SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs6181992 | snp | A/T | 0.304688 | 0.243945 | intron-variant | Hecw2 | Mm_Celera | 1:53868717 | ATGACGATTTCCTTA[A/T]GANTCCGAGGAGAAA | 329152 |
rs6182012 | snp | C/T | 0.5 | 0 | intron-variant | Hecw2 | Mm_Celera | 1:53868720 | ACGATTTCCTTANGA[C/T]TCCGAGGAGAAAGGA | 329152 |
rs6182708 | snp | C/T | 0.5 | 0 | intron-variant | Hecw2 | Mm_Celera | 1:54066337 | ggcaggtgaattcag[C/T]tcaccaaccaaaggc | 329152 |
rs6182819 | snp | A/G | 0.5 | 0 | intron-variant | Hecw2 | Mm_Celera | 1:54066395 | acaggactggagggt[A/G]gagacaggcagatcc | 329152 |
rs6183140 | snp | C/T | 0.49827 | 0.0293608 | intron-variant | Hecw2 | GRCm38.p3 | 1:53868949 | AAACGGTACAGATGC[C/T]CATGATAGGCTTTGT | 329152 |
rs6184001 | snp | A/G | 0.5 | 0 | intron-variant | Hecw2 | Mm_Celera | 1:54066601 | tttttttgttgtttt[A/G]gtttttttttttttt | 329152 |
rs6187190 | snp | A/C | 0.359862 | 0.224567 | intron-variant | Hecw2 | Mm_Celera | 1:54060553 | TTAAACCCATGTCTA[A/C]GTTTTCCAAACCCAT | 329152 |
rs6187747 | snp | A/T | 0.375 | 0.216506 | intron-variant | Hecw2 | Mm_Celera | 1:54060636 | CATTAGCATCTAAAC[A/T]GATTCCAATTTCATT | 329152 |
rs6188229 | snp | A/G | 0.359862 | 0.224567 | intron-variant | Hecw2 | Mm_Celera | 1:54060734 | TATAACTGTCATTGT[A/G]GAGGCCTTTACTGTC | 329152 |
rs6188762 | snp | C/G | 0.359862 | 0.224567 | intron-variant | Hecw2 | Mm_Celera | 1:54060855 | TAATAACCATGAAGA[C/G]TCTACCAAACCCTAA | 329152 |
rs6189197 | snp | A/T | 0.5 | 0 | intron-variant | Hecw2 | Mm_Celera | 1:54060910 | TGGGTGACTAAGCTT[A/T]GACATTCAGTCATCT | 329152 |
rs6195969 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Hecw2 | Mm_Celera | 1:53869036 | CTTAATAAGTGGCAC[G/T]GTGCTATGGGACTTT | 329152 |
rs6197054 | snp | A/G | 0.5 | 0 | intron-variant | Hecw2 | Mm_Celera | 1:53869202 | ggcagtggtggccac[A/G]cctttaatcccagca | 329152 |
rs6203033 | snp | C/G | 0.5 | 0 | intron-variant | Hecw2 | Mm_Celera | 1:53994627 | tgacaggaacttaag[C/G]agggcaggaacntgg | 329152 |
rs6203055 | snp | A/G | 0.5 | 0 | intron-variant | Hecw2 | Mm_Celera | 1:53994639 | aagnagggcaggaac[A/G]tggaggcaagagttg | 329152 |
rs6203092 | snp | A/G | 0.5 | 0 | intron-variant | Hecw2 | GRCm38.p3 | 1:53994663 | agagttgatgcaggg[A/G]ccatggagggtgctg | 329152 |
rs6203600 | snp | C/G | 0.5 | 0 | intron-variant | Hecw2 | Mm_Celera | 1:53994723 | taaaacccaggacca[C/G]cacgcagggattata | 329152 |
rs6204154 | snp | A/T | 0.5 | 0 | intron-variant | Hecw2 | GRCm38.p3 | 1:53994818 | atcttatggaggcat[A/T]ttctgaattgagatt | 329152 |
rs6205282 | snp | C/T | 0.5 | 0 | intron-variant | Hecw2 | GRCm38.p3 | 1:53995007 | TAAAATATAGCTCAA[C/T]TNGGCTAAAACAANA | 329152 |
rs6205283 | snp | A/C | 0.5 | 0 | intron-variant | Hecw2 | GRCm38.p3 | 1:53995009 | AAATATAGCTCAANT[A/C]GGCTAAAACAANAGC | 329152 |
rs6205310 | snp | C/T | 0.5 | 0 | intron-variant | Hecw2 | GRCm38.p3 | 1:53995021 | ANTNGGCTAAAACAA[C/T]AGCAATGGCCAGATC | 329152 |
rs6205364 | snp | G/T | 0.5 | 0 | intron-variant | Hecw2 | Mm_Celera | 1:53995059 | TTTTGTTTTCTTAAC[G/T]AGTTACTTCAGATTA | 329152 |
rs6248481 | snp | A/G | 0.5 | 0 | intron-variant | Hecw2 | Mm_Celera | 1:54115186 | cacatctgagtttag[A/G]tgtcaccctagaaag | 329152 |
rs6263382 | snp | A/C | 0.359862 | 0.224567 | intron-variant | Hecw2 | Mm_Celera | 1:54115715 | GTATCAACTTAAGGA[A/C]TGCTACTATCACCAG | 329152 |
rs6286542 | snp | C/T | 0.5 | 0 | intron-variant | Hecw2 | Mm_Celera | 1:54149880 | tctggggattacaag[C/T]tcacagtccaaacag | 329152 |
rs6286999 | snp | C/G | 0.5 | 0 | intron-variant | Hecw2 | Mm_Celera | 1:54149951 | cctttctccttaact[C/G]tntgcattccngtgt | 329152 |
rs6287001 | snp | A/T | 0.5 | 0 | intron-variant | Hecw2 | Mm_Celera | 1:54149953 | tttctccttaactnt[A/T]tgcattccngtgttt | 329152 |
rs6287017 | snp | G/T | 0.5 | 0 | intron-variant | Hecw2 | Mm_Celera | 1:54149962 | aactntntgcattcc[G/T]gtgtttcttcctacn | 329152 |
rs6287051 | snp | A/C/T | 0.5 | 0 | intron-variant | Hecw2 | Mm_Celera | 1:54149977 | ngtgtttcttcctac[A/C/T]atcctcnctctgagc | 329152 |
rs6287055 | snp | C/T | 0.5 | 0 | intron-variant | Hecw2 | Mm_Celera | 1:54149984 | cttcctacnatcctc[C/T]ctctgagcattttct | 329152 |
rs6287504 | snp | C/T | 0.5 | 0 | intron-variant | Hecw2 | Mm_Celera | 1:54150000 | ctctgagcattttct[C/T]tgaatggatttccct | 329152 |
rs6287557 | snp | A/T | 0.5 | 0 | intron-variant | Hecw2 | Mm_Celera | 1:54150032 | ttcaataactatcca[A/T]gttatcctggagnaa | 329152 |
rs6287579 | snp | A/G | 0.5 | 0 | intron-variant | Hecw2 | Mm_Celera | 1:54150045 | cangttatcctggag[A/G]aaggcacagcattca | 329152 |
rs6287628 | snp | A/T | 0.5 | 0 | intron-variant | Hecw2 | Mm_Celera | 1:54150072 | ttcattttaacttga[A/T]tacttctaggaagac | 329152 |
rs6287666 | snp | C/T | 0.5 | 0 | intron-variant | Hecw2 | Mm_Celera | 1:54150088 | tacttctaggaagac[C/T]gtgcctccaaataaa | 329152 |
rs6295895 | snp | A/C | 0.5 | 0 | intron-variant | Hecw2 | Mm_Celera | 1:54123743 | TCCTGTAATAAATTT[A/C]CTTAAGTAAAAATGA | 329152 |
rs6307292 | snp | C/G | 0.304688 | 0.243945 | intron-variant | Hecw2 | Mm_Celera | 1:53933559 | GCTATAATTCCAGCA[C/G]AGGGCTCTCCAAGGT | 329152 |
rs6323965 | snp | A/G | 0.5 | 0 | intron-variant | Hecw2 | Mm_Celera | 1:53934418 | CTCTCGGGAAGGAAT[A/G]GACTGGTCCACAAGA | 329152 |
rs6324449 | snp | C/G | 0.304688 | 0.243945 | intron-variant | Hecw2 | Mm_Celera | 1:53934486 | GGCTGGCTAATGACA[C/G]AGTCAGCAGTGGAAT | 329152 |
rs6324992 | snp | C/T | 0.304688 | 0.243945 | intron-variant | Hecw2 | Mm_Celera | 1:53934573 | CACTGCATGAGATCT[C/T]GATTGGTGGCTGCCC | 329152 |
rs6325545 | snp | C/T | 0.5 | 0 | intron-variant | Hecw2 | Mm_Celera | 1:53934669 | GGCTCCCAGTAGTTC[C/T]ATTNTGGATGCNTCA | 329152 |
rs6325562 | snp | A/T | 0.5 | 0 | intron-variant | Hecw2 | Mm_Celera | 1:53934673 | CCCAGTAGTTCNATT[A/T]TGGATGCNTCACTAT | 329152 |
rs6325579 | snp | G/T | 0.5 | 0 | intron-variant | Hecw2 | Mm_Celera | 1:53934681 | TTCNATTNTGGATGC[G/T]TCACTATTAAATGCA | 329152 |
rs6336416 | snp | G/T | 0.290657 | 0.246672 | intron-variant | Hecw2 | Mm_Celera | 1:53856327 | GGGTACTCTAGACAC[G/T]AAATAGGATACCTCC | 329152 |
rs6336988 | snp | C/G | 0.484429 | 0.0868505 | intron-variant | Hecw2 | GRCm38.p3 | 1:53856431 | TTATAAGAAGCCCTC[C/G]ATGAGTCATCTATAT | 329152 |
rs6337597 | snp | A/G | 0.5 | 0 | intron-variant | Hecw2 | Mm_Celera | 1:53856526 | TCTGGAGGCTTGTCT[A/G]GGGAGATATAAACCT | 329152 |
rs6338179 | snp | A/G | 0.5 | 0 | intron-variant | Hecw2 | Mm_Celera | 1:53856635 | Gcagtggctctcaac[A/G]ttgagcacatatcag | 329152 |
rs6338206 | snp | C/T | 0.5 | 0 | intron-variant | Hecw2 | Mm_Celera | 1:53856655 | gcacatatcagaatc[C/T]cataggaactttaaa | 329152 |
rs6338652 | snp | G/T | 0.5 | 0 | intron-variant | Hecw2 | Mm_Celera | 1:53856675 | ggaactttaaaaaat[G/T]ccaaagcccagtcca | 329152 |
rs6338779 | snp | C/T | 0.5 | 0 | intron-variant | Hecw2 | Mm_Celera | 1:53856758 | gttttctacagctgt[C/T]caggtgagtccaaaa | 329152 |
rs6371761 | snp | C/T | 0.5 | 0 | intron-variant | Hecw2 | Mm_Celera | 1:54095234 | AGTAGTTAAAGGTAA[C/T]CCAAGAAAGTCTAGC | 329152 |
rs6372274 | snp | C/T | 0.5 | 0 | intron-variant | Hecw2 | Mm_Celera | 1:54095352 | GTTTCCTAACCTTTA[C/T]GTTGGCTTGTGGGGC | 329152 |
rs6386920 | snp | A/C/T | 0.494922 | 0.202172 | intron-variant | Hecw2 | GRCm38.p3 | 1:54095723 | TAAAGGCTAGGACAC[A/C/T]GCATCCGAGAGAACG | 329152 |
rs6389572 | snp | A/G | 0.5 | 0 | intron-variant | Hecw2 | Mm_Celera | 1:54168221 | GACTACAAGGCTGGC[A/G]GCTGTAGTCNCCCTA | 329152 |
rs6389589 | snp | A/G | 0.429688 | 0.173817 | intron-variant | Hecw2 | Mm_Celera | 1:54168231 | CTGGCNGCTGTAGTC[A/G]CCCTAACCCTGTCTT | 329152 |
rs6389621 | snp | C/T | 0.429688 | 0.173817 | intron-variant | Hecw2 | Mm_Celera | 1:54168262 | ACCAAGTTTCAAGAT[C/T]ACCTCAACCTAACCC | 329152 |
rs6406541 | snp | A/G | 0.489796 | 0.070696 | intron-variant | Hecw2 | Mm_Celera | 1:54024190 | AAGCAGTTAACCACT[A/G]AAACAAAACTCTTCT | 329152 |
rs6406690 | snp | C/T | 0.5 | 0 | intron-variant | Hecw2 | GRCm38.p3 | 1:54024268 | ATTCATCTAGAGGAG[C/T]TTAGGGAGNGAGGGA | 329152 |
rs6407117 | snp | A/G | 0.5 | 0 | intron-variant | Hecw2 | GRCm38.p3 | 1:54024277 | GAGGAGNTTAGGGAG[A/G]GAGGGATATCTACAA | 329152 |
rs6408803 | snp | A/G | 0.5 | 0 | intron-variant | Hecw2 | Mm_Celera | 1:54024606 | aagtactcatatggt[A/G]actcacaaccatcag | 329152 |
rs29552601 | snp | A/T | 0.5 | 0 | intron-variant | Hecw2 | Mm_Celera | 1:53920125 | AAGGGAGCAAAAACC[A/T]TTCAGTGGAAAAAGG | 329152 |
rs30458955 | snp | A/T | 0.375 | 0.216506 | intron-variant | Hecw2 | Mm_Celera | 1:54075696 | TATTCTTGGCTATTC[A/T]TGGCTGTCAACTACA | 329152 |
rs30464765 | snp | A/G | 0.375 | 0.216506 | intron-variant | Hecw2 | Mm_Celera | 1:54184262 | CAAATGTGGTGGAAA[A/G]GCTGTGGATGTGTGG | 329152 |
rs30476938 | snp | A/G | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54133594 | TGCTCCTTCATTCCT[A/G]CCACATGGACTAAGG | 329152 |
rs30496792 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Hecw2 | Mm_Celera | 1:54120540 | AGCTCACAACCACCT[A/G]GACCTCCAACCCCAG | 329152 |
rs30506354 | snp | C/T | 0.375 | 0.216506 | intron-variant | Hecw2 | Mm_Celera | 1:54111300 | AACTGCCTACTCTAC[C/T]TTTACTTACAAAATA | 329152 |
rs30507791 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Hecw2 | Mm_Celera | 1:54105059 | ATAAACACACCACTG[A/T]GTGTTGACAACTCAC | 329152 |
rs30508615 | snp | C/T | 0.375 | 0.216506 | intron-variant | Hecw2 | Mm_Celera | 1:54187940 | TTCCAGCTGAGTTTC[C/T]AAGTGTCTCTTCAAT | 329152 |
rs30517470 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Hecw2 | Mm_Celera | 1:54161814 | TTTGATTATCTTATG[A/G]ATCAGCATCACCTGA | 329152 |
rs30518194 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Hecw2 | Mm_Celera | 1:54178762 | TTAAATGTCTACAGG[A/C]CCCAAGAAGTTCTGC | 329152 |
rs30521120 | snp | A/G | 0.375 | 0.216506 | intron-variant | Hecw2 | Mm_Celera | 1:54175742 | AATAGGACAAGTGAG[A/G]TAATATCTAATGTCT | 329152 |
rs30525025 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Hecw2 | Mm_Celera | 1:54183485 | TTAACATTCTGTACC[A/G]ATTTAATATCTGATT | 329152 |
rs30573767 | snp | A/G | 0.487535 | 0.077957 | intron-variant | Hecw2 | Mm_Celera | 1:54162763 | ACGAACTTCAGAAAT[A/G]AAATGGCAGCTTGTG | 329152 |
rs30596250 | snp | C/T | 0.375 | 0.216506 | intron-variant | Hecw2 | Mm_Celera | 1:54101273 | TAAGGTATGTCAGAC[C/T]GTAATTCTTACAAAC | 329152 |
rs30598652 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Hecw2 | Mm_Celera | 1:54087059 | ATTGGATACTAGATC[C/T]ACACCAGGCCAGCAG | 329152 |
rs30602485 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Hecw2 | Mm_Celera | 1:54182163 | ACTCCTAGAATGAAG[G/T]TTTTACTCCTACTTT | 329152 |
rs30612203 | snp | A/T | 0.375 | 0.216506 | intron-variant | Hecw2 | Mm_Celera | 1:54075697 | ATTCTTGGCTATTCT[A/T]GGCTGTCAACTACAT | 329152 |
rs30689709 | snp | C/T | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54084551 | TTTCCATTAAAGACT[C/T]GTTGTCTAATTAAAT | 329152 |
rs30702290 | snp | G/T | 0.42 | 0.183303 | intron-variant | Hecw2 | Mm_Celera | 1:54091250 | TGCAAGCACTCTTCC[G/T]AGCATGAGTCAGGCC | 329152 |
rs30731025 | snp | C/T | 0.375 | 0.216506 | upstream-variant-2KB | Hecw2 | GRCm38.p3 | 1:54196327 | ATAGCAACCCTCTAT[C/T]TGTTTTTATACTCTT | 329152 |
rs30764783 | snp | G/T | 0.465374 | 0.126941 | intron-variant | Hecw2 | Mm_Celera | 1:54160662 | CTGAGGGTGATGCTG[G/T]GCTAACAGGAGGAGT | 329152 |
rs30801997 | snp | A/G | 0.290657 | 0.246672 | intron-variant | Hecw2 | Mm_Celera | 1:54107428 | CTTCAGGAATTCTCA[A/G]TTAAGTGAGGAAGAC | 329152 |
rs30858737 | snp | C/T | 0.345679 | 0.230967 | intron-variant | Hecw2 | Mm_Celera | 1:54127590 | TTTTTCCCTTCTGGT[C/T]CTGGCATGACTCTTA | 329152 |
rs30864847 | snp | A/G | 0.375 | 0.216506 | intron-variant | Hecw2 | Mm_Celera | 1:54101986 | AGGGCTCTCTGAGCT[A/G]CCAGTCTAGTCTAAT | 329152 |
rs30893340 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Hecw2 | Mm_Celera | 1:54186112 | TCTTTTATCACCACA[A/G]TCTGCAAGTTATGCA | 329152 |
rs30895908 | snp | C/T | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54110222 | ACCTCTACAGATGAG[C/T]TATGGCATGTTTGGA | 329152 |
rs30915980 | snp | C/T | 0.375 | 0.216506 | intron-variant | Hecw2 | Mm_Celera | 1:54165841 | TCACAGCAATAGTAA[C/T]CCTAACTAAGACAGT | 329152 |
rs30916566 | snp | A/G | 0.32 | 0.24 | intron-variant | Hecw2 | GRCm38.p3 | 1:54155688 | TGTCTTACAGAGATT[A/G]CAATTCAGTGTATGA | 329152 |
rs30989983 | snp | C/T | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54167376 | TTCGAGACAGGGTTT[C/T]TCTGTATAGCCCTGG | 329152 |
rs31010809 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Hecw2 | Mm_Celera | 1:54183921 | TTTTTCAATTGTCTA[G/T]CAAAAGACAGTTGGA | 329152 |
rs31029571 | snp | A/G | 0.475309 | 0.108333 | intron-variant | Hecw2 | Mm_Celera | 1:54159344 | TCCCATTTGAAAGCC[A/G]GTCTTTTAACTCTCT | 329152 |
rs31040575 | snp | A/T | 0.375 | 0.216506 | intron-variant | Hecw2 | Mm_Celera | 1:54177437 | ACATGGACTATTTTT[A/T]AAAATTGAGACTGGG | 329152 |
rs31055451 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Hecw2 | Mm_Celera | 1:54127734 | GGATCGTAATGTAAA[C/T]ATCTGATATGCAGGA | 329152 |
rs31086025 | snp | A/G | 0.375 | 0.216506 | intron-variant | Hecw2 | Mm_Celera | 1:54117480 | AAGGAGGGCACAAGG[A/G]AGGATGCTTGAATCT | 329152 |
rs31087875 | snp | C/G | 0.415225 | 0.187619 | intron-variant | Hecw2 | Mm_Celera | 1:54118895 | GCCCCCAGCCTTCTG[C/G]TCTTGTATCTCTGCC | 329152 |
rs31158149 | snp | C/T | 0.5 | 0 | intron-variant | Hecw2 | Mm_Celera | 1:54180533 | TGAACAATGACTGTG[C/T]TGACAAGCATGACCA | 329152 |
rs31186167 | snp | A/G | 0.375 | 0.216506 | intron-variant | Hecw2 | Mm_Celera | 1:54187146 | CCCCATCCCTTCCAC[A/G]GTGCATCGTAAGTTC | 329152 |
rs31234094 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Hecw2 | Mm_Celera | 1:53869244 | GAGGCAGGCAGATTT[C/T]TGAGTTTGAGGCCAG | 329152 |
rs31249365 | snp | A/G | 0.375 | 0.216506 | intron-variant | Hecw2 | Mm_Celera | 1:54107153 | TGGGCAATGGTAGTA[A/G]TTTATGCTGTTTGAG | 329152 |
rs31302932 | snp | C/T | 0.375 | 0.216506 | intron-variant | Hecw2 | Mm_Celera | 1:54173992 | GGAGAAAGCAAAGAG[C/T]TCACAAAGCACTATG | 329152 |