTCCTGGGTTATAAT[C/T]AAACTTACACCTAAC | 94253 |
rs48582678 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Hecw1 | Mm_Celera | 13:14348842 | CAAATTAATGAAGGG[A/G]ATACACTAAATAAAA | 94253 |
rs48584244 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Hecw1 | Mm_Celera | 13:14272194 | GAAACATGGTTAACA[G/T]CATTCCCCCAATATC | 94253 |
rs48597540 | snp | A/C/T | 0.408163 | 0.193609 | intron-variant | Hecw1 | Mm_Celera | 13:14320267 | TGATCATAAGAAAAA[A/C/T]TTTTGAATCTAAATC | 94253 |
rs48616727 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Hecw1 | Mm_Celera | 13:14339959 | AGCAAGGGCACTTAC[A/G]GTGAAATCCAGTTGT | 94253 |
rs48624998 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Hecw1 | Mm_Celera | 13:14358991 | CCTTCCCGAGTCATG[C/T]TTTTCCTGCTGGCAT | 94253 |
rs48639765 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Hecw1 | Mm_Celera | 13:14237246 | TAATCTTTATCCCCA[G/T]CTCTGGAGCCTTAAA | 94253 |
rs48640253 | snp | A/G | 0.426035 | 0.177515 | intron-variant | Hecw1 | Mm_Celera | 13:14414571 | TGAGTTATTTTTAGC[A/G]TTAGTTTAGTTACTG | 94253 |
rs48641950 | snp | A/G | 0.375 | 0.216506 | intron-variant | Hecw1 | Mm_Celera | 13:14406179 | ATTTCATCCTACCTC[A/G]CGTAAGCTTTTATGT | 94253 |
rs48661249 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Hecw1 | Mm_Celera | 13:14473013 | TAGACCCCTTTGCTA[A/G]CCATTTCAGGGGAAA | 94253 |
rs48667994 | snp | C/T | 0.32 | 0.24 | intron-variant | Hecw1 | Mm_Celera | 13:14350386 | GGGAGAAAGGAAGGG[C/T]GAATGCAGGTAATGA | 94253 |
rs48680554 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Hecw1 | Mm_Celera | 13:14341588 | GGAATGGGTGAGAGG[C/T]TGATGGTGGACATGG | 94253 |
rs48681377 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Hecw1 | Mm_Celera | 13:14311008 | AGGCTGAATTGCATT[A/G]TACAGGCAGGACTGA | 94253 |
rs48681746 | snp | A/G/T | 0.124444 | 0.216185 | intron-variant | Hecw1 | GRCm38.p3 | 13:14461162 | ACTATGTCCTTCCCT[A/G/T]TTGTGAAGGGCGTTA | 94253 |
rs48691745 | snp | A/T | 0.18 | 0.24 | intron-variant, utr-variant-5-prime | Hecw1 | Mm_Celera | 13:14455249 | TGAAAATCAACATAA[A/T]TATTTGACATGGAGT | 94253 |
rs48696616 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Hecw1 | Mm_Celera | 13:14315845 | GATATATTTCTTGGT[A/G]TGAATTTGAGACAGG | 94253 |
rs48716941 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Hecw1 | Mm_Celera | 13:14433349 | AGAAAGTGTGAGCTG[A/C]AGTTCCTGAAAACTA | 94253 |
rs48718516 | snp | A/G | 0.32 | 0.24 | intron-variant | Hecw1 | Mm_Celera | 13:14317423 | GAGCTGGTGTTCTGT[A/G]TAGGCACGTGTAAAA | 94253 |
rs48721964 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Hecw1 | Mm_Celera | 13:14262433 | AAAACTAAGGAGTTG[A/G]TGGAACAAAAACTTT | 94253 |
rs48724691 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Hecw1 | Mm_Celera | 13:14344302 | TAAAAAACTATTAAA[A/T]TTTTCTCTTCTCCTC | 94253 |
rs48729140 | snp | A/G | 0.21875 | 0.248039 | intron-variant | Hecw1 | Mm_Celera | 13:14510832 | AAATTGTATGACATA[A/G]TGTCCCATATAGCTA | 94253 |
rs48754547 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Hecw1 | Mm_Celera | 13:14491286 | AAAATAATACAGGCT[C/T]ACAACCTGGTGAATC | 94253 |
rs48756386 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Hecw1 | Mm_Celera | 13:14307703 | TAATAAAATGTGAAG[C/T]CACAATAATCAAACA | 94253 |
rs48759761 | snp | C/T | 0.35503 | 0.226867 | intron-variant | Hecw1 | Mm_Celera | 13:14423206 | GATCTGCAATGGTGC[C/T]GAATAGGAATAAATA | 94253 |
rs48762349 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Hecw1 | Mm_Celera | 13:14364831 | TCAGGGGAAAAAAAA[A/C]CATTTAGGCCTGCTG | 94253 |
rs48774362 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Hecw1 | Mm_Celera | 13:14481335 | ATGATTTCATGATGG[C/T]TGATGTTATTGACTA | 94253 |
rs48804883 | snp | G/T | 0.32 | 0.24 | intron-variant | Hecw1 | Mm_Celera | 13:14358359 | GTACAAATGTATAAT[G/T]CAATAAAAATTTCTA | 94253 |
rs48808310 | snp | A/C | 0.497778 | 0.0332592 | intron-variant | Hecw1 | Mm_Celera | 13:14492411 | TAGATCGATTGTTTT[A/C]ATAAGAACAAGTTTT | 94253 |
rs48813158 | snp | A/G | 0.142012 | 0.225474 | missense | Hecw1 | Mm_Celera | 13:14317057 | CTCAGGGTGGGCTGG[A/G]TGTCATGTTGCTCTG | 94253 |
rs48816648 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Hecw1 | Mm_Celera | 13:14364507 | TAGAGGAACCTATGA[C/T]GATGGTTGCCCACCA | 94253 |
rs48820783 | snp | A/G | 0.375 | 0.216506 | intron-variant | Hecw1 | Mm_Celera | 13:14371612 | GGCAGGACACATGGT[A/G]AGATGATATGGTTTC | 94253 |
rs48827185 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Hecw1 | Mm_Celera | 13:14233956 | GTGCTATAGGTGTAT[C/T]CTCTCTGTCAGTGGG | 94253 |
rs48827243 | snp | A/T | 0.32 | 0.24 | intron-variant | Hecw1 | Mm_Celera | 13:14467432 | TACTATGAGATCATT[A/T]TTGGGAGAGACTTGG | 94253 |
rs48827821 | snp | C/G | | | intron-variant | Hecw1 | Mm_Celera | 13:14414762 | AGGGAGGAGCCACCA[C/G]GATGGTAACTGCTGC | 94253 |
rs48830261 | snp | A/G | 0.32 | 0.24 | intron-variant | Hecw1 | Mm_Celera | 13:14248565 | GTGGTTGGATCAAGG[A/G]CCTAACATATCCTAG | 94253 |
rs48836480 | snp | A/G | 0.32 | 0.24 | intron-variant | Hecw1 | Mm_Celera | 13:14460805 | AAATTTATGGACTGG[A/G]AAATTAGCCCTGGGT | 94253 |
rs48849014 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Hecw1 | Mm_Celera | 13:14426435 | TCCCTAAACATCCTC[A/G]TGTCTTCCACACTGC | 94253 |
rs48849349 | snp | G/T | 0.375 | 0.216506 | intron-variant | Hecw1 | Mm_Celera | 13:14395571 | TTACGATGAAAGCTG[G/T]GCCTCTTGGATTCTG | 94253 |
rs48863037 | snp | A/G | 0.426035 | 0.177515 | intron-variant | Hecw1 | Mm_Celera | 13:14370751 | TATCTTTACACATTA[A/G]TCAACACCATGTTCT | 94253 |
rs48863856 | snp | A/C/G | 0.391111 | 0.206368 | intron-variant | Hecw1 | Mm_Celera | 13:14492612 | CAGGTCTTCCAACCT[A/C/G]CTAATCTTCAGGCTG | 94253 |
rs48922378 | snp | G/T | | | intron-variant | Hecw1 | Mm_Celera | 13:14239603 | CAGAGTTTTGTAGGT[G/T]GGAAAAGCCACAGTC | 94253 |
rs48936113 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Hecw1 | Mm_Celera | 13:14231310 | CCTTCCGCAAGCCTG[C/G]GAGAGTCTTCACATC | 94253 |
rs48942791 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Hecw1 | Mm_Celera | 13:14318694 | AGAGGAATCTTTCAA[C/T]CAAGGAGGCAATCCT | 94253 |
rs48960306 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Hecw1 | Mm_Celera | 13:14294157 | GGAAATGATCAGATT[C/T]CAACCAATGAAAGAA | 94253 |
rs48969994 | snp | C/T | 0.35503 | 0.226867 | intron-variant, utr-variant-5-prime | Hecw1 | Mm_Celera | 13:14455824 | CCACTGTAATTCAGC[C/T]GATTGGAGTTACCAT | 94253 |
rs48976725 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Hecw1 | Mm_Celera | 13:14233003 | CTCTCTGCTCTGTCC[C/T]GTAATGTTCACCAAA | 94253 |
rs48985068 | snp | A/T | 0.375 | 0.216506 | intron-variant | Hecw1 | Mm_Celera | 13:14424653 | TTCATGGTATATATA[A/T]AATTATGATTGTGAA | 94253 |
rs48987284 | snp | G/T | 0.473373 | 0.11227 | intron-variant | Hecw1 | Mm_Celera | 13:14414414 | TATAATGATGGTACT[G/T]GACTCTCCAATTATT | 94253 |
rs48990964 | snp | C/T | | | intron-variant | Hecw1 | Mm_Celera | 13:14415900 | AGTTGATGAAAATCT[C/T]TTCCCGTTTTGTTGA | 94253 |
rs49022012 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Hecw1 | Mm_Celera | 13:14490423 | GGGGAGATGGACCTT[C/T]TAAGTGATCAAAGGC | 94253 |
rs49023349 | snp | C/T | | | intron-variant | Hecw1 | Mm_Celera | 13:14239570 | CCTAAGAGAACTGGT[C/T]TCCTAGGAGTACTGA | 94253 |
rs49028884 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Hecw1 | Mm_Celera | 13:14352911 | GCAATATAATGTCAT[C/T]TTCCTGCTTTTCACT | 94253 |
rs49055843 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Hecw1 | Mm_Celera | 13:14427360 | AAGTGCTATAGTCTG[A/G]ACTTTAGCTTGTTTC | 94253 |
rs49060809 | snp | A/C | 0.497778 | 0.0332592 | intron-variant | Hecw1 | Mm_Celera | 13:14230933 | TTAGGAAATTGAAGA[A/C]CTAGAAACAGTTAAT | 94253 |
rs49066621 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Hecw1 | Mm_Celera | 13:14415069 | TGAAAGAAATAGTGG[A/G]AGGAAAAATTGTTGA | 94253 |
rs49071195 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Hecw1 | Mm_Celera | 13:14426568 | TTTACAAGTAGTCAC[C/G]GGCCATACAACTCTT | 94253 |
rs49073048 | snp | G/T | 0.391111 | 0.206368 | intron-variant | Hecw1 | Mm_Celera | 13:14253357 | AGAAGGCTGTGGCTG[G/T]CAGGCACCTTCGTGT | 94253 |
rs49079129 | snp | C/G | | | intron-variant | Hecw1 | Mm_Celera | 13:14511998 | AGTCAATGCTAGCTT[C/G]TCAAACATAAGAGTG | 94253 |
rs49082345 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Hecw1 | Mm_Celera | 13:14234256 | AATAGGAAAGCATGC[C/T]TTTTCTCTGCAGAGT | 94253 |
rs49086959 | snp | C/G | 0.32 | 0.24 | intron-variant | Hecw1 | Mm_Celera | 13:14351139 | TTCAAACAAAAATGT[C/G]TTCTAAAATTGTCAT | 94253 |
rs49094138 | snp | A/C | 0.444444 | 0.157135 | utr-variant-3-prime | Hecw1 | GRCm38.p3 | 13:14227025 | CTATTGATGAAACTG[A/C]ATATTGTTAGACATT | 94253 |
rs49095266 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Hecw1 | Mm_Celera | 13:14344358 | ACACATGATAATATC[C/T]GGATTCACTATTAAA | 94253 |
rs49096839 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Hecw1 | Mm_Celera | 13:14454082 | CAAGACCAGATGAAA[A/C]AGGTAATTTCTGAGC | 94253 |
rs49097620 | snp | C/T | 0.473373 | 0.11227 | intron-variant | Hecw1 | Mm_Celera | 13:14414378 | TTATACAGTGATGAG[C/T]AAAGTTATCAAATAA | 94253 |
rs49102474 | snp | C/T | 0.426035 | 0.177515 | intron-variant | Hecw1 | Mm_Celera | 13:14371154 | ACACATGGCCTGGTG[C/T]AACAGCTTGCTTCTG | 94253 |
rs49103492 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Hecw1 | Mm_Celera | 13:14325867 | TATGGTGAATTCAGG[A/G]TGCTTAGCTTTTCCC | 94253 |
rs49108951 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Hecw1 | Mm_Celera | 13:14273015 | GCAGACCATGGGAGA[A/C]CCCAGAACAGCTGCA | 94253 |
rs49112554 | snp | C/T | 0.32 | 0.24 | intron-variant | Hecw1 | Mm_Celera | 13:14389802 | TATCATCAGTAGGTC[C/T]TTCCAAGCACATGAG | 94253 |
rs49116464 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Hecw1 | Mm_Celera | 13:14360927 | GGTCTGTTTGTTACT[C/G]AGCTTTGTTAATTAG | 94253 |
rs49125319 | snp | A/C | 0.124444 | 0.216185 | intron-variant, utr-variant-5-prime | Hecw1 | Mm_Celera | 13:14456601 | ACTTGTCTGTGAAAA[A/C]GGAGTAGGAGAGAAA | 94253 |
rs49135899 | snp | A/G | 0.444444 | 0.157135 | utr-variant-3-prime | Hecw1 | GRCm38.p3 | 13:14227782 | TGGATGAAGTGGGAC[A/G]TGTCTATCCATGACT | 94253 |
rs49147303 | snp | C/T | 0.35503 | 0.226867 | intron-variant | Hecw1 | Mm_Celera | 13:14374252 | GACAGGTCAGATGAA[C/T]AACTACTCACCCTAC | 94253 |
rs49160352 | snp | A/C | 0.142012 | 0.225474 | intron-variant | Hecw1 | Mm_Celera | 13:14415224 | GAAGGGCTAGGAAAA[A/C]AGAATCATGCCACCG | 94253 |
rs49163140 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Hecw1 | Mm_Celera | 13:14364878 | AGTCCACTCACTAGT[C/T]ATGGCATCTCAGAAC | 94253 |
rs49171336 | snp | C/T | 0.32 | 0.24 | intron-variant | Hecw1 | Mm_Celera | 13:14251923 | TGCCAACTCACAGAA[C/T]GAAACAATGTAAGGC | 94253 |
rs49177489 | snp | A/T | 0.391111 | 0.206368 | intron-variant | Hecw1 | Mm_Celera | 13:14344502 | GTAATTTGATAATCT[A/T]AGGTCACAGTTTTCT | 94253 |
rs49182259 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Hecw1 | Mm_Celera | 13:14460231 | GAGCCACTGGGCGTA[A/G]CTGTCAGTCACTTTC | 94253 |
rs49184238 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Hecw1 | Mm_Celera | 13:14301018 | CTAAATTCAAACTCA[C/T]GACCTTCTAGTCTCT | 94253 |
rs49197145 | snp | A/G | 0.426035 | 0.177515 | intron-variant | Hecw1 | Mm_Celera | 13:14371496 | ATGCAATTGCAGCAA[A/G]ATCCAGAAGCTGACA | 94253 |
rs49202265 | snp | G/T | 0.391111 | 0.206368 | intron-variant | Hecw1 | Mm_Celera | 13:14307602 | CCCCAAAAGCTTCTT[G/T]CAAAACTGAGCAGGC | 94253 |
rs49210067 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Hecw1 | Mm_Celera | 13:14466594 | CTTGTCAATACTAAA[A/G]ATTAAATCCCTGTTG | 94253 |
rs49219327 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Hecw1 | Mm_Celera | 13:14294109 | ACTGACAAGGTGACG[C/T]GAACATAGAAAACAG | 94253 |
rs49223276 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Hecw1 | Mm_Celera | 13:14319644 | CTGAGCTATGGAAAG[C/T]CCCCTGGTAGAGGAT | 94253 |
rs49224131 | snp | A/G | 0.32 | 0.24 | intron-variant | Hecw1 | Mm_Celera | 13:14348237 | GGTTTACAGATAATG[A/G]GACTTAAGGAAAATC | 94253 |
rs49239191 | snp | C/T | | | intron-variant | Hecw1 | Mm_Celera | 13:14444621 | GACCTTTGGGAGTGT[C/T]TGCTATGACAGAACA | 94253 |
rs49243851 | snp | A/G | | | intron-variant | Hecw1 | Mm_Celera | 13:14242717 | AGAAGCTGGAAGCAA[A/G]CCCACTAAAATCAGG | 94253 |
rs49249553 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Hecw1 | Mm_Celera | 13:14232138 | AAGGACTTGATTTGG[A/G]GAAAAAACATGAAAA | 94253 |
rs49252890 | snp | A/G | 0.426035 | 0.177515 | intron-variant, upstream-variant-2KB | Hecw1 | Mm_Celera | 13:14458125 | AGCTGTGACAACTCT[A/G]CTGCATATCGTCATA | 94253 |
rs49261959 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Hecw1 | Mm_Celera | 13:14434075 | ATAGAAAGTACCCAT[A/G]TTGACTGTTTCATAA | 94253 |
rs49270713 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Hecw1 | Mm_Celera | 13:14353554 | GTGTCCTTCAGGCCT[A/C]GCACAACTTAGATGT | 94253 |
rs49276450 | snp | C/T | | | intron-variant | Hecw1 | Mm_Celera | 13:14267446 | GATGATATGATAGTA[C/T]ATATAAGTGAGCCTA | 94253 |
rs49277068 | snp | A/G | 0.297521 | 0.245442 | intron-variant | Hecw1 | Mm_Celera | 13:14422429 | AATAGACTTACACTG[A/G]TTATAAGCAGGTGAC | 94253 |
rs49278059 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Hecw1 | Mm_Celera | 13:14481845 | AAATAGAAATTTCAT[A/G]CTCATAGGCTACCAG | 94253 |
rs49283561 | snp | C/T | 0.426035 | 0.177515 | intron-variant | Hecw1 | Mm_Celera | 13:14426098 | AACATATTAGTAAAA[C/T]TTAGACAAGAAACCT | 94253 |
rs49295541 | snp | A/T | 0.336735 | 0.234472 | intron-variant | Hecw1 | Mm_Celera | 13:14502145 | GCTTTCACGGTGATA[A/T]ATAGACCATGCAAGC | 94253 |
rs49295806 | snp | C/T | 0.486111 | 0.0821678 | intron-variant | Hecw1 | Mm_Celera | 13:14421943 | CTAAAAGTGTACTTC[C/T]GAACTCTAGGGAATT | 94253 |
rs49297901 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Hecw1 | Mm_Celera | 13:14459876 | ATTCTCACTACCACA[A/T]TGGTTTCTTAAAATG | 94253 |
rs49301945 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Hecw1 | Mm_Celera | 13:14332737 | GAATATAAATGGTAA[A/G]CCTTCTGGTGCCAGG | 94253 |
rs49324186 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Hecw1 | Mm_Celera | 13:14265341 | TAGCTTCTAAGGAGA[A/G]AGGAAAAGACAGACA | 94253 |
rs49332531 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Hecw1 | Mm_Celera | 13:14345134 | TGGCTCCAATAAACT[C/T]AGTCATTTATTATTG | 94253 |
rs49340723 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Hecw1 | Mm_Celera | 13:14460590 | AGGCTACTTCGCATG[C/T]GACTTTCCATGTCAT | 94253 |
rs49345640 | snp | A/G | 0.426035 | 0.177515 | intron-variant | Hecw1 | Mm_Celera | 13:14422403 | CTGTCTGAACACAGG[A/G]AAAGCCAGTAAATAG | 94253 |
rs49366791 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Hecw1 | Mm_Celera | 13:14429942 | CCTCTTGTGTATTTA[C/T]GCTCAGTTCAGTAGA | 94253 |
rs49366826 | snp | A/G | 0.297521 | 0.245442 | intron-variant | Hecw1 | Mm_Celera | 13:14504544 | CTGGGCAAAGGATAA[A/G]TTCCCAGTCAGAAGG | 94253 |
rs49374140 | snp | A/G | | | intron-variant | Hecw1 | Mm_Celera | 13:14475791 | AAGCATTTCTAAGAG[A/G]GAGACTCATAGCTCT | 94253 |
rs49374238 | snp | G/T | 0.32 | 0.24 | intron-variant | Hecw1 | Mm_Celera | 13:14473369 | GCTGATTACTTGCAG[G/T]ATCTAAACCATAACT | 94253 |
rs49377120 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Hecw1 | Mm_Celera | 13:14503309 | GCACAATGCTGGCCA[C/T]TCTTCCGAAGCAGGC | 94253 |
rs49378185 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Hecw1 | Mm_Celera | 13:14340300 | CCTAGAAATCACCTG[C/T]AGATGAAAGCTTATG | 94253 |
rs49378323 | snp | A/G | | | intron-variant | Hecw1 | GRCm38.p3 | 13:14318221 | TGAGTTCTCAGTAAT[A/G]CAGTAACAGTAACTC | 94253 |
rs49378580 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Hecw1 | Mm_Celera | 13:14430472 | AGGAAAGGAAGAAAA[C/T]TCTGCCCTATTTCTT | 94253 |
rs49381165 | snp | A/T | 0.426035 | 0.177515 | intron-variant | Hecw1 | Mm_Celera | 13:14374430 | GTGTTGCCATTCAGC[A/T]TTAAATAGCATCACA | 94253 |
rs49382209 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Hecw1 | Mm_Celera | 13:14427179 | CACTCTCATCTCACA[A/G]ATTCTTTCTTTTTTG | 94253 |
rs49384287 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Hecw1 | Mm_Celera | 13:14264581 | TATACAAGCTTACAA[A/G]TCAATTTCATTTGCC | 94253 |
rs49417972 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Hecw1 | Mm_Celera | 13:14233104 | TCACATTGCTTTAAG[C/T]ACCTTGAATTCCTCT | 94253 |
rs49429266 | snp | C/T | | | intron-variant | Hecw1 | Mm_Celera | 13:14386662 | CTGCTCTGGCAGGGC[C/T]CTCTCAGGCGGACAC | 94253 |
rs49430438 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Hecw1 | Mm_Celera | 13:14344535 | TTGTGGTCAGTAGAA[C/T]TTGGGTTTTATGCAA | 94253 |
rs49436355 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Hecw1 | Mm_Celera | 13:14236293 | CCATGACATGCCAAG[A/G]ATTACTGTTGCCTGA | 94253 |
rs49439469 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Hecw1 | Mm_Celera | 13:14359337 | GAAAATGATTGCAAC[A/G]CCTTTGAACAAATGC | 94253 |
rs49441031 | snp | C/G | 0.391111 | 0.206368 | intron-variant | Hecw1 | Mm_Celera | 13:14432079 | ACTGGGCAATAAGCC[C/G]TCTTAGCCTCTGGGG | 94253 |
rs49441818 | snp | A/G | 0.32 | 0.24 | intron-variant, utr-variant-5-prime | Hecw1 | Mm_Celera | 13:14455462 | GTGCAAGTGGAGAAG[A/G]TTCTGTACTTTGTTA | 94253 |
rs49443380 | snp | C/T | | | intron-variant | Hecw1 | Mm_Celera | 13:14239602 | ACAGAGTTTTGTAGG[C/T]GGGAAAAGCCACAGT | 94253 |
rs49443629 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Hecw1 | Mm_Celera | 13:14431856 | TTCTAAGTGTCTATT[C/T]GAACCTGTCAGTTAT | 94253 |
rs49446811 | snp | C/T | 0.375 | 0.216506 | intron-variant | Hecw1 | Mm_Celera | 13:14414717 | TGAGGAAAGACAAAT[C/T]ACTGCTTTATGAACA | 94253 |
rs49456961 | snp | A/G | 0.459184 | 0.136902 | intron-variant, utr-variant-5-prime | Hecw1 | Mm_Celera | 13:14456813 | CTGAGGCAGCACAGT[A/G]AGTCCCAGCTAGGAA | 94253 |
rs49458346 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Hecw1 | Mm_Celera | 13:14236190 | ACAAAGAAGGCTAAC[A/G]TTTCACAGGAAGCAA | 94253 |
rs49464927 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Hecw1 | Mm_Celera | 13:14469323 | TCACAGTGTGGCCTC[A/G]TTGACTTGTAAGGAG | 94253 |
rs49467656 | snp | C/G | 0.244898 | 0.249948 | intron-variant | Hecw1 | Mm_Celera | 13:14482854 | TTATTAGGAAGTAGT[C/G]TTTGTTGCTACTTAA | 94253 |
rs49472179 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Hecw1 | Mm_Celera | 13:14305518 | GCCAACTTCATGCTT[C/T]TAAAACATCATTATT | 94253 |
rs49472965 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Hecw1 | Mm_Celera | 13:14231279 | CACCCAAGGACCACT[A/G]AGCATGTGGGACACT | 94253 |
rs49473415 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Hecw1 | Mm_Celera | 13:14497816 | AGTGGGAAGTAATGA[A/G]TATGGTCTTAGGAGT | 94253 |
rs49477387 | snp | C/T | 0.396694 | 0.202437 | intron-variant, utr-variant-5-prime | Hecw1 | Mm_Celera | 13:14457237 | ACTGAAAAAAATTAA[C/T]GATAAATGACCAGAC | 94253 |
rs49479585 | snp | C/T | 0.124444 | 0.216185 | intron-variant, utr-variant-5-prime | Hecw1 | Mm_Celera | 13:14455379 | CCATACTCTGTAAAA[C/T]AGTGTCTTCAGACTG | 94253 |
rs49480756 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Hecw1 | Mm_Celera | 13:14517695 | AAATTTCATCCACTG[C/T]ATTCATCCAAAAATA | 94253 |
rs49481645 | snp | A/G | | | intron-variant | Hecw1 | Mm_Celera | 13:14258900 | TTGAGTTGGAAATTT[A/G]ATGGGGATTGCATTG | 94253 |
rs49489308 | snp | G/T | 0.336735 | 0.234472 | intron-variant | Hecw1 | Mm_Celera | 13:14246508 | ACGATGCAAAGCACA[G/T]AGAATCAGAGAGGTC | 94253 |
rs49489917 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Hecw1 | Mm_Celera | 13:14394932 | AGACATCCCCTGTGG[A/G]CTTAAAGGCTAGATA | 94253 |
rs49502987 | snp | A/G | 0.152778 | 0.230321 | intron-variant, upstream-variant-2KB | Hecw1 | Mm_Celera | 13:14458098 | ACTGGAGCTGTCTCA[A/G]TCAGTTGAAGCAGCT | 94253 |
rs49511607 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Hecw1 | Mm_Celera | 13:14377219 | TGATTGTGCTTGTAT[G/T]TACATTGTAGAGTGA | 94253 |
rs49512044 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Hecw1 | Mm_Celera | 13:14272630 | ATTTTGCTCCAATTG[A/G]CTTTTCAATTTGTTT | 94253 |
rs49512966 | snp | C/T | | | intron-variant | Hecw1 | GRCm38.p3 | 13:14241971 | AAATGAAAAGGGAGA[C/T]ATTGCAATGGAAATG | 94253 |
rs49514203 | snp | C/T | | | intron-variant | Hecw1 | Mm_Celera | 13:14476363 | TAGCCCAGGACCAGA[C/T]GGGTTTAGTGCAGAG | 94253 |
rs49517689 | snp | C/G | | | intron-variant | Hecw1 | Mm_Celera | 13:14433578 | TGGCAACTCAAGTGA[C/G]CTAGGAGAGGGCCAG | 94253 |
rs49522987 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Hecw1 | Mm_Celera | 13:14426376 | GACTCTCAGTTCTGG[A/G]TCCACATAAAAGAAA | 94253 |
rs49523164 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Hecw1 | GRCm38.p3 | 13:14465764 | GTAAAATTATTAAGA[A/G]TTTTCTGACACATGA | 94253 |
rs49529348 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Hecw1 | Mm_Celera | 13:14468523 | GTTAGCCATGGCTTA[C/T]ATAGTACCTTGAGTT | 94253 |
rs49529819 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Hecw1 | Mm_Celera | 13:14425781 | GTCTGCAAGCCACTC[A/G]AAGAAACAAACATAC | 94253 |
rs49534131 | snp | A/G | 0.473373 | 0.11227 | intron-variant | Hecw1 | Mm_Celera | 13:14415289 | AAACAAAATTACAGA[A/G]AGAATAGAACCATAC | 94253 |
rs49537746 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Hecw1 | Mm_Celera | 13:14491413 | CTTTCTCTTTATCCA[C/T]AAAATTAGGACACAT | 94253 |
rs49539302 | snp | G/T | | | intron-variant | Hecw1 | GRCm38.p3 | 13:14244538 | AGGACACACATGATG[G/T]GCACTCACTGATAAG | 94253 |
rs49566763 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Hecw1 | Mm_Celera | 13:14491527 | TCAGTCCAAATAAAC[A/G]TTCTTTTACATATCT | 94253 |
rs49571165 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Hecw1 | Mm_Celera | 13:14279724 | GGACTGGTAGGTAGA[C/T]TATGACACATTGTAT | 94253 |
rs49576417 | snp | C/T | 0.408163 | 0.193609 | missense | Hecw1 | GRCm38.p3 | 13:14317282 | TCTCCATTGCTGTTT[C/T]CCACCATACTATTCA | 94253 |
rs49585398 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Hecw1 | Mm_Celera | 13:14492242 | TTGAGATTTCTAGTG[A/G]AGTATATTTCAATGT | 94253 |
rs49588861 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Hecw1 | Mm_Celera | 13:14496493 | GTTTTTAAATGGTGA[C/T]TCTGTCAATTGGATT | 94253 |
rs49594992 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Hecw1 | Mm_Celera | 13:14473050 | CATTTGAACAGGGTC[C/T]TAAATGATTAAAATA | 94253 |
rs49602474 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Hecw1 | Mm_Celera | 13:14318776 | ACTACACAGCCCATG[A/G]CATGCTTGGAGAGAA | 94253 |
rs49608503 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Hecw1 | Mm_Celera | 13:14428797 | TGAAAAGTCATAGGT[A/G]AAGGAAATAAGAACT | 94253 |
rs49631584 | snp | G/T | | | intron-variant | Hecw1 | Mm_Celera | 13:14464644 | GGGGGGGCTGGCTGG[G/T]TGATATTGTTCTTCC | 94253 |
rs49632364 | snp | A/G | 0.444444 | 0.157135 | utr-variant-3-prime | Hecw1 | GRCm38.p3 | 13:14227869 | CGTGTTGGGCTCTGC[A/G]AAGCAAGCTTTACAT | 94253 |
rs49649595 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Hecw1 | Mm_Celera | 13:14433234 | ATTCCAGCCTGAGAA[A/G]CTCAGCTCCTTCTCA | 94253 |
rs49650940 | snp | A/G | 0.473373 | 0.11227 | intron-variant | Hecw1 | Mm_Celera | 13:14422529 | CTGGTTTACACTCAG[A/G]AATCAATGTTCTCAA | 94253 |
rs49653965 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Hecw1 | Mm_Celera | 13:14298246 | AAAAAGGTCATCAGC[C/T]TAGTGTTTCTGACAT | 94253 |
rs49655730 | snp | A/G | 0.426035 | 0.177515 | intron-variant | Hecw1 | Mm_Celera | 13:14424801 | ATGCTCAATTCTCTA[A/G]TAATTATGCACATTG | 94253 |
rs49658527 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Hecw1 | Mm_Celera | 13:14272388 | GTATATTGGAAGTCA[C/T]GAGAGGACAAAGTGA | 94253 |
rs49662063 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Hecw1 | Mm_Celera | 13:14344051 | TGTTACTTTTTAAGC[A/C]TTTCAATGGGAACAT | 94253 |
rs49667389 | snp | C/T | | | intron-variant | Hecw1 | Mm_Celera | 13:14414199 | TGGTTATAACTTAAG[C/T]CAGTTCCCTCTTTTG | 94253 |
rs49672572 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Hecw1 | Mm_Celera | 13:14249751 | GTGAGGAACAGTTCT[A/G]TGCAATCGCAATGTG | 94253 |
rs49680974 | snp | C/T | 0.231111 | 0.249285 | intron-variant, utr-variant-5-prime | Hecw1 | Mm_Celera | 13:14457202 | AGGAACTAGCCAATA[C/T]TTTTGTTCGTTTTAA | 94253 |
rs49686786 | snp | G/T | 0.336735 | 0.234472 | intron-variant | Hecw1 | Mm_Celera | 13:14358337 | ACCTTAGCAAACAAC[G/T]GTTCAAGTACAAATG | 94253 |
rs49698608 | snp | C/G | 0.260355 | 0.249785 | intron-variant | Hecw1 | Mm_Celera | 13:14346551 | ATAAGATGCAAAGTA[C/G]CCGCTGCTTGGCGCC | 94253 |
rs49705261 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Hecw1 | Mm_Celera | 13:14482763 | CTAAATTCCACAGGC[A/G]TGAGGTCCTGTGCCT | 94253 |
rs49712113 | snp | G/T | 0.336735 | 0.234472 | intron-variant | Hecw1 | Mm_Celera | 13:14352567 | ACAGTTGAGAAAAAT[G/T]TGACATTTTGGGATT | 94253 |
rs49716625 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Hecw1 | Mm_Celera | 13:14460922 | AAGTTCAAAGCCAAG[C/T]TCAGCAGTACAGGGA | 94253 |
rs49720506 | snp | G/T | 0.408163 | 0.193609 | intron-variant | Hecw1 | Mm_Celera | 13:14481361 | GACTAGTGAGAAAAT[G/T]ATTATAAAAAATCAA | 94253 |
rs49729016 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Hecw1 | Mm_Celera | 13:14348368 | ATTTCTTAAGCTTTT[G/T]CTAACTTTATTGAAT | 94253 |
rs49730636 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Hecw1 | Mm_Celera | 13:14352453 | GGACATGTTCTAAGT[C/T]TTCCTGTTTACGAAA | 94253 |
rs49731800 | snp | C/T | | | intron-variant | Hecw1 | GRCm38.p3 | 13:14240929 | TGCATACAGGAAACA[C/T]ACCTTGGTGTCAAAG | 94253 |
rs49739043 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Hecw1 | Mm_Celera | 13:14479086 | CTAAGACTCAGAACT[A/G]TGTAAGAATAAATTT | 94253 |
rs49739060 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Hecw1 | Mm_Celera | 13:14390201 | ACATCTACAACCCTC[C/T]AAAGGAGCAAAGTAT | 94253 |
rs49746220 | snp | C/G | 0.277778 | 0.248452 | intron-variant | Hecw1 | Mm_Celera | 13:14496435 | CTACTTTAAGAAACT[C/G]TTCATTAAAATATAA | 94253 |
rs49759034 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Hecw1 | Mm_Celera | 13:14250847 | CTCCAAGGGATAGAA[A/C]GTTCTTCCACAAATT | 94253 |
rs49772777 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Hecw1 | Mm_Celera | 13:14340464 | TTTAAAATTTCTAGA[C/T]GCTTGGATTGAATTT | 94253 |
rs49787258 | snp | A/T | 0.132653 | 0.220748 | intron-variant | Hecw1 | Mm_Celera | 13:14388672 | CTATTCCAAAGTGAG[A/T]GAAAGAGGAAGCCGT | 94253 |
rs49788172 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Hecw1 | Mm_Celera | 13:14235013 | GGTTCTGTTGAAGAA[A/G]CTAGGTTTATGAGAA | 94253 |
rs49794955 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Hecw1 | Mm_Celera | 13:14246506 | CTACGATGCAAAGCA[A/C]AGAGAATCAGAGAGG | 94253 |
rs49795085 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Hecw1 | Mm_Celera | 13:14237223 | TCTTCCATTCTACTT[A/G]CATGTTATAATCTTT | 94253 |
rs49802544 | snp | A/C | | | intron-variant | Hecw1 | Mm_Celera | 13:14386675 | GCCCTCTCAGGCGGA[A/C]ACCTCTCCTCTGATG | 94253 |
rs49811211 | snp | C/T | 0.124444 | 0.216185 | intron-variant, utr-variant-5-prime | Hecw1 | Mm_Celera | 13:14455512 | AACACTAGCTACAGG[C/T]ACTGATAAATAACTT | 94253 |
rs49819536 | snp | A/G | 0.444444 | 0.157135 | utr-variant-3-prime | Hecw1 | GRCm38.p3 | 13:14230150 | TGGCCTTGGCTGTCC[A/G]TTTGGATAGAATGAA | 94253 |
rs49832053 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Hecw1 | Mm_Celera | 13:14318549 | ATTCATTTACTCATG[A/T]ATAGAATGATTAAAC | 94253 |
rs49834232 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Hecw1 | Mm_Celera | 13:14468489 | CTAGTGGTAAAAATG[C/G]AATTGGCTGATCTAT | 94253 |
rs49835664 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Hecw1 | Mm_Celera | 13:14425780 | AGTCTGCAAGCCACT[C/T]GAAGAAACAAACATA | 94253 |
rs49850286 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Hecw1 | Mm_Celera | 13:14492601 | CTGAGTTTTTTCAGG[C/T]CTTCCAACCTGCTAA | 94253 |
rs49856801 | snp | A/G | | | synonymous-codon | Hecw1 | GRCm38.p3 | 13:14247604 | GGTGAGATCTAGAAT[A/G]TCTGTGATGTTGTTG | 94253 |
rs49860189 | snp | C/T | 0.408163 | 0.193609 | intron-variant, utr-variant-5-prime | Hecw1 | Mm_Celera | 13:14455435 | GATAGCAGCATTTGG[C/T]TCCGTTTTTGAGTGC | 94253 |
rs49864726 | snp | A/G/T | 0.459184 | 0.136902 | intron-variant | Hecw1 | GRCm38.p3 | 13:14299411 | TTTGTTTCCAAGGAA[A/G/T]GTTCACTAACATGAT | 94253 |
rs49866336 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Hecw1 | Mm_Celera | 13:14357297 | CATAGTTCAAGGGGA[A/G]CTCTCCAGCAACTGC | 94253 |
rs49867938 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Hecw1 | Mm_Celera | 13:14379977 | AGACTTGGAGTCAGT[C/T]GTATCTCTTACAGGC | 94253 |
rs49868643 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Hecw1 | Mm_Celera | 13:14322661 | AACTAACTGAGAGGT[C/T]ATAGGGTTTGACAGT | 94253 |
rs49876736 | snp | A/C | | | intron-variant | Hecw1 | Mm_Celera | 13:14452199 | TGGACCCCAGAAAAT[A/C]ACATAACCCCATTCA | 94253 |
rs49878740 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Hecw1 | Mm_Celera | 13:14432509 | AGATGCCATTTGGTG[C/T]TTTTAAAGGATTCTC | 94253 |
rs49883381 | snp | A/G | 0.426035 | 0.177515 | intron-variant | Hecw1 | Mm_Celera | 13:14371745 | TAAAAGAGTGGCATG[A/G]GTGGATTTGCTTGGC | 94253 |
rs49891611 | snp | A/G | | | intron-variant | Hecw1 | Mm_Celera | 13:14239684 | AAGGCAAGAACATAA[A/G]CAACAGAATCCAAGG | 94253 |
rs49894987 | snp | G/T | 0.345679 | 0.230967 | intron-variant | Hecw1 | Mm_Celera | 13:14396095 | TGTGTGCATGCTTTT[G/T]TTGTTTTGTTCTCAT | 94253 |
rs49912882 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Hecw1 | Mm_Celera | 13:14472550 | AAGTCCTCCTAGCAA[C/T]CACTCCCTTATTTCG | 94253 |
rs49913433 | snp | C/T | 0.336735 | 0.234472 | intron-variant, utr-variant-5-prime | Hecw1 | Mm_Celera | 13:14455226 | ACAGACACATTTGCA[C/T]AGCCTGTTGAAAATC | 94253 |
rs49923926 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Hecw1 | Mm_Celera | 13:14426134 | AAAATGGTCAAAGTT[C/G]TCATCCACCATTATC | 94253 |
rs49937754 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Hecw1 | Mm_Celera | 13:14248214 | TGCCTTTCTATTGCA[C/T]TAAAATGTATGCAAG | 94253 |
rs49955822 | snp | C/T | 0.444444 | 0.157135 | synonymous-codon | Hecw1 | GRCm38.p3 | 13:14265166 | CTGGAGCTCCTTCCT[C/T]GAGTATGCCATCACT | 94253 |
rs49985879 | snp | C/G | | | intron-variant | Hecw1 | Mm_Celera | 13:14233543 | AGACATAGTAACACA[C/G]AATGGGAAAAAGTTC | 94253 |
rs49993029 | snp | A/G | 0.426035 | 0.177515 | intron-variant | Hecw1 | Mm_Celera | 13:14414810 | TGCTTTCTTTTAGAT[A/G]CCCAGAAGTTTAGGA | 94253 |
rs50005040 | snp | C/T | 0.165289 | 0.235211 | intron-variant | Hecw1 | Mm_Celera | 13:14422029 | ATTAGTAGAAGCAGA[C/T]TCTTTCCCAAATGAG | 94253 |
rs50014172 | snp | A/T | 0.32 | 0.24 | intron-variant | Hecw1 | Mm_Celera | 13:14426282 | CTCACTACACAATAA[A/T]CCTAAACCAATTTCA | 94253 |
rs50020871 | snp | A/C | 0.391111 | 0.206368 | intron-variant | Hecw1 | Mm_Celera | 13:14348729 | TTCAAGGTATATGTG[A/C]TATGATACAAAAGTT | 94253 |
rs50022904 | snp | C/T | 0.408163 | 0.193609 | intron-variant, utr-variant-5-prime | Hecw1 | Mm_Celera | 13:14455347 | TAAGATCAGTTTGTT[C/T]CCTGCTCTCAGTTAC | 94253 |
rs50023835 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Hecw1 | Mm_Celera | 13:14413657 | TTCAGCAAGACCTCA[A/T]GTACTAAACAGTGTT | 94253 |
rs50027911 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Hecw1 | Mm_Celera | 13:14472893 | CTGACAAATATTTCC[C/T]GGCAAATCATGTAAC | 94253 |
rs50040229 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Hecw1 | Mm_Celera | 13:14480867 | GTATTTGTGAGCCTC[C/T]TTGAGACCAAGCCAC | 94253 |
rs50041635 | snp | G/T | | | intron-variant | Hecw1 | Mm_Celera | 13:14257686 | GGTCTCATTTGTTGA[G/T]TCTTGATCTTACCTC | 94253 |
rs50049017 | snp | C/T | 0.124444 | 0.216185 | intron-variant, upstream-variant-2KB | Hecw1 | Mm_Celera | 13:14458231 | GTTCCTTATGTCCCA[C/T]CACAAAGAAGTGTGT | 94253 |
rs50049767 | snp | A/G | 0.5 | 0 | intron-variant | Hecw1 | Mm_Celera | 13:14345213 | CAGCCAGGGTTAATA[A/G]ACCTTTACCTAGACT | 94253 |
rs50050050 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Hecw1 | Mm_Celera | 13:14318422 | ATCTTTATTTTTCCT[C/G]TAATTGTCTAACTGC | 94253 |
rs50059099 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Hecw1 | Mm_Celera | 13:14378412 | CATTCCTGATGCATT[C/T]AATCCTCCATACAGT | 94253 |
rs50061006 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Hecw1 | Mm_Celera | 13:14353422 | GCATTGGAAAAATGC[A/G]ACCAGGCAAGGATGC | 94253 |
rs50073527 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Hecw1 | Mm_Celera | 13:14307444 | TGATTTATTTTTCTT[C/T]TATGTGCATTGGTGT | 94253 |
rs50081259 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Hecw1 | Mm_Celera | 13:14468890 | CAATGTGTCAGACCA[C/T]CTTCCAGGATGAGCC | 94253 |
rs50087169 | snp | C/G | 0.473373 | 0.11227 | intron-variant | Hecw1 | Mm_Celera | 13:14422136 | ACCTTTGTTGACATA[C/G]TTTTTTCCACATTGT | 94253 |
rs50091179 | snp | C/G | 0.18 | 0.24 | intron-variant | Hecw1 | Mm_Celera | 13:14372308 | ACAACTAGTGCAATG[C/G]CTCTTAAATTATTTT | 94253 |
rs50101186 | snp | A/G/T | | | intron-variant | Hecw1 | Mm_Celera | 13:14253668 | TACCCACCCTCTACC[A/G/T]CCTCCCTGCCCTTAA | 94253 |
rs50101678 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Hecw1 | Mm_Celera | 13:14265658 | TACTTTTACATGAAT[A/G]GAAATATAAGATTTT | 94253 |
rs50104325 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Hecw1 | Mm_Celera | 13:14319937 | TGGGATATCCAGGTA[C/T]AAAAAAAGGCATAGT | 94253 |
rs50122335 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Hecw1 | Mm_Celera | 13:14350430 | AAGAAGACATAAGAC[G/T]AATTGTTTTCTAGGT | 94253 |
rs50125469 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Hecw1 | Mm_Celera | 13:14482470 | ACAGCACAGGTCCCT[A/G]GCAGCTCATACCACT | 94253 |
rs50126650 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Hecw1 | Mm_Celera | 13:14361578 | GTGAACACATGAATG[A/G]CCTTTATGATCAGTA | 94253 |
rs50130299 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Hecw1 | Mm_Celera | 13:14231262 | GAAGCTTACATGGCC[C/T]ACACCCAAGGACCAC | 94253 |
rs50139595 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Hecw1 | Mm_Celera | 13:14469304 | TGAACTTTCAGCCAG[C/T]CATTCACAGTGTGGC | 94253 |
rs50160746 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Hecw1 | Mm_Celera | 13:14233134 | TGATTCTCCCTTATG[C/T]TGAAATTAGTTATCT | 94253 |
rs50161383 | snp | A/T | 0.408163 | 0.193609 | intron-variant | Hecw1 | Mm_Celera | 13:14482746 | TTCAAATGGTTGAAG[A/T]ACTAAATTCCACAGG | 94253 |
rs50162315 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Hecw1 | Mm_Celera | 13:14237191 | TTAATATCATAGCAG[A/C]GGTCTGAATACATAT | 94253 |
rs50165602 | snp | A/T | 0.18 | 0.24 | intron-variant | Hecw1 | Mm_Celera | 13:14370963 | GTACTTTCATGTTCT[A/T]CTTGCCTTTAACTTG | 94253 |
rs50168144 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Hecw1 | Mm_Celera | 13:14504370 | AATGGTGTGGAATGA[C/T]CCATGGGTAAGGTCA | 94253 |
rs50168407 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Hecw1 | Mm_Celera | 13:14344755 | CTAGAGAACTGACAC[A/G]GAGTCATAGAAATGA | 94253 |
rs50172624 | snp | A/C | 0.197531 | 0.244432 | intron-variant | Hecw1 | Mm_Celera | 13:14423437 | AAAAAACATGAGGAC[A/C]TTATAATAAGGAAGA | 94253 |
rs50179926 | snp | A/C | 0.391111 | 0.206368 | intron-variant | Hecw1 | Mm_Celera | 13:14250204 | ATACTTCATAGTCAC[A/C]AGATAATCAAATTTG | 94253 |
rs50204516 | snp | C/T | 0.124444 | 0.216185 | intron-variant, utr-variant-5-prime | Hecw1 | Mm_Celera | 13:14456064 | TCTTTTGTTGCCATT[C/T]TGTAATGTCCATATG | 94253 |
rs50206156 | snp | A/G | 0.297521 | 0.245442 | intron-variant | Hecw1 | Mm_Celera | 13:14374157 | TTGATGTTGTTCAAA[A/G]TAACAGTGGGAACTC | 94253 |
rs50217444 | snp | A/G | 0.35503 | 0.226867 | intron-variant | Hecw1 | Mm_Celera | 13:14251540 | GTTTGGAACAATATA[A/G]AGTCACTTGCAAAGA | 94253 |
rs50221591 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Hecw1 | Mm_Celera | 13:14308215 | TCTGTGCTCTACAGA[C/T]AGAAATGTGGTAGAA | 94253 |
rs50223986 | snp | C/G | 0.375 | 0.216506 | intron-variant | Hecw1 | Mm_Celera | 13:14414654 | TGAATAAAGAAATAG[C/G]AAGAAATGAGTAATG | 94253 |
rs50227902 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Hecw1 | Mm_Celera | 13:14467611 | CCAGTTTCCCTACAT[A/C]CAGGAGTCTCTTCAC | 94253 |
rs50228785 | snp | A/G | | | intron-variant | Hecw1 | Mm_Celera | 13:14433821 | GAGTTTGTCATTGGG[A/G]CCTTAGGAGAAGAGA | 94253 |
rs50234864 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Hecw1 | Mm_Celera | 13:14252081 | AGTTCCAATACACGC[C/T]CTCCAGCCCACACAA | 94253 |
rs50242820 | snp | C/T | 0.391111 | 0.206368 | intron-variant, utr-variant-5-prime | Hecw1 | Mm_Celera | 13:14455198 | AGTCATAATCAATAC[C/T]ACACTGAGACGGACA | 94253 |
rs50250259 | snp | C/G | 0.391111 | 0.206368 | intron-variant, utr-variant-5-prime | Hecw1 | Mm_Celera | 13:14455966 | ACATCTTGGCTAGCC[C/G]CTAGAGTGATTCTCC | 94253 |
rs50265129 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Hecw1 | Mm_Celera | 13:14359406 | GGCAGAGTAGTGGTT[A/T]TGTGAACCAAGAACT | 94253 |
rs50266439 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Hecw1 | Mm_Celera | 13:14259211 | CTCTCAACAGAAAAA[C/T]GTATACAGAAAATAC | 94253 |
rs50309701 | snp | C/T | | | intron-variant | Hecw1 | Mm_Celera | 13:14452132 | AGGATATCTACCTAT[C/T]CTAAGTCAGACAAGG | 94253 |
rs50311093 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Hecw1 | Mm_Celera | 13:14233058 | TCTGAGTAGTTCAAT[C/T]AGGATTAAGATTCTG | 94253 |
rs50315330 | snp | C/T | 0.473373 | 0.11227 | intron-variant | Hecw1 | Mm_Celera | 13:14413545 | ATTCTAGTATTTCAC[C/T]ATGCTATGTGCCAGG | 94253 |
rs50321315 | snp | A/C/G | 0.124444 | 0.216185 | intron-variant | Hecw1 | Mm_Celera | 13:14460106 | CCTCAAGCGAAGGTG[A/C/G]TGTTAGCCTATCAAC | 94253 |
rs50328394 | snp | A/C/T | 0.408163 | 0.193609 | intron-variant | Hecw1 | Mm_Celera | 13:14343090 | TTTGCATCATGGACA[A/C/T]CAAGAGATGAATTAA | 94253 |
rs50337190 | snp | A/G | 0.32 | 0.24 | intron-variant | Hecw1 | Mm_Celera | 13:14389233 | TAGGGATGGAACTCA[A/G]CTGAGAGTAGCACTA | 94253 |
rs50342210 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Hecw1 | Mm_Celera | 13:14231377 | TTCTGGTGGCTCATA[C/G]TTGCCAGAATCTGTC | 94253 |
rs50348228 | snp | C/T | 0.426035 | 0.177515 | intron-variant | Hecw1 | Mm_Celera | 13:14469206 | AATTTTTGATGAGCT[C/T]ACACTTGATTGTTCA | 94253 |
rs50356069 | snp | C/T | 0.124444 | 0.216185 | synonymous-codon | Hecw1 | Mm_Celera | 13:14234433 | TAATCGCAATCTCTG[C/T]TCATTATTGAAGCGT | 94253 |
rs50370352 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Hecw1 | Mm_Celera | 13:14425001 | TAGTGCTTACATGAA[A/G]CAGTTAGATAACATA | 94253 |
rs50371883 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Hecw1 | Mm_Celera | 13:14490530 | TTCCTTGAAGGCCCA[C/T]GCTGAATTTAATTGT | 94253 |
rs50372468 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Hecw1 | Mm_Celera | 13:14387229 | TAATGCAATATATGA[C/T]AATTCAACAGTGTTA | 94253 |
rs50379614 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Hecw1 | Mm_Celera | 13:14426412 | GAGCAGAGAAGTTGA[A/G]TTGGGTTTCCCTAAA | 94253 |
rs50387156 | snp | G/T | 0.408163 | 0.193609 | intron-variant | Hecw1 | Mm_Celera | 13:14369340 | TAAATTTGTGGGCGT[G/T]TTCTGACTATCAGGG | 94253 |
rs50391869 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Hecw1 | Mm_Celera | 13:14380017 | AGGAAATGGGCTGCA[C/T]ATAACTAAATTTGAA | 94253 |
rs50403477 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Hecw1 | Mm_Celera | 13:14278063 | TTCCTCCAAGTCAGT[G/T]GAAATAATTTTAACA | 94253 |
rs50403872 | snp | A/G | | | intron-variant | Hecw1 | Mm_Celera | 13:14452137 | ATCTACCTATTCTAA[A/G]TCAGACAAGGGATTC | 94253 |
rs50407511 | snp | A/G | | | intron-variant | Hecw1 | Mm_Celera | 13:14284227 | ACCAGTCACAATGGC[A/G]AAGATCAATAACTGA | 94253 |
rs50419400 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Hecw1 | Mm_Celera | 13:14427085 | GTGATATACAAATGT[A/G]AGCCATTGAGTGTTA | 94253 |
rs50420196 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Hecw1 | Mm_Celera | 13:14481189 | TAAGGAATTCGAAAG[A/G]AAAACCCCTTATAAG | 94253 |
rs50422108 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Hecw1 | Mm_Celera | 13:14389315 | AGTGCAGTTCTTTGC[A/T]GAAGGTTCAGCAGTC | 94253 |
rs50423277 | snp | C/T | 0.35503 | 0.226867 | intron-variant | Hecw1 | Mm_Celera | 13:14425193 | TAGTACAGTCCAGGC[C/T]TTTTGTAAAAACACT | 94253 |
rs50424292 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Hecw1 | Mm_Celera | 13:14252837 | GTGGAAGAATACTGC[C/T]TACTGAATTCCAGAT | 94253 |
rs50424908 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Hecw1 | Mm_Celera | 13:14431857 | TCTAAGTGTCTATTT[A/G]AACCTGTCAGTTATT | 94253 |
rs50430883 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Hecw1 | Mm_Celera | 13:14245513 | TATTTGAGAATATTT[C/T]AACTTCGTACTGGAC | 94253 |
rs50431115 | snp | A/T | | | intron-variant | Hecw1 | Mm_Celera | 13:14307931 | TTGGTCTTTTTAAAA[A/T]TTTTGGCCTTTTATC | 94253 |
rs50452472 | snp | A/T | 0.459184 | 0.136902 | intron-variant | Hecw1 | Mm_Celera | 13:14480344 | GTGTCCCACATCCTC[A/T]GTCCTAGATCCAAAA | 94253 |
rs50476679 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Hecw1 | Mm_Celera | 13:14313359 | ACACAGGTTTTGTGG[A/G]TAAGTGGCTATGGCA | 94253 |
rs50482468 | snp | A/T | | | intron-variant | Hecw1 | Mm_Celera | 13:14236382 | AGGCTTTTAAAAGCG[A/T]TAAATTGGGCTCTGG | 94253 |
rs50486032 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Hecw1 | Mm_Celera | 13:14434548 | AAAAAAACCCAGTGA[C/T]GTTACCCGCACAGAG | 94253 |
rs50493791 | snp | G/T | 0.391111 | 0.206368 | intron-variant | Hecw1 | Mm_Celera | 13:14340538 | GTGACAATGCCTTAG[G/T]TGATGCTGCCTGGGA | 94253 |
rs50494481 | snp | C/T | | | intron-variant | Hecw1 | Mm_Celera | 13:14247236 | TAGGGCCCAACCAAT[C/T]CACTCTTGTTAGCAA | 94253 |
rs50499132 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Hecw1 | Mm_Celera | 13:14472399 | ACTCATGCAACAATA[A/G]GCAGCATATGATTTC | 94253 |
rs50515641 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Hecw1 | Mm_Celera | 13:14346665 | TGTATGCTTTAAAAA[C/G]AAGGCACCTCAGCAT | 94253 |
rs50518412 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Hecw1 | Mm_Celera | 13:14270412 | ATAAGGGGTCAGAGA[A/G]TAGATATTGTAGGCT | 94253 |
rs50518801 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Hecw1 | Mm_Celera | 13:14252320 | GCCATGATGATAAAC[C/T]CTGCAGTTATTGATC | 94253 |
rs50534245 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Hecw1 | Mm_Celera | 13:14323263 | GTAGGAGTTGAGAGG[C/T]TTCAATATGCACTGT | 94253 |
rs50543037 | snp | C/T | 0.459184 | 0.136902 | intron-variant, upstream-variant-2KB | Hecw1 | Mm_Celera | 13:14458887 | CACAGGCCTTGCCTG[C/T]AACGTGAAGCTCACC | 94253 |
rs50556847 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Hecw1 | Mm_Celera | 13:14395371 | ATTTCAAATGACATA[A/G]CATGAAATACAACTG | 94253 |
rs50568389 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Hecw1 | Mm_Celera | 13:14364563 | TTAATCATGTAAATG[C/T]ACTGCTTGTACGTGC | 94253 |
rs50570706 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Hecw1 | Mm_Celera | 13:14247928 | TATTGACTCACAGGT[A/G]CCTAAAAAACAAACC | 94253 |
rs50574716 | snp | A/T | 0.391111 | 0.206368 | intron-variant | Hecw1 | Mm_Celera | 13:14319877 | TATTTGTTTTTAACA[A/T]AGTAACTGCCTGCTA | 94253 |
rs50574852 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Hecw1 | Mm_Celera | 13:14231172 | TACTCTGTTATCCTG[A/G]GATCCAGTTGTCCAT | 94253 |
rs50575847 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Hecw1 | Mm_Celera | 13:14480399 | CAGACTACATGTAAA[A/G]CAAAGCAGGAAGCTT | 94253 |
rs50580290 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Hecw1 | Mm_Celera | 13:14273409 | ATGTTATAACAACAT[A/G]ATCCTGAAGCCCAAT | 94253 |
rs50586989 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Hecw1 | Mm_Celera | 13:14388490 | AGGACATTTTTACAC[C/T]GTGCCCAGTTTTAGT | 94253 |
rs50596105 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Hecw1 | Mm_Celera | 13:14501870 | GCTGCAGAAAAGAAG[C/T]CCATTTCACATTATT | 94253 |
rs50600435 | snp | A/G | | | intron-variant | Hecw1 | GRCm38.p3 | 13:14240879 | AAAAAGACAGAATAA[A/G]AGACTGGATATGTAA | 94253 |
rs50609804 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Hecw1 | Mm_Celera | 13:14324973 | GAGTAGAAGATGCAC[A/G]TCCTTAGGAAGGCCT | 94253 |
rs50612432 | snp | A/G | 0.32 | 0.24 | intron-variant | Hecw1 | Mm_Celera | 13:14430446 | TACAATAAGAACAAA[A/G]AGGTTACTCAAGGAA | 94253 |
rs50621864 | snp | A/G | 0.32 | 0.24 | intron-variant | Hecw1 | Mm_Celera | 13:14234652 | TCAGGTTTTAAAACA[A/G]GCAAATTTAGAATAT | 94253 |
rs50637061 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Hecw1 | Mm_Celera | 13:14273423 | TGATCCTGAAGCCCA[A/G]TAGTGTGTAAATGAG | 94253 |
rs50638221 | snp | A/C | 0.32 | 0.24 | intron-variant | Hecw1 | Mm_Celera | 13:14479389 | GACAGAATGACTTAA[A/C]ATTTCTTGTTCCTCT | 94253 |
rs50650896 | snp | C/T | | | intron-variant | Hecw1 | GRCm38.p3 | 13:14318220 | CTGAGTTCTCAGTAA[C/T]GCAGTAACAGTAACT | 94253 |
rs50656308 | snp | A/G | 0.21875 | 0.248039 | intron-variant | Hecw1 | Mm_Celera | 13:14504388 | ATGGGTAAGGTCAGC[A/G]ACACTCCTTCAGTGA | 94253 |
rs50658803 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | Hecw1 | Mm_Celera | 13:14380563 | AATAGATTTTAAAGT[A/G]TTTCTCTTTTGTTCA | 94253 |
rs50662462 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Hecw1 | Mm_Celera | 13:14298392 | CTCAATTCCTTCTTT[C/T]CCAGTCACAATCTCT | 94253 |
rs50677949 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Hecw1 | Mm_Celera | 13:14236350 | AGAAACCATTTTGTA[C/T]TGAAGTAAGGCTTTG | 94253 |
rs50688512 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Hecw1 | Mm_Celera | 13:14414698 | GACAGTGTGTGTAGT[A/G]TGGTGAGGAAAGACA | 94253 |
rs50691270 | snp | A/G | | | intron-variant | Hecw1 | Mm_Celera | 13:14253763 | CCATCATATGTGGCT[A/G]GAGCCATGGGTCCCT | 94253 |
rs50693376 | snp | C/T | | | intron-variant | Hecw1 | GRCm38.p3 | 13:14245148 | AGGAGAATGCCAGGG[C/T]AGGAGGATGGGAGAG | 94253 |
rs50707842 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Hecw1 | Mm_Celera | 13:14491451 | ACATGAATATGTGCA[C/T]GTGTTTCAATATCAT | 94253 |
rs50728372 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Hecw1 | Mm_Celera | 13:14479233 | CCATAGTTTCTTGGA[A/G]CTCATCATATGAACC | 94253 |
rs50785129 | snp | A/G | | | intron-variant | Hecw1 | Mm_Celera | 13:14284226 | CCAATCAGAATGACT[A/G]AGATAAAAAAACTCA | 94253 |
rs50791909 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Hecw1 | Mm_Celera | 13:14257195 | CATCATGGTCAAGTA[A/G]GCTTCATCTCAGGGA | 94253 |
rs50800236 | snp | A/G | 0.46281 | 0.131194 | intron-variant | Hecw1 | Mm_Celera | 13:14300663 | AATTCTCGAACATAT[A/G]CATATACAGAATGAA | 94253 |
rs50806063 | snp | A/G | 0.396694 | 0.202437 | intron-variant | Hecw1 | Mm_Celera | 13:14468512 | TGATCTATCCTGTTA[A/G]CCATGGCTTACATAG | 94253 |
rs50812176 | snp | A/G | | | intron-variant | Hecw1 | Mm_Celera | 13:14247357 | TAGGAGTTAGGGTTT[A/G]GGAAGAGTTAAGGAT | 94253 |
rs50813198 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Hecw1 | Mm_Celera | 13:14426912 | CTTACATCTATGGGG[C/G]CAGTTCCGGCAGGAG | 94253 |
rs50821830 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Hecw1 | Mm_Celera | 13:14460159 | TAAGAGCTCACTTCA[C/T]CACAATTTCAGTGTG | 94253 |
rs50824374 | snp | C/T | 0.32 | 0.24 | intron-variant | Hecw1 | Mm_Celera | 13:14250559 | CTGAATACTCCAGGT[C/T]GCAAAGCAGCTGCTC | 94253 |
rs50833509 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Hecw1 | Mm_Celera | 13:14291072 | CCATTAAATTGGTTT[A/G]TAATAATTCAGTACC | 94253 |
rs50833999 | snp | C/T | | | intron-variant | Hecw1 | Mm_Celera | 13:14237601 | CTTCTCAAAGGACAG[C/T]CATGCAAGACTTGAT | 94253 |
rs50838902 | snp | C/T | 0.32 | 0.24 | intron-variant | Hecw1 | Mm_Celera | 13:14238370 | GCTATGGCTTTACAT[C/T]TTCTGTCAGATGTGC | 94253 |
rs50840030 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Hecw1 | Mm_Celera | 13:14424876 | AGAAAACATTTAGTT[C/T]TTGCTGACAAAGAGA | 94253 |
rs50841507 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Hecw1 | Mm_Celera | 13:14460400 | AGAGGATGAAGTATT[A/G]TAGAGAAAATGTCTT | 94253 |
rs50846083 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Hecw1 | Mm_Celera | 13:14314717 | TGTGAGGAAGCAGCA[C/G]GTGGACTTACCCCCA | 94253 |
rs50861630 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Hecw1 | Mm_Celera | 13:14387392 | AGCCATTCCACCCTC[C/T]AGCAAAGATTCCTGT | 94253 |
rs50864446 | snp | C/T | | | intron-variant | Hecw1 | Mm_Celera | 13:14289941 | CTGGTTCTGTTGATT[C/T]TTTGTATAGTTCTTT | 94253 |
rs50866342 | snp | C/G | | | intron-variant | Hecw1 | Mm_Celera | 13:14239754 | GAGCCCTGGATACCC[C/G]AACACACCAGAAAAG | 94253 |
rs50878827 | snp | G/T | 0.489796 | 0.070696 | intron-variant | Hecw1 | Mm_Celera | 13:14308112 | GTTGAAATCCATGAA[G/T]AAACCCTTGACACTG | 94253 |