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 |