SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs3673155 | snp | A/C | 0.5 | 0 | intron-variant | Nedd4l | Mm_Celera | 18:65144530 | GTTCCGTCCCCCCCC[A/C]CACACACACACACCC | 83814 |
rs3701978 | snp | C/G | 0.5 | 0 | intron-variant | Nedd4l | Mm_Celera | 18:64952095 | atctggcttacactt[C/G]tacactgtatgtcca | 83814 |
rs3703036 | snp | A/C | 0.359862 | 0.224567 | intron-variant | Nedd4l | GRCm38.p3 | 18:65187453 | TGTGGATCTCCTCTT[A/C]GATGCAGGATCATCC | 83814 |
rs3703744 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Nedd4l | GRCm38.p3 | 18:64919336 | TCTGCTCGGCCTTTA[A/G]ACATTGGGAAGCTCA | 83814 |
rs3704805 | snp | C/G | 0.5 | 0 | intron-variant | Nedd4l | GRCm38.p3 | 18:65187713 | GCCTGTTACAGCTTA[C/G]GTCTGTCCATGAGAC | 83814 |
rs4231907 | snp | C/T | 0.476371 | 0.106096 | intron-variant | Nedd4l | GRCm38.p3 | 18:64982296 | AACCACGATTAAACA[C/T]TCATATACTATTTTT | 83814 |
rs6168396 | snp | A/G | 0.484429 | 0.0868505 | intron-variant | Nedd4l | Mm_Celera | 18:65107683 | CCTACACTAACTTCA[A/G]TCAAATGCGGTTAGA | 83814 |
rs6168967 | snp | A/G | 0.484429 | 0.0868505 | intron-variant | Nedd4l | Mm_Celera | 18:65107768 | TGTGGCAGACCTAGC[A/G]ATGTAAAACTCATAG | 83814 |
rs6169026 | snp | A/G | 0.207612 | 0.24638 | intron-variant | Nedd4l | Mm_Celera | 18:65107816 | GGCTGTGTAGACACC[A/G]TGGACCATCTGGCTT | 83814 |
rs6170088 | snp | G/T | 0.5 | 0 | intron-variant | Nedd4l | Mm_Celera | 18:65107955 | GTCTTCACTGCCTCA[G/T]ACAGTGTCTGGTCCT | 83814 |
rs6182634 | snp | A/G/T | 0.304498 | 0.276817 | intron-variant, upstream-variant-2KB | Nedd4l | GRCm38.p3 | 18:65141755 | CTAAACTTTATTCAA[A/G/T]CTCACAANTCATGAG | 83814 |
rs6182649 | snp | G/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | Nedd4l | Mm_Celera | 18:65141763 | TATTCAANCTCACAA[G/T]TCATGAGTTGTCTCT | 83814 |
rs6182674 | snp | C/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | Nedd4l | Mm_Celera | 18:65141785 | GTTGTCTCTTAGATA[C/T]CCCTGTCCCCTGATG | 83814 |
rs6183873 | snp | A/G | 0.5 | 0 | intron-variant, upstream-variant-2KB | Nedd4l | Mm_Celera | 18:65141991 | GTAGAGGACAGATGA[A/G]CCTGCTCCAGAGTTC | 83814 |
rs6184423 | snp | A/C | 0.5 | 0 | intron-variant, upstream-variant-2KB | Nedd4l | Mm_Celera | 18:65142076 | TAGGCAGAAGTACTG[A/C]CATNATTTTTCAGGC | 83814 |
rs6184435 | snp | C/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | Nedd4l | Mm_Celera | 18:65142080 | CAGAAGTACTGNCAT[C/T]ATTTTTCAGGCCTTC | 83814 |
rs6191280 | snp | G/T | 0.5 | 0 | intron-variant | Nedd4l | Mm_Celera | 18:65003497 | ATCTTGCAGAGGGAT[G/T]AATTCACCCATACTA | 83814 |
rs6197348 | snp | C/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | Nedd4l | Mm_Celera | 18:65142221 | CAAATTCCTCAAAAG[C/T]ATTTGTAgctggggt | 83814 |
rs6214744 | snp | C/G | 0.304688 | 0.243945 | intron-variant | Nedd4l | Mm_Celera | 18:64927019 | CTTCCTCTCTTGATC[C/G]TCAGACAGCTTGGGA | 83814 |
rs6228968 | snp | G/T | 0.5 | 0 | intron-variant | Nedd4l | Mm_Celera | 18:64927233 | CCCACCCCAGGAGTT[G/T]NGTGGAGGAACCCTT | 83814 |
rs6228969 | snp | A/C | 0.5 | 0 | intron-variant | Nedd4l | GRCm38.p3 | 18:64927234 | CCACCCCAGGAGTTN[A/C]GTGGAGGAACCCTTG | 83814 |
rs6229003 | snp | C/T | 0.493827 | 0.0552116 | intron-variant | Nedd4l | GRCm38.p3 | 18:64927250 | GTGGAGGAACCCTTG[C/T]CTGCTGGGGACTTCA | 83814 |
rs6229648 | snp | G/T | 0.426035 | 0.177515 | intron-variant | Nedd4l | Mm_Celera | 18:64927401 | TTGTGTGGTCATGAA[G/T]TTTAGGTTATAGGTT | 83814 |
rs6233209 | snp | A/G | 0.5 | 0 | intron-variant | Nedd4l | Mm_Celera | 18:65150789 | CTGGAACCTTCTCCC[A/G]CCTCTTCCCTTCTAT | 83814 |
rs6284201 | snp | A/C | 0.5 | 0 | intron-variant | Nedd4l | GRCm38.p3 | 18:64903793 | ACCAAGAACCCCCTC[A/C]CCCCTTCTATTGCGT | 83814 |
rs6285204 | snp | C/T | 0.5 | 0 | intron-variant | Nedd4l | Mm_Celera | 18:64903968 | GGGTCTTTGTGAAAA[C/T]GTAAACCAAATCTAA | 83814 |
rs6285225 | snp | A/G | 0.426035 | 0.177515 | intron-variant | Nedd4l | Mm_Celera | 18:64903987 | AACCAAATCTAATAG[A/G]GTGAGCCTCCTAGGT | 83814 |
rs6298507 | snp | C/T | 0.35503 | 0.226867 | intron-variant | Nedd4l | Mm_Celera | 18:64904016 | GTACTCCTCTTACAC[C/T]TTCCTTGCCTTccat | 83814 |
rs6298573 | snp | C/T | 0.5 | 0 | intron-variant | Nedd4l | Mm_Celera | 18:64904058 | tcaccatcatgacca[C/T]catcatcatccttgt | 83814 |
rs6299131 | snp | C/T | 0.5 | 0 | intron-variant | Nedd4l | Mm_Celera | 18:64904152 | TCCCATCCTTCCCTC[C/T]GCCTCACAGCCNTGG | 83814 |
rs6299160 | snp | A/G | 0.5 | 0 | intron-variant | Nedd4l | Mm_Celera | 18:64904164 | CTCNGCCTCACAGCC[A/G]TGGAAGGCTCANGCA | 83814 |
rs6299183 | snp | C/T | 0.5 | 0 | intron-variant | Nedd4l | Mm_Celera | 18:64904176 | GCCNTGGAAGGCTCA[C/T]GCAGGGTTACGGAGT | 83814 |
rs6306707 | snp | A/G | 0.5 | 0 | intron-variant | Nedd4l | Mm_Celera | 18:65121491 | CGTGGCCTGCCTGCC[A/G]GCAAGGAGGCTGAAA | 83814 |
rs6306802 | snp | C/T | 0.290657 | 0.246672 | intron-variant | Nedd4l | Mm_Celera | 18:65121553 | TGGGCAGAATTTGTA[C/T]ATTAAAGTCTACTGG | 83814 |
rs6319139 | snp | G/T | 0.5 | 0 | intron-variant | Nedd4l | Mm_Celera | 18:65167289 | AACATTAGTCACCCC[G/T]ATCAAGGATGTAGTC | 83814 |
rs6319592 | snp | A/G | 0.459184 | 0.136902 | intron-variant | Nedd4l | Mm_Celera | 18:65167368 | GCCCAGCTTCATTTG[A/G]ACAAGGCGGATAGCN | 83814 |
rs6319608 | snp | A/G | 0.5 | 0 | intron-variant | Nedd4l | Mm_Celera | 18:65167383 | NACAAGGCGGATAGC[A/G]GGGATACCAATCTCA | 83814 |
rs6320743 | snp | C/T | 0.459184 | 0.136902 | missense, intron-variant, nc-transcript-variant | Nedd4l | Mm_Celera | 18:65167568 | ACGGGTGGTGAGGAA[C/T]CCACGGTAATGACCC | 83814 |
rs6321776 | snp | C/T | 0.32 | 0.24 | intron-variant | Nedd4l | Mm_Celera | 18:65167707 | GAGACACCTGCACTT[C/T]TTANCCTAAACTTCT | 83814 |
rs6321790 | snp | A/G/T | 0.426035 | 0.177515 | intron-variant | Nedd4l | GRCm38.p3 | 18:65167711 | CACCTGCACTTNTTA[A/G/T]CCTAAACTTCTCATT | 83814 |
rs6322407 | snp | A/G | 0.304688 | 0.243945 | intron-variant | Nedd4l | Mm_Celera | 18:65167834 | TGGACTGTTTTGGTC[A/G]GTGTCTGTACTCCGG | 83814 |
rs6323096 | snp | A/T | 0.5 | 0 | intron-variant | Nedd4l | Mm_Celera | 18:64899716 | ATTTCTTGGCAACTC[A/T]TGACAGNCTTACTCC | 83814 |
rs6323101 | snp | A/G | 0.5 | 0 | intron-variant | Nedd4l | Mm_Celera | 18:64899723 | GGCAACTCNTGACAG[A/G]CTTACTCCTTATGAC | 83814 |
rs6323143 | snp | A/G | 0.5 | 0 | intron-variant | Nedd4l | Mm_Celera | 18:64899746 | CTTATGACCTATATC[A/G]GTAAAGACAGAACAG | 83814 |
rs6323231 | snp | A/G | 0.5 | 0 | intron-variant | Nedd4l | Mm_Celera | 18:64899796 | TGAAGAGAAGGATGA[A/G]AAAACANGCGTGGAG | 83814 |
rs6323233 | snp | C/T | 0.5 | 0 | intron-variant | Nedd4l | Mm_Celera | 18:64899803 | AAGGATGANAAAACA[C/T]GCGTGGAGTGGTTGG | 83814 |
rs6324292 | snp | A/G | 0.5 | 0 | intron-variant | Nedd4l | Mm_Celera | 18:64899949 | GGGTGGACATTGTCA[A/G]AGTTCCTCTCCTTGA | 83814 |
rs6338547 | snp | G/T | 0.5 | 0 | intron-variant | Nedd4l | Mm_Celera | 18:64900204 | CTGTCTTGAAACAAC[G/T]TTCAGANTGGACTGC | 83814 |
rs6338554 | snp | C/T | 0.5 | 0 | intron-variant | Nedd4l | Mm_Celera | 18:64900211 | GAAACAACNTTCAGA[C/T]TGGACTGCTACGGGG | 83814 |
rs6356598 | snp | A/G | 0.359862 | 0.224567 | intron-variant | Nedd4l | Mm_Celera | 18:65103530 | CTAGATTTGAGAGCC[A/G]TTGACCTGTCCNCCA | 83814 |
rs6356610 | snp | C/T | 0.5 | 0 | intron-variant | Nedd4l | Mm_Celera | 18:65103542 | GCCNTTGACCTGTCC[C/T]CCATGTNTTGCTGGC | 83814 |
rs6356624 | snp | A/G | 0.304688 | 0.243945 | intron-variant | Nedd4l | Mm_Celera | 18:65103549 | ACCTGTCCNCCATGT[A/G]TTGCTGGCTCTAAAC | 83814 |
rs6356690 | snp | A/G | 0.5 | 0 | intron-variant | Nedd4l | Mm_Celera | 18:65103588 | ATTCATTTTCTATTT[A/G]TAAAACGGCAATCCT | 83814 |
rs6357151 | snp | A/G | 0.359862 | 0.224567 | intron-variant | Nedd4l | Mm_Celera | 18:65103696 | GACTACAGGATTAGG[A/G]AAACACTTGCTGTGG | 83814 |
rs6380720 | snp | C/T | 0.5 | 0 | intron-variant | Nedd4l | Mm_Celera | 18:65099100 | ggctcttatgtagcc[C/T]aggttgatcttggaa | 83814 |
rs6380869 | snp | C/T | 0.5 | 0 | intron-variant | Nedd4l | Mm_Celera | 18:65099196 | tgggggtcagcccca[C/T]ggcttcatcatgctg | 83814 |
rs6381314 | snp | C/T | 0.255 | 0.24995 | intron-variant | Nedd4l | Mm_Celera | 18:65099248 | GCTACATCCTCAGCA[C/T]ACAACTCATACTAAG | 83814 |
rs6381812 | snp | A/G | 0.5 | 0 | intron-variant | Nedd4l | Mm_Celera | 18:65099322 | GAACAGCATCAGGGG[A/G]TGGGATCCCGCCTCC | 83814 |
rs6381890 | snp | A/C | 0.290657 | 0.246672 | intron-variant | Nedd4l | Mm_Celera | 18:65099380 | TTGGTAAACAGCAGC[A/C]TGAAAGTGTAACTGA | 83814 |
rs6394947 | snp | A/G | 0.290657 | 0.246672 | intron-variant | Nedd4l | Mm_Celera | 18:65099400 | AGTGTAACTGATGGA[A/G]GGGTTTCCCCAGTCG | 83814 |
rs13459225 | snp | A/C | | | missense, nc-transcript-variant | Nedd4l | Mm_Celera | 18:65172384 | ACAATCGAACCACAA[A/C]TTGGACTCGGCCAAT | 83814 |
rs13483405 | snp | A/G | 0.473373 | 0.11227 | intron-variant | Nedd4l | GRCm38.p3 | 18:65087273 | TATCCTGAGATGGTT[A/G]GGCTGTCTTTACTCA | 83814 |
rs29536614 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Nedd4l | Mm_Celera | 18:65036592 | GAATTTGAAAGATAG[A/C]ATATCTTTCATAGAT | 83814 |
rs29537609 | snp | A/C | 0.33241 | 0.236027 | intron-variant | Nedd4l | GRCm38.p3 | 18:65101953 | CCAGACAGAGTGTGT[A/C]AATGTGATCGATCAC | 83814 |
rs29539595 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Nedd4l | GRCm38.p3 | 18:65083928 | CCGCAGCTCCTGGCC[C/G]GGGTGGACGCCAGGC | 83814 |
rs29540134 | snp | C/G | 0.5 | 0 | intron-variant | Nedd4l | Mm_Celera | 18:65072896 | TCCCAGACCAGAGAC[C/G]GCCAAGGGGAAGGTC | 83814 |
rs29540267 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Nedd4l | GRCm38.p3 | 18:65100276 | CAGACAACCAAAGAG[A/G]CTAGAAGATGGCAAC | 83814 |
rs29540468 | snp | C/T | 0.493827 | 0.0552116 | intron-variant | Nedd4l | Mm_Celera | 18:65197818 | CATATAATTTTCGGT[C/T]TCCTTTGAGCCTGTC | 83814 |
rs29540587 | snp | C/T | 0.465374 | 0.126941 | intron-variant | Nedd4l | Mm_Celera | 18:65071160 | CCAGCTAAGTACATT[C/T]ATGGTTATCTCCTGA | 83814 |
rs29542524 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Nedd4l | GRCm38.p3 | 18:65060500 | AATGTAATAAAACTC[C/T]GAGAAGCCACCTTCC | 83814 |
rs29543238 | snp | A/G | 0.5 | 0 | intron-variant | Nedd4l | GRCm38.p3 | 18:64918682 | GTGCTTCCTATGTCC[A/G]TCATCTTGACTTGTA | 83814 |
rs29543762 | snp | A/G | 0.5 | 0 | intron-variant | Nedd4l | GRCm38.p3 | 18:65060384 | GATAGTGAGATTTGT[A/G]TGGAAAATCAATTCT | 83814 |
rs29544598 | snp | C/G | 0.33241 | 0.236027 | intron-variant | Nedd4l | GRCm38.p3 | 18:65194872 | CTGCTCCAGTGAACC[C/G]TAACTGTCAATTACA | 83814 |
rs29546996 | snp | A/C | 0.429688 | 0.173817 | intron-variant | Nedd4l | GRCm38.p3 | 18:65098600 | GACAAGAATTCCTCA[A/C]GGGTGTTTGAGGACT | 83814 |
rs29547480 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Nedd4l | Mm_Celera | 18:65070217 | ACATTGTGCTTGTAA[A/G]CAAATGGCTTTGAGC | 83814 |
rs29547560 | snp | C/T | 0.5 | 0 | intron-variant | Nedd4l | GRCm38.p3 | 18:65109445 | CTGATGCTGCACAAC[C/T]AACTTCATGACTAAC | 83814 |
rs29550058 | snp | C/T | 0.432133 | 0.171253 | intron-variant | Nedd4l | Mm_Celera | 18:65095291 | TCGTCAGTTCATCTT[C/T]TGGCCTGTCATGCAT | 83814 |
rs29551483 | snp | A/G | 0.375 | 0.216506 | intron-variant | Nedd4l | GRCm38.p3 | 18:65035917 | GCCATCCGTGGGCTG[A/G]TGGTCCTAGGATCTA | 83814 |
rs29551834 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Nedd4l | GRCm38.p3 | 18:65131698 | GGCAGTGGCTTTCTT[C/T]CTTTTCTCTTGCTTT | 83814 |
rs29551937 | snp | C/T | 0.42 | 0.183303 | intron-variant | Nedd4l | GRCm38.p3 | 18:65096119 | ATGGTGTTTAAATGG[C/T]TCAGCACAGAAGGAG | 83814 |
rs29552791 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Nedd4l | Mm_Celera | 18:65064651 | AGGAATTGTTAGGAG[C/T]CTAGCCTGGGCTTCT | 83814 |
rs29552838 | snp | A/C | 0.484429 | 0.0868505 | intron-variant | Nedd4l | Mm_Celera | 18:65031195 | AAATCCCATAACATT[A/C]GAAAAATAACTACTG | 83814 |
rs29553388 | snp | A/G | 0.387812 | 0.208586 | intron-variant | Nedd4l | Mm_Celera | 18:65077916 | TGAAGATCTGTGGAG[A/G]TTTCATTTGGAGCTA | 83814 |
rs29553689 | snp | A/G | 0.5 | 0 | intron-variant | Nedd4l | Mm_Celera | 18:65189541 | GTCTATGTACTAGCA[A/G]GTGTTGAAAGTCATA | 83814 |
rs29553758 | snp | A/G | 0.375 | 0.216506 | intron-variant | Nedd4l | GRCm38.p3 | 18:65036064 | TGCTTTTCTTAATGA[A/G]CTGTTATGTGGAACT | 83814 |
rs29554700 | snp | A/G | 0.375 | 0.216506 | upstream-variant-2KB, nc-transcript-variant | Nedd4l, A330084C13Rik | GRCm38.p3 | 18:64886075 | ACTTCCCTTCCCCCA[A/G]CTGCCCTTCCCTACA | 83814 |
rs29555038 | snp | G/T | 0.375 | 0.216506 | intron-variant | Nedd4l | GRCm38.p3 | 18:65037757 | AGCTGAGGAGCTGTT[G/T]GTGGTTGGTGGCTGC | 83814 |
rs29555997 | snp | A/G | 0.489796 | 0.070696 | intron-variant | Nedd4l | Mm_Celera | 18:65030056 | ATCCTCCAGCCTGCT[A/G]TCTGTGTACTGCCCA | 83814 |
rs29556122 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Nedd4l | Mm_Celera | 18:64937318 | GGATTTTGCCCTATG[A/G]CCACTAATGTTTCCC | 83814 |
rs29556169 | snp | A/G | 0.32 | 0.24 | intron-variant | Nedd4l | GRCm38.p3 | 18:65134081 | TGAAAATTCTCCTCC[A/G]AACACTGTGTGTAAA | 83814 |
rs29556847 | snp | C/T | 0.475309 | 0.108333 | intron-variant | Nedd4l | Mm_Celera | 18:65177892 | GCTGCTTGTACCCTT[C/T]TCTGTTCTTGCTATT | 83814 |
rs29556854 | snp | A/G | 0.375 | 0.216506 | intron-variant | Nedd4l | Mm_Celera | 18:65096694 | GGCAAGAGAGGCCAG[A/G]TTATGCAACCCCAAA | 83814 |
rs29556883 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Nedd4l | Mm_Celera | 18:65092080 | TTCTACAGGAAGACC[A/G]GTCTAACAACTGTTA | 83814 |
rs29556958 | snp | A/G | 0.387812 | 0.208586 | intron-variant | Nedd4l | Mm_Celera | 18:65098367 | TGCGTGCTGCCTGCC[A/G]TCTTCTGCCTTCCAT | 83814 |
rs29557439 | snp | C/T | 0.188366 | 0.242283 | intron-variant | Nedd4l | Mm_Celera | 18:65174965 | GTCCCTAACTCTGTA[C/T]GTAAGCTGAATTTCT | 83814 |
rs29557515 | snp | C/G | 0.49827 | 0.0293608 | intron-variant | Nedd4l | GRCm38.p3 | 18:65135008 | CAGACCCAGGACTAT[C/G]CTCATGGCAAATATA | 83814 |
rs29557641 | snp | G/T | 0.387812 | 0.208586 | intron-variant | Nedd4l | Mm_Celera | 18:65085051 | CACACTCTTTTTAGA[G/T]TTCCTTCTGGATGAA | 83814 |
rs29558012 | snp | G/T | 0.487535 | 0.077957 | intron-variant | Nedd4l | GRCm38.p3 | 18:65002018 | TAATTGAATCCTTTA[G/T]AGAGTGGGATGCCAG | 83814 |
rs29558320 | snp | G/T | 0.484429 | 0.0868505 | intron-variant | Nedd4l | GRCm38.p3 | 18:65005295 | GGCTAAGAATCCTAA[G/T]ACTGTAATGCCATGT | 83814 |
rs29558486 | snp | C/T | 0.492188 | 0.0620098 | intron-variant | Nedd4l | Mm_Celera | 18:65068951 | TTACGTGATTTGTTA[C/T]AAAAAACTTCAGTCA | 83814 |
rs29558489 | snp | C/T | 0.492188 | 0.0620098 | intron-variant | Nedd4l | Mm_Celera | 18:65162952 | GGTAGACAGGTAATT[C/T]CCCAGATCCTAGCAC | 83814 |
rs29558641 | snp | A/G | 0.375 | 0.216506 | intron-variant | Nedd4l | GRCm38.p3 | 18:65005991 | ATCCCATTACAGATG[A/G]TTGTGAGCTACCATG | 83814 |
rs29559081 | snp | C/T | 0.375 | 0.216506 | intron-variant | Nedd4l | Mm_Celera | 18:65002202 | GTGTGTGCGCGCGTG[C/T]GTGTGTGTGTGTGTG | 83814 |
rs29559475 | snp | C/T | 0.415225 | 0.187619 | intron-variant | Nedd4l | GRCm38.p3 | 18:65004750 | ATCTGGAAGTTTTCC[C/T]TTTAAACTTGGAATA | 83814 |
rs29559653 | snp | C/G | 0.475309 | 0.108333 | intron-variant, upstream-variant-2KB | Nedd4l | GRCm38.p3 | 18:65024043 | GTGCAGAACGGTCTC[C/G]TGTTGTGGATCTGTG | 83814 |
rs29559753 | snp | A/T | 0.375 | 0.216506 | intron-variant | Nedd4l | GRCm38.p3 | 18:64985298 | GTATACATTCCAACC[A/T]GAACCCCAGACCTCA | 83814 |
rs29559881 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Nedd4l | GRCm38.p3 | 18:65146343 | TGAAAGTTCCACCGC[C/T]TTCCTCCAGGATGCC | 83814 |
rs29560241 | snp | A/G/T | 0.444444 | 0.157135 | intron-variant | Nedd4l | GRCm38.p3 | 18:64941392 | CTGCCTCTGCCTCCC[A/G/T]AGTGCTGGGATTAAA | 83814 |
rs29560539 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Nedd4l | GRCm38.p3 | 18:64905396 | TCGTGCTCACTGTTG[A/G]TTTGATTTTGCCTAA | 83814 |
rs29560687 | snp | A/G | 0.493827 | 0.0552116 | intron-variant | Nedd4l | Mm_Celera | 18:65031043 | AGTAAATGCTAAAAT[A/G]ACTATGGCTGATAAA | 83814 |
rs29560724 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Nedd4l | GRCm38.p3 | 18:64966816 | TACAGGGAGCCCTCC[A/G]TTTGATCCCCAGCAC | 83814 |
rs29560937 | snp | G/T | 0.375 | 0.216506 | intron-variant | Nedd4l | GRCm38.p3 | 18:65010169 | GTGCAAGCAGATGCA[G/T]ATGTATAGCCGACTG | 83814 |
rs29562372 | snp | C/T | 0.475309 | 0.108333 | intron-variant | Nedd4l | GRCm38.p3 | 18:65058014 | AAAATGCCTAATGTG[C/T]GGTAAGAACCAGTAC | 83814 |
rs29562495 | snp | A/G | 0.375 | 0.216506 | intron-variant | Nedd4l | GRCm38.p3 | 18:64969787 | GCTTATAAGACCAGA[A/G]GATTAAGTCCATAAT | 83814 |
rs29563117 | snp | G/T | 0.5 | 0 | intron-variant | Nedd4l | Mm_Celera | 18:65196840 | TATGTGTGCGTGTAT[G/T]TATGTGTGTATGTTT | 83814 |
rs29571523 | snp | A/G | 0.5 | 0 | intron-variant | Nedd4l | Mm_Celera | 18:65063861 | AGAAGTGCATCCTAT[A/G]AGGTGTTCTGAATTG | 83814 |
rs29571818 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Nedd4l | GRCm38.p3 | 18:65123804 | TCTTCATTGAACCTG[G/T]AGCTTTACCATTGCA | 83814 |
rs29573487 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Nedd4l | Mm_Celera | 18:65066774 | AGAAGAGGGCATCCA[A/G]TCCTCTGGAACTGGA | 83814 |
rs29573837 | snp | C/T | 0.375 | 0.216506 | intron-variant | Nedd4l | GRCm38.p3 | 18:65030399 | TCCTTGTTACCCTTT[C/T]CTCATAACTCCAGAA | 83814 |
rs29573952 | snp | C/T | 0.5 | 0 | intron-variant | Nedd4l | GRCm38.p3 | 18:65158444 | GTATCGCTGCCTTGG[C/T]ATATTTAGAAACGCA | 83814 |
rs29574346 | snp | A/G | 0.32 | 0.24 | intron-variant | Nedd4l | Mm_Celera | 18:64963569 | GTGGCAATAAGATAT[A/G]TATTATTTATATGTT | 83814 |
rs29574866 | snp | G/T | 0.493827 | 0.0552116 | intron-variant | Nedd4l | GRCm38.p3 | 18:65133730 | TCTGGCCCCAGATCA[G/T]TAGCAGCAAGTGAGG | 83814 |
rs29574913 | snp | A/C | 0.475309 | 0.108333 | intron-variant | Nedd4l | Mm_Celera | 18:64987019 | CAACAGTTTTTAGTC[A/C]ACTTGAGTTTCAGTT | 83814 |
rs29574950 | snp | C/T | 0.46875 | 0.121031 | intron-variant | Nedd4l | GRCm38.p3 | 18:64970863 | AGGCAAATTCCACTA[C/T]GAATTACATGTCTCG | 83814 |
rs29575173 | snp | A/G | 0.493827 | 0.0552116 | intron-variant | Nedd4l | GRCm38.p3 | 18:65132529 | GCTAGGAGTTACAGA[A/G]AGATGGGATCATAGT | 83814 |
rs29575276 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Nedd4l | Mm_Celera | 18:65097019 | AGTGGTGCTTGGGGG[C/T]GTGCTCCGCAAAATT | 83814 |
rs29575502 | snp | C/T | 0.489796 | 0.070696 | intron-variant | Nedd4l | Mm_Celera | 18:65072431 | GGCTTAGCTACTCTT[C/T]GAAGTTAGTTACATA | 83814 |
rs29575739 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Nedd4l | GRCm38.p3 | 18:65070509 | GTAGCGAGGACTCAC[A/G]TATTCCAGGCTGACC | 83814 |
rs29575892 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Nedd4l | GRCm38.p3 | 18:65211409 | CACCCACCGTCTCAT[C/T]CTTTAAATGCTCTTG | 83814 |
rs29575896 | snp | G/T | 0.455 | 0.143091 | intron-variant | Nedd4l | GRCm38.p3 | 18:64918738 | TTCTTTGGGTTCTAT[G/T]GAATGCCTGCTACCT | 83814 |
rs29576067 | snp | A/T | 0.345679 | 0.230967 | intron-variant | Nedd4l | GRCm38.p3 | 18:65081933 | GAATGCAGAGCGATT[A/T]AAAAACCCGATGAGC | 83814 |
rs29576188 | snp | G/T | 0.375 | 0.216506 | intron-variant | Nedd4l | GRCm38.p3 | 18:65002074 | ATCTGCAGGGGCCGG[G/T]TGAAGCCTGGCTGCT | 83814 |
rs29577033 | snp | A/G | 0.387812 | 0.208586 | intron-variant | Nedd4l | Mm_Celera | 18:65097263 | GATGCCTTTTCTCCC[A/G]GTAGCTGCATTTTCT | 83814 |
rs29577461 | snp | C/G | 0.493827 | 0.0552116 | intron-variant | Nedd4l | Mm_Celera | 18:65170373 | TAGATGACAGAACAT[C/G]AGACTAGGCTTCCAG | 83814 |
rs29577819 | snp | C/G | 0.375 | 0.216506 | intron-variant | Nedd4l | Mm_Celera | 18:64979716 | TGTTTGTTTTTGTGG[C/G]TATTTTGTGAAAGAT | 83814 |
rs29577874 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Nedd4l | Mm_Celera | 18:65092113 | TTAGTGCTGGGGAAG[G/T]GCTTAGGCTCCCTGG | 83814 |
rs29578233 | snp | G/T | 0.459184 | 0.136902 | intron-variant | Nedd4l | Mm_Celera | 18:65184045 | TGGCATGCAAAGGAG[G/T]CTGGCTGGCTGGCAT | 83814 |
rs29578451 | snp | A/T | 0.498615 | 0.0262793 | intron-variant | Nedd4l | Mm_Celera | 18:65124234 | TTTGTCATTCTCCCG[A/T]GTCCATGTTGTTAAA | 83814 |
rs29578700 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Nedd4l | GRCm38.p3 | 18:64966854 | AAGTTGATGTGCCAG[C/T]ACACACCTATAATAC | 83814 |
rs29578820 | snp | C/T | 0.415225 | 0.187619 | intron-variant | Nedd4l | Mm_Celera | 18:65068976 | CAGTCAGTATCTTTG[C/T]ATGCGTTTGTACATT | 83814 |
rs29578892 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Nedd4l | GRCm38.p3 | 18:64988090 | CTTATAACACTGTGG[C/T]TGCTTCTGTCCCCTT | 83814 |
rs29578901 | snp | A/G | 0.5 | 0 | intron-variant | Nedd4l | Mm_Celera | 18:65182284 | GAGACTCCTGTCCCC[A/G]AGCAGTGCTCACACA | 83814 |
rs29579107 | snp | C/T | 0.375 | 0.216506 | intron-variant | Nedd4l | Mm_Celera | 18:65078590 | CTGCTATTAAACACC[C/T]CCAAACTGCTCCAGC | 83814 |
rs29579596 | snp | C/T | 0.207612 | 0.24638 | intron-variant | Nedd4l | GRCm38.p3 | 18:65126955 | TGTTACATTAGGACC[C/T]GAATCTTTGCAGGCT | 83814 |
rs29580107 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Nedd4l | Mm_Celera | 18:65098033 | GGCAAACACACACAC[A/G]CGCGCGCGCGCGCAC | 83814 |
rs29580388 | snp | G/T | 0.375 | 0.216506 | intron-variant | Nedd4l | Mm_Celera | 18:65001117 | CCACTGTGTGCTTCA[G/T]AACCCTGGGCCAGCA | 83814 |
rs29580437 | snp | C/T | 0.415225 | 0.187619 | intron-variant | Nedd4l | GRCm38.p3 | 18:65060374 | GCAAGTTAAAGATAG[C/T]GAGATTTGTATGGAA | 83814 |
rs29580593 | snp | A/T | 0.48 | 0.0979796 | utr-variant-3-prime, nc-transcript-variant | Nedd4l | GRCm38.p3 | 18:65214020 | TCCGGTGCGGTATCT[A/T]TCAGGTGTGAACTTG | 83814 |
rs29580768 | snp | C/T | 0.375 | 0.216506 | intron-variant | Nedd4l | GRCm38.p3 | 18:64941149 | ATAAATATGGTACCA[C/T]TGGGGCTGGGGGTGT | 83814 |
rs29581739 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Nedd4l | GRCm38.p3 | 18:64937755 | CAGGTAAGATGCCTG[A/G]TCATGATGACGCCAT | 83814 |
rs29582274 | snp | C/T | 0.475309 | 0.108333 | intron-variant | Nedd4l | GRCm38.p3 | 18:65198101 | TGTGGCCACAAACAA[C/T]GCGTAGCCAGGCTAT | 83814 |
rs29582483 | snp | G/T | 0.375 | 0.216506 | intron-variant | Nedd4l | Mm_Celera | 18:64916520 | GGGAGAAATATTTTT[G/T]TTAGGAACTTGCATC | 83814 |
rs29588104 | snp | A/G | 0.465374 | 0.126941 | intron-variant | Nedd4l | Mm_Celera | 18:65194417 | GGAGGATCTCTGCAC[A/G]CCCCTTACCACTGGG | 83814 |
rs29618109 | snp | C/G | 0.5 | 0 | intron-variant | Nedd4l | GRCm38.p3 | 18:64985798 | TGGGGTGTATTCTGA[C/G]CACATACCATGTATT | 83814 |
rs29621080 | snp | G/T | 0.375 | 0.216506 | intron-variant | Nedd4l | Mm_Celera | 18:65110834 | GGTTAGTCCATGGTA[G/T]CCATGGTGGGGAGAC | 83814 |
rs29622649 | snp | C/T | 0.5 | 0 | intron-variant | Nedd4l | Mm_Celera | 18:65110528 | GTGCCTGCATGCTGC[C/T]ATGCTCCTGCCTTGA | 83814 |
rs29622650 | snp | A/G | 0.375 | 0.216506 | intron-variant | Nedd4l | Mm_Celera | 18:65179356 | GGAAACTGTGGAAGG[A/G]AAAGGCACAAATAAT | 83814 |
rs29622887 | snp | A/C | 0.46875 | 0.121031 | intron-variant | Nedd4l | GRCm38.p3 | 18:65150933 | ATGTCTCCATCTCAG[A/C]CACGGTTGTATCCGT | 83814 |
rs29622893 | snp | A/T | 0.33241 | 0.236027 | intron-variant | Nedd4l | GRCm38.p3 | 18:65193494 | GGCGAAGCACTGTAC[A/T]CTGTGAACGCCTGAA | 83814 |
rs29623111 | snp | A/G | 0.5 | 0 | intron-variant, upstream-variant-2KB, nc-transcript-variant | Nedd4l, A330084C13Rik | GRCm38.p3 | 18:64888274 | GCTCTCGGGGTGGGC[A/G]GAGGCCGCGTGCGCC | 83814 |
rs29624006 | snp | G/T | 0.5 | 0 | intron-variant | Nedd4l | GRCm38.p3 | 18:64932317 | GACAGAGTGAAGACT[G/T]TGTGTGGAGACTTCT | 83814 |
rs29624012 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Nedd4l | GRCm38.p3 | 18:64983273 | TATCTTAGGCAGTTT[A/G]TAGATCCACTGTAAA | 83814 |
rs29624317 | snp | A/G | 0.375 | 0.216506 | intron-variant | Nedd4l | GRCm38.p3 | 18:65001134 | ACCCTGGGCCAGCAA[A/G]CAATTTCCCTTCACC | 83814 |
rs29624410 | snp | C/T | 0.493827 | 0.0552116 | intron-variant | Nedd4l | GRCm38.p3 | 18:64977807 | CTGTGTAGTGAGAAC[C/T]GAAGTATTTCTGTGG | 83814 |
rs29624595 | snp | A/G | 0.375 | 0.216506 | intron-variant | Nedd4l | Mm_Celera | 18:64891599 | TATTCCGGTGGGTGA[A/G]TGGGCCTGTTGGACC | 83814 |
rs29625115 | snp | A/G | 0.375 | 0.216506 | intron-variant | Nedd4l | Mm_Celera | 18:64956234 | AAGAAAGCAGGCTGA[A/G]CAAGCCAGGGGAAGC | 83814 |
rs29625643 | snp | A/C | 0.5 | 0 | intron-variant | Nedd4l | GRCm38.p3 | 18:65211284 | ACTCAGTTGGGCTCC[A/C]GTGTTTCTGCACAGG | 83814 |
rs29625674 | snp | A/G | 0.415225 | 0.187619 | intron-variant | Nedd4l | Mm_Celera | 18:65134419 | TTCAGAAAGTACCCA[A/G]TATGACAGGTAGGCT | 83814 |
rs29626047 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Nedd4l | Mm_Celera | 18:65197160 | ATGCCCATGATGCCA[A/G]CTAGAGCTCACTGTG | 83814 |
rs29626707 | snp | A/G | 0.475309 | 0.108333 | intron-variant | Nedd4l | GRCm38.p3 | 18:65097537 | GGGCCCCTGATGCCC[A/G]AACTACCCTCTTCCT | 83814 |
rs29627210 | snp | C/T | 0.459184 | 0.136902 | intron-variant | Nedd4l | GRCm38.p3 | 18:65029162 | ACCACCATTGGTAGT[C/T]GTCCTTCATGGGAAG | 83814 |
rs29627652 | snp | A/G | 0.375 | 0.216506 | intron-variant | Nedd4l | GRCm38.p3 | 18:65035890 | GGGAGGGACCAGACC[A/G]TTGTGGGTAGTGCCA | 83814 |
rs29627790 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Nedd4l | GRCm38.p3 | 18:65206584 | AAAGCAGCCCGAAGG[A/G]CTGGTGAGACGGCTC | 83814 |
rs29628442 | snp | C/T | 0.387812 | 0.208586 | intron-variant | Nedd4l | GRCm38.p3 | 18:65094799 | GCAGGCTATTGTAAG[C/T]TCATATCTCCTTCAA | 83814 |
rs29628603 | snp | A/G | 0.35503 | 0.226867 | intron-variant | Nedd4l | Mm_Celera | 18:65123396 | TTTTTAAACAACTTT[A/G]GTTTACTGGGAGCTC | 83814 |
rs29628767 | snp | C/T | 0.375 | 0.216506 | intron-variant | Nedd4l | Mm_Celera | 18:65096439 | TCCAAACACTGCAGA[C/T]GGAATTCATAGAGTT | 83814 |
rs29629117 | snp | A/G | 0.345679 | 0.230967 | intron-variant | Nedd4l | GRCm38.p3 | 18:65088898 | TGATCTGGGGGTGCT[A/G]CTGCTCTGCTTGGGG | 83814 |
rs29629670 | snp | G/T | 0.345679 | 0.230967 | intron-variant | Nedd4l | Mm_Celera | 18:65197475 | CTCAAGTGTTGGGAC[G/T]CTAGGTGTTCAACAC | 83814 |
rs29630560 | snp | A/C | 0.456747 | 0.140554 | intron-variant | Nedd4l | GRCm38.p3 | 18:64968259 | AGAATTTAAGTTCTC[A/C]TCTCCTTAATAATCA | 83814 |
rs29630827 | snp | C/G | 0.375 | 0.216506 | intron-variant | Nedd4l | GRCm38.p3 | 18:65035909 | TGGGTAGTGCCATCC[C/G]TGGGCTGATGGTCCT | 83814 |
rs29631547 | snp | A/G | 0.5 | 0 | intron-variant | Nedd4l | GRCm38.p3 | 18:65211219 | AGGACAGGGACAGAC[A/G]CCGCTTAGGAGATTT | 83814 |
rs29631700 | snp | C/T | 0.489796 | 0.070696 | intron-variant | Nedd4l | Mm_Celera | 18:65167253 | TAAGAATCTGCTAAG[C/T]TTTGGACTGTGGAAG | 83814 |
rs29633659 | snp | A/G | 0.375 | 0.216506 | intron-variant | Nedd4l | GRCm38.p3 | 18:65055104 | TTCTGCCTGCTCCAC[A/G]GCCTCCTGGAGTTGC | 83814 |
rs29634469 | snp | C/T | 0.498615 | 0.0262793 | intron-variant | Nedd4l | Mm_Celera | 18:65091611 | GTGGAGTGGGTCATT[C/T]GGTAGGGTGTGTATA | 83814 |
rs29668663 | snp | A/G | 0.5 | 0 | intron-variant | Nedd4l | Mm_Celera | 18:65151296 | TAAGGCTGGGCCTTT[A/G]GCAACTTTCTCCTAC | 83814 |
rs29671380 | snp | C/G | 0.456747 | 0.140554 | intron-variant | Nedd4l | GRCm38.p3 | 18:65033170 | TTCCTTCGCTCTGTG[C/G]CCATGTCCCAGGATC | 83814 |
rs29671640 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Nedd4l | GRCm38.p3 | 18:65004953 | CTGGGATTTCATGTT[C/T]CCTTACTGAAAGTGA | 83814 |
rs29672266 | snp | C/T | 0.387812 | 0.208586 | intron-variant | Nedd4l | GRCm38.p3 | 18:65107224 | TTTGCAATTAGGTAA[C/T]GTGTCTCATATAGAA | 83814 |
rs29672779 | snp | C/T | 0.415225 | 0.187619 | synonymous-codon, nc-transcript-variant | Nedd4l | GRCm38.p3 | 18:65186330 | AATGTTTTCAGATAG[C/T]AAAATTACCCAGTGG | 83814 |
rs29673095 | snp | A/G | 0.5 | 0 | intron-variant | Nedd4l | GRCm38.p3 | 18:64937587 | TTCTAGGATAGGGGA[A/G]GTAACGTCCAGCAGG | 83814 |
rs29674675 | snp | C/T | 0.375 | 0.216506 | intron-variant | Nedd4l | GRCm38.p3 | 18:64921691 | TCACACTTCTGGGAG[C/T]TAGGACCCCCAATAT | 83814 |
rs29674775 | snp | C/T | 0.5 | 0 | intron-variant | Nedd4l | GRCm38.p3 | 18:65210694 | GCGAAGCTTAAGCCA[C/T]GACTTGGATGGGTCC | 83814 |
rs29674780 | snp | A/G | 0.401235 | 0.199068 | intron-variant | Nedd4l | Mm_Celera | 18:65080299 | AAAGTCACCTATGAC[A/G]ACCTCACCCCAGATG | 83814 |
rs29675111 | snp | A/G | 0.375 | 0.216506 | intron-variant | Nedd4l | Mm_Celera | 18:65158878 | AACCCAAGGCAAAAA[A/G]AAAAGATCTCCCAGT | 83814 |
rs29676188 | snp | A/G | 0.429688 | 0.173817 | intron-variant | Nedd4l | GRCm38.p3 | 18:65186303 | GATTAGAACTAACTC[A/G]TTGGTGTTTTTAATG | 83814 |
rs29676704 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Nedd4l | Mm_Celera | 18:65088020 | TAAAGGCAGTACATG[A/G]GGCTGATACTGGCTA | 83814 |
rs29676708 | snp | A/G | 0.32 | 0.24 | intron-variant | Nedd4l | GRCm38.p3 | 18:65106150 | ACTGCCTGTGGCCTA[A/G]GGAGCACCAGTTAGG | 83814 |
rs29676781 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Nedd4l | Mm_Celera | 18:65197888 | GACCTGATAGCCTCA[C/T]GGCTACTCTCTTCTA | 83814 |
rs29676899 | snp | C/T | 0.375 | 0.216506 | intron-variant | Nedd4l | Mm_Celera | 18:65168438 | ACTAGGCTGCTAAGC[C/T]GCTACAGTCAAGAAC | 83814 |
rs29677338 | snp | A/G | 0.304688 | 0.243945 | intron-variant | Nedd4l | Mm_Celera | 18:64923511 | GGCATGCCTTGGGAG[A/G]TAGTTTTGTCCCTTC | 83814 |
rs29678379 | snp | G/T | 0.489796 | 0.070696 | intron-variant | Nedd4l | Mm_Celera | 18:65031072 | AAAACATTGCACAAA[G/T]TCTTTTTACTTTTTA | 83814 |
rs29678498 | snp | A/G | 0.49827 | 0.0293608 | intron-variant | Nedd4l | Mm_Celera | 18:65064885 | CTTTTTTGTATCTCC[A/G]AGTGGATCATTTCTG | 83814 |
rs29680398 | snp | C/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | Nedd4l, A330084C13Rik | GRCm38.p3 | 18:64889669 | GAGATTCTGACGTTC[C/T]TAAACAAAGGGCTTC | 83814 |
rs29719376 | snp | C/T | 0.375 | 0.216506 | intron-variant | Nedd4l | GRCm38.p3 | 18:65056821 | TGAAGATGGTGATGT[C/T]TGGCTATTTGAGTCA | 83814 |
rs29719550 | snp | C/T | 0.375 | 0.216506 | upstream-variant-2KB, nc-transcript-variant | Nedd4l, A330084C13Rik | GRCm38.p3 | 18:64886172 | TGCTCTCCTCTCTCT[C/T]TCTTCCCCTCTCTCA | 83814 |
rs29719680 | snp | C/G | 0.5 | 0 | intron-variant | Nedd4l | Mm_Celera | 18:65063485 | TACATTGATTTCTCT[C/G]TGTGTGTGTGTGTGT | 83814 |
rs29719857 | snp | C/T | 0.498615 | 0.0262793 | intron-variant | Nedd4l | Mm_Celera | 18:65183274 | CCTGCACCCTGCCCA[C/T]AGTTACCTAATGTAG | 83814 |
rs29720232 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Nedd4l | GRCm38.p3 | 18:64971454 | AAGGAAGTCAGGACA[C/T]GGACTCACACAGGAC | 83814 |
rs29721061 | snp | C/T | 0.375 | 0.216506 | intron-variant | Nedd4l | GRCm38.p3 | 18:65059117 | CACCTAGCCCAGCCT[C/T]GATGACCTTGAATTT | 83814 |
rs29721095 | snp | C/T | 0.493827 | 0.0552116 | intron-variant | Nedd4l | Mm_Celera | 18:64987002 | CAGTCTCACTCTTCC[C/T]TCAACAGTTTTTAGT | 83814 |
rs29721113 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Nedd4l | GRCm38.p3 | 18:64923883 | AAGAAGTTACTGGTG[C/G]AAGGTGGTATGGCAT | 83814 |
rs29722319 | snp | A/G | 0.5 | 0 | intron-variant | Nedd4l | GRCm38.p3 | 18:65210693 | AGCGAAGCTTAAGCC[A/G]TGACTTGGATGGGTC | 83814 |
rs29722348 | snp | C/T | 0.459184 | 0.136902 | intron-variant | Nedd4l | GRCm38.p3 | 18:64981308 | GATGAGAGGCAACCA[C/T]CCTACATTCCCCAGG | 83814 |
rs29722436 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Nedd4l | Mm_Celera | 18:65167193 | CTGTGCTGCGCTCAT[G/T]GACCCCCCCCCCCCC | 83814 |
rs29723021 | snp | G/T | 0.375 | 0.216506 | intron-variant | Nedd4l | GRCm38.p3 | 18:65094885 | CCCAGTTACTCCCCA[G/T]AGTGCCAAGGATAAT | 83814 |
rs29723022 | snp | A/G | 0.32 | 0.24 | intron-variant, upstream-variant-2KB | Nedd4l, A330084C13Rik | GRCm38.p3 | 18:64890199 | TACCAATAGAAAAAT[A/G]AATGCCTCCATATTT | 83814 |
rs29723126 | snp | G/T | 0.375 | 0.216506 | intron-variant | Nedd4l | GRCm38.p3 | 18:64918558 | TGGCTGCTTGGCCAG[G/T]GGATGATGGGATTCC | 83814 |
rs29723183 | snp | C/T | 0.375 | 0.216506 | intron-variant | Nedd4l | GRCm38.p3 | 18:65188097 | GAATCGATCTTCCTC[C/T]AGGTCCACCTCTAAC | 83814 |
rs29723423 | snp | G/T | 0.375 | 0.216506 | intron-variant | Nedd4l | Mm_Celera | 18:65111580 | CCAGTGAACTTCTGA[G/T]TTCCACCCATCTCTT | 83814 |
rs29723517 | snp | A/T | 0.484429 | 0.0868505 | intron-variant | Nedd4l | Mm_Celera | 18:65036711 | AGAAATTACCAGACG[A/T]AGGTGAAAGTTAAAA | 83814 |
rs29723522 | snp | A/G | 0.5 | 0 | intron-variant | Nedd4l | GRCm38.p3 | 18:65210821 | ACTGTCTATGAGTAC[A/G]ACAGTCCCCGGCCTC | 83814 |
rs29724400 | snp | A/C | 0.456747 | 0.140554 | intron-variant | Nedd4l | GRCm38.p3 | 18:65057402 | TCAATGCTGCACTGA[A/C]GGTGAGCTGTCTATA | 83814 |
rs29724586 | snp | A/G | 0.5 | 0 | intron-variant | Nedd4l | GRCm38.p3 | 18:65110556 | TGATGATAATGGACT[A/G]AACCTCTGAACCTGT | 83814 |
rs29725696 | snp | A/G | 0.475309 | 0.108333 | intron-variant | Nedd4l | Mm_Celera | 18:65072861 | CCTGAACAATGACCA[A/G]AAAGGCCAACTCTGT | 83814 |
rs29727094 | snp | A/T | 0.32 | 0.24 | intron-variant | Nedd4l | Mm_Celera | 18:64979941 | CTCTTTCAGTTGTTT[A/T]GTTACTAAGACTTAA | 83814 |
rs29727795 | snp | A/G | 0.375 | 0.216506 | intron-variant | Nedd4l | Mm_Celera | 18:65030089 | CTTTGCCTGGAAAGG[A/G]CCCCTTCTCTGAGGG | 83814 |
rs29727841 | snp | C/T | 0.456747 | 0.140554 | intron-variant | Nedd4l | GRCm38.p3 | 18:64983150 | CTGTCCTGCCTTTTC[C/T]TCTGAGGTGGGCAGT | 83814 |
rs29727869 | snp | C/T | 0.432133 | 0.171253 | intron-variant | Nedd4l | GRCm38.p3 | 18:65117138 | AAAAGCCACTGGGTT[C/T]GCTGATGCATATTGG | 83814 |
rs29728556 | snp | A/G | 0.387812 | 0.208586 | intron-variant | Nedd4l | GRCm38.p3 | 18:65095319 | CATTTTTCCCTGATC[A/G]GCTGGGGACTTGAGG | 83814 |
rs29728676 | snp | G/T | 0.375 | 0.216506 | intron-variant | Nedd4l | Mm_Celera | 18:64986403 | TTTGTTTGTTTGTTT[G/T]TGTTTTTTCCCCCCT | 83814 |
rs29730070 | snp | A/G | 0.375 | 0.216506 | intron-variant | Nedd4l | GRCm38.p3 | 18:65194405 | AGCTTGTGTGCTGGA[A/G]GATCTCTGCACACCC | 83814 |
rs29731039 | snp | A/G | 0.432133 | 0.171253 | intron-variant | Nedd4l | GRCm38.p3 | 18:64986131 | CACCTGTGCTGTGGT[A/G]CCGTATGTGATCATA | 83814 |
rs29736305 | snp | G/T | 0.495 | 0.0497494 | intron-variant | Nedd4l | Mm_Celera | 18:65064723 | CTCTGATGGGAGGTC[G/T]CGTGTGATACCTACC | 83814 |
rs29764893 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Nedd4l | GRCm38.p3 | 18:65070185 | TGAAATGTCTTCTTT[A/G]GTACACAGATGTGTG | 83814 |
rs29765960 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Nedd4l | Mm_Celera | 18:64899543 | ACACACACACAAAGA[A/G]AGAGAGAGAGAGAGA | 83814 |
rs29766228 | snp | G/T | 0.32 | 0.24 | intron-variant, upstream-variant-2KB | Nedd4l | GRCm38.p3 | 18:65022794 | CCTAGACAAGGTTGA[G/T]TCTGAGGGGTCATGG | 83814 |
rs29766305 | snp | G/T | 0.456747 | 0.140554 | intron-variant | Nedd4l | Mm_Celera | 18:64893763 | CTGTTACTGGGAAAC[G/T]GGTATCAGAAAGTTG | 83814 |
rs29767408 | snp | C/T | 0.345679 | 0.230967 | intron-variant | Nedd4l | GRCm38.p3 | 18:65127974 | TGCTTGCTTGACCTT[C/T]CTTCATGAATGTCAT | 83814 |
rs29767905 | snp | A/C | 0.484429 | 0.0868505 | intron-variant | Nedd4l | GRCm38.p3 | 18:65029305 | CAATGTTTCATCCAA[A/C]ATTCTGTTTTCTTTT | 83814 |
rs29767970 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Nedd4l | GRCm38.p3 | 18:65119753 | CAACATGCCTACTAA[C/T]TACTACATTAAATTA | 83814 |
rs29768221 | snp | C/T | 0.401235 | 0.199068 | intron-variant | Nedd4l | GRCm38.p3 | 18:65158249 | TGGATTCTTCATTGG[C/T]TTGAGTCACCTTGCC | 83814 |
rs29768655 | snp | C/T | 0.493827 | 0.0552116 | intron-variant | Nedd4l | Mm_Celera | 18:65202363 | CCCACCTTGTTGCCA[C/T]GGCCTCATTATTTAA | 83814 |
rs29769122 | snp | C/T | 0.304688 | 0.243945 | intron-variant | Nedd4l | GRCm38.p3 | 18:65194387 | AGAAACCATCTACAG[C/T]AGAGCTTGTGTGCTG | 83814 |
rs29769845 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Nedd4l | Mm_Celera | 18:65098878 | CTTTTATAACTTCAG[G/T]TTACAGGACTTTAGA | 83814 |
rs29769991 | snp | A/T | 0.375 | 0.216506 | intron-variant | Nedd4l | Mm_Celera | 18:64891612 | GAATGGGCCTGTTGG[A/T]CCCAGAGCCCTACTT | 83814 |
rs29770038 | snp | A/G | 0.484429 | 0.0868505 | intron-variant | Nedd4l | GRCm38.p3 | 18:65037610 | AAGTTTCAGTGTTAC[A/G]CATCCTACTGGACCG | 83814 |
rs29770931 | snp | A/G | 0.32 | 0.24 | intron-variant | Nedd4l | GRCm38.p3 | 18:65095943 | AGGGACAGAGTGAGC[A/G]GTCGAGGGTATTGGG | 83814 |
rs29771053 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Nedd4l | Mm_Celera | 18:65073138 | TGGGGATGTATGGGT[G/T]GGTGGGTGGGTTTAT | 83814 |
rs29771846 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Nedd4l | GRCm38.p3 | 18:64941390 | GCCTGCCTCTGCCTC[C/T]CAAGTGCTGGGATTA | 83814 |
rs29772026 | snp | C/T | 0.5 | 0 | intron-variant | Nedd4l | Mm_Celera | 18:65202347 | GCAGAGCCACCCTTG[C/T]CCCACCTTGTTGCCA | 83814 |
rs29772072 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Nedd4l | Mm_Celera | 18:65197162 | GCCCATGATGCCAGC[C/T]AGAGCTCACTGTGTT | 83814 |
rs29772115 | snp | A/G | 0.46875 | 0.121031 | intron-variant | Nedd4l | GRCm38.p3 | 18:65070548 | GCTATGCAATCAAGG[A/G]TGCTCTTCCCTTCCT | 83814 |
rs29772607 | snp | A/G | 0.492188 | 0.0620098 | intron-variant | Nedd4l | Mm_Celera | 18:65038827 | CCAAGATCCTCTAAG[A/G]AAGAGCAGTTTCTAA | 83814 |
rs29773187 | snp | A/G | 0.207612 | 0.24638 | utr-variant-3-prime, nc-transcript-variant | Nedd4l | Mm_Celera | 18:65214607 | GTGAAGCCCTAGACG[A/G]TGGAATCCTACCAAG | 83814 |
rs29773262 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Nedd4l | GRCm38.p3 | 18:64971039 | GGCAAAATGTCAAAG[C/T]GTGGTCACTTTATCC | 83814 |
rs29773381 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Nedd4l | Mm_Celera | 18:65072707 | AGTTTTCCAAATGCA[A/G]ATCAGTTGCCTCTGC | 83814 |
rs29773901 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Nedd4l | GRCm38.p3 | 18:65206246 | AGTGCCAGTAGTGGT[A/G]CCTGCTACTGTGCTT | 83814 |
rs29773909 | snp | A/G | 0.5 | 0 | intron-variant | Nedd4l | GRCm38.p3 | 18:65110420 | CACTGTGGAGTAGGC[A/G]TTAATACCCTCATTG | 83814 |
rs29775260 | snp | C/G | 0.5 | 0 | intron-variant | Nedd4l | GRCm38.p3 | 18:65196468 | GTTAGACAGGCTGGC[C/G]CTCACAGGGCCCCAT | 83814 |
rs29776776 | snp | C/T | 0.375 | 0.216506 | intron-variant | Nedd4l | Mm_Celera | 18:65031106 | AATTAAAGTGAGCTC[C/T]CCACTTGATCGTCAT | 83814 |
rs29776785 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | Nedd4l | GRCm38.p3 | 18:65036161 | TTTAACTAAGCCTAC[A/G]TCCAGACTGGAGGCG | 83814 |
rs29776786 | snp | A/T | 0.46875 | 0.121031 | intron-variant | Nedd4l | GRCm38.p3 | 18:65073486 | TAAACTTAGCATTGA[A/T]AATAACAAGTAGGAG | 83814 |
rs29777970 | snp | A/G | 0.5 | 0 | intron-variant | Nedd4l | GRCm38.p3 | 18:65128802 | GTTTGTTTATTATAT[A/G]TAAGTACACTGTAGC | 83814 |
rs29778725 | snp | C/T | 0.487535 | 0.077957 | intron-variant | Nedd4l | Mm_Celera | 18:64987204 | GCTTTCCAGTCTCCT[C/T]CTTCTTTTTTTAAAA | 83814 |
rs29778746 | snp | C/T | 0.375 | 0.216506 | intron-variant | Nedd4l | GRCm38.p3 | 18:64934554 | GCCTTTGTTGGCTCG[C/T]CCAAAGTACCATGAT | 83814 |
rs29778749 | snp | C/T | 0.5 | 0 | intron-variant | Nedd4l | GRCm38.p3 | 18:65210864 | ACTTTTTTTTTACTC[C/T]CACTTTAAATTGGTT | 83814 |
rs29778998 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Nedd4l | Mm_Celera | 18:65098041 | CACACACACGCGCGC[A/G]CGCGCACACACACAC | 83814 |
rs29779905 | snp | C/G | 0.32 | 0.24 | intron-variant | Nedd4l | GRCm38.p3 | 18:64986369 | TCTTCTTCTTTACCT[C/G]CATGACAAGTTTTGT | 83814 |
rs29779907 | snp | C/T | 0.5 | 0 | intron-variant | Nedd4l | GRCm38.p3 | 18:65148877 | GGGGTTGATCTGAGG[C/T]GATCAGGCTTGGTAG | 83814 |
rs29780732 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Nedd4l | Mm_Celera | 18:65167197 | GCTGCGCTCATGGAC[A/C]CCCCCCCCCCCACCA | 83814 |
rs29782013 | snp | C/T | 0.375 | 0.216506 | intron-variant | Nedd4l | GRCm38.p3 | 18:65106625 | AGCAGATTTCCCAGG[C/T]TTGAGTGTCTCCAGA | 83814 |
rs29782091 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Nedd4l | Mm_Celera | 18:65129590 | CAGATCACACCGTCT[A/G]TAACTAAAATCTAAA | 83814 |
rs29782786 | snp | A/G | 0.375 | 0.216506 | intron-variant | Nedd4l | GRCm38.p3 | 18:65055140 | CCTGGGTCCTCCCTG[A/G]GTGATAATTAAGTTG | 83814 |
rs29783055 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Nedd4l | Mm_Celera | 18:65197205 | TGCGGGAGGCGAGAG[A/G]CGACTATTGCACTCT | 83814 |
rs29787276 | snp | A/C | 0.415225 | 0.187619 | intron-variant | Nedd4l | GRCm38.p3 | 18:65135388 | CCAAAACATGACCAG[A/C]GGAGAAAAGAGACCT | 83814 |
rs29808036 | snp | G/T | 0.375 | 0.216506 | intron-variant | Nedd4l | Mm_Celera | 18:64891180 | GACTGGTATCTTTTT[G/T]GGGGGGAAAGGGGGT | 83814 |
rs29811871 | snp | A/G | 0.5 | 0 | downstream-variant-500B, nc-transcript-variant | Nedd4l, LOC105246470 | GRCm38.p3 | 18:65218245 | ATTCAATCTCTTGGG[A/G]CTGGAGAGATGACCC | 83814 |
rs29812465 | snp | A/G | 0.375 | 0.216506 | intron-variant | Nedd4l | GRCm38.p3 | 18:64901853 | CGAGTTCTAAATGTT[A/G]ATGTAGTTATATATT | 83814 |
rs29813412 | snp | A/G | 0.465374 | 0.126941 | intron-variant | Nedd4l | Mm_Celera | 18:65110665 | TGAGACAGGATGATG[A/G]GAAGGGTATATAGAA | 83814 |
rs29815893 | snp | A/G | 0.493827 | 0.0552116 | intron-variant | Nedd4l | Mm_Celera | 18:65072017 | TCTCACCTCATTCAC[A/G]AGTAGCCCGAAGGTG | 83814 |
rs29815960 | snp | A/G/T | 0.375 | 0.216506 | intron-variant | Nedd4l | GRCm38.p3 | 18:64991327 | GACAGCTCAGGTTTC[A/G/T]GCTCTCTACTGCCAT | 83814 |
rs29817072 | snp | A/G | 0.207612 | 0.24638 | intron-variant | Nedd4l | GRCm38.p3 | 18:65120405 | CAACCATGTACCCTC[A/G]GGTCCAGGAATCAGA | 83814 |
rs29817118 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Nedd4l | Mm_Celera | 18:65112785 | GAGCGGCTCCCTCTC[C/T]ATCACCTCGCACTAG | 83814 |
rs29817213 | snp | C/T | 0.265928 | 0.249492 | intron-variant | Nedd4l | Mm_Celera | 18:65099587 | TGGGTGCGCTTGAAA[C/T]GAGATTGTTAGCAAA | 83814 |
rs29817879 | snp | A/G | 0.375 | 0.216506 | intron-variant, upstream-variant-2KB | Nedd4l, A330084C13Rik | GRCm38.p3 | 18:64889919 | TGCCACTTTCGCCTT[A/G]GAGAATCACTGTTGA | 83814 |
rs29817932 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Nedd4l | GRCm38.p3 | 18:64896310 | GTTTCTGCTTCCTGT[C/G]TCCCAGGCAGAGGGC | 83814 |
rs29819430 | snp | A/G | 0.498615 | 0.0262793 | intron-variant | Nedd4l | Mm_Celera | 18:65184078 | CACCCAAGACAAGCC[A/G]ACAGATATTTGACAG | 83814 |
rs29819600 | snp | A/G | 0.487535 | 0.077957 | intron-variant | Nedd4l | GRCm38.p3 | 18:65135452 | TACAAAGCTTGTTTC[A/G]TAGAGCCCTGAGGAA | 83814 |
rs29819778 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Nedd4l | GRCm38.p3 | 18:64925937 | GGCGGTTGAGGTCAT[A/G]TATATCTCTCAGGTC | 83814 |
rs29819779 | snp | A/G | 0.375 | 0.216506 | intron-variant | Nedd4l | GRCm38.p3 | 18:64935331 | GCATTTGCAGAATCA[A/G]CAGAGCTCCTCTTCC | 83814 |
rs29821512 | snp | A/G | 0.375 | 0.216506 | intron-variant | Nedd4l | GRCm38.p3 | 18:64968062 | TGAAACTCAAGCTAC[A/G]AAAAAAAAAAAGTTT | 83814 |
rs29823263 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Nedd4l | GRCm38.p3 | 18:65202237 | AAAAGGAAGCAGCAG[C/T]AGCTGCTGGTGTCCA | 83814 |
rs29823519 | snp | C/T | 0.375 | 0.216506 | intron-variant | Nedd4l | Mm_Celera | 18:65183192 | AGATGTGCCCAGAAG[C/T]CGAGCCATCAGCCAG | 83814 |
rs29824066 | snp | A/G | 0.5 | 0 | intron-variant | Nedd4l | Mm_Celera | 18:65182868 | GTTCTCCCCCAGACA[A/G]CTTTAATCACCTGGT | 83814 |
rs29824853 | snp | A/G | 0.33241 | 0.236027 | intron-variant | Nedd4l | GRCm38.p3 | 18:65118786 | GCTAGAATCTCAGAG[A/G]AGTTTCATAGTATTT | 83814 |
rs29825786 | snp | A/G | 0.444444 | 0.157135 | intron-variant, upstream-variant-2KB | Nedd4l, A330084C13Rik | GRCm38.p3 | 18:64888698 | CTGCCATTTCTCTCC[A/G]GTCCAGAGAATTCAA | 83814 |
rs29826199 | snp | C/G | 0.375 | 0.216506 | intron-variant | Nedd4l | Mm_Celera | 18:64916532 | TTTTTTAGGAACTTG[C/G]ATCCTAAGTAGAAAT | 83814 |
rs29828916 | snp | G/T | 0.336735 | 0.234472 | intron-variant | Nedd4l | Mm_Celera | 18:65087708 | CCCAGCAAAGCCTCT[G/T]GGCTTTTACAGAAAA | 83814 |
rs29829446 | snp | A/C | 0.375 | 0.216506 | intron-variant | Nedd4l | Mm_Celera | 18:64891589 | GCGTGAATAATATTC[A/C]GGTGGGTGAATGGGC | 83814 |
rs29830095 | snp | C/T | 0 | 0 | intron-variant | Nedd4l | GRCm38.p3 | 18:65155796 | CCTGGCTGCCCAGCT[C/T]ACCTGAATGTCGTTC | 83814 |
rs29831994 | snp | A/G | 0.5 | 0 | intron-variant | Nedd4l | GRCm38.p3 | 18:64950364 | CCTCTACATGCTCAT[A/G]CACACATATGTATGT | 83814 |
rs29832025 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Nedd4l | GRCm38.p3 | 18:65132631 | GATTATACAGTGCCC[A/C]CCTCTACTGAAAGGA | 83814 |
rs29832616 | snp | A/C | 0.5 | 0 | intron-variant | Nedd4l | GRCm38.p3 | 18:65211068 | AGGACAAAATTCCCC[A/C]TAGCGACATCAATTT | 83814 |
rs29833074 | snp | A/G | 0.33241 | 0.236027 | intron-variant | Nedd4l | Mm_Celera | 18:65106513 | GCCTCTGGAGTGCAG[A/G]GCTGGATTTGACGGA | 83814 |
rs29834054 | snp | A/T | 0.456747 | 0.140554 | intron-variant | Nedd4l | GRCm38.p3 | 18:65010202 | TGTCTTCCTTCCTAA[A/T]TATTTTGGAGACGTA | 83814 |
rs29859708 | snp | A/G | 0.375 | 0.216506 | intron-variant | Nedd4l | Mm_Celera | 18:64987245 | TGTGTGTGCCTGCAT[A/G]CGCCATGGTGCATAT | 83814 |
rs29860657 | snp | G/T | 0.32 | 0.24 | intron-variant | Nedd4l | GRCm38.p3 | 18:65086176 | CCCCCAGTGAGGAAT[G/T]CCTTTCCTCAGGTTG | 83814 |
rs29860898 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Nedd4l | GRCm38.p3 | 18:65086400 | CCTTTGAGGAAGGAG[C/T]CATGTATCAGATATT | 83814 |
rs29861699 | snp | C/T | 0.42 | 0.183303 | intron-variant | Nedd4l | Mm_Celera | 18:65096171 | TTTTCTGTAAACCAC[C/T]GGCCACCAGATTTTT | 83814 |
rs29863048 | snp | C/T | 0.32 | 0.24 | intron-variant | Nedd4l | Mm_Celera | 18:64891103 | GCCATCTGTAGTCCG[C/T]GTTGGCATGGTTTAC | 83814 |
rs29864017 | snp | C/G | 0.375 | 0.216506 | intron-variant | Nedd4l | GRCm38.p3 | 18:64932397 | GGAAGATGGTTGCTT[C/G]GGTGGGCAGGCCTGC | 83814 |
rs29864036 | snp | A/G | 0.487535 | 0.077957 | intron-variant | Nedd4l | GRCm38.p3 | 18:65088426 | GGTAGGAGGCAGCTA[A/G]GGCCCTCAGCAGGCT | 83814 |
rs29865095 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Nedd4l | Mm_Celera | 18:65129561 | CCAGATTCCATTCCC[A/T]GCGTCCCACAAGGCA | 83814 |
rs29867015 | snp | A/C | 0.5 | 0 | intron-variant | Nedd4l | Mm_Celera | 18:64940969 | CACACACACACACAC[A/C]CCACACAGGAGAATT | 83814 |
rs29867328 | snp | A/G | 0.5 | 0 | intron-variant | Nedd4l | GRCm38.p3 | 18:65101160 | CTGATTCCATCTGTT[A/G]GCTTATCCTGTACCT | 83814 |
rs29867946 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Nedd4l | Mm_Celera | 18:65077912 | ATTTTGAAGATCTGT[A/G]GAGGTTTCATTTGGA | 83814 |
rs29868348 | snp | A/C/T | 0.444444 | 0.157135 | intron-variant | Nedd4l | GRCm38.p3 | 18:65112778 | TCCTTGGGAGCGGCT[A/C/T]CCTCTCTATCACCTC | 83814 |
rs29869044 | snp | A/G | 0.5 | 0 | intron-variant, upstream-variant-2KB | Nedd4l | GRCm38.p3 | 18:65023371 | TTGTAGCCATTTAGG[A/G]ACCAGTCGGGAGGAC | 83814 |
rs29870202 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Nedd4l | GRCm38.p3 | 18:65069399 | GCTGGCAGGCAAGGT[A/G]GTGACTTGGCAGCCT | 83814 |
rs29872992 | snp | C/T | 0.375 | 0.216506 | intron-variant | Nedd4l | Mm_Celera | 18:65168703 | AAAAGACAGAGCAAA[C/T]TGACTGTGGTAAATA | 83814 |
rs29873749 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Nedd4l | GRCm38.p3 | 18:65029702 | TCTGATTCCTGTCTC[C/T]TGATTCTCCCTTCAC | 83814 |
rs29873990 | snp | C/G | 0.375 | 0.216506 | intron-variant | Nedd4l | GRCm38.p3 | 18:65027038 | TTAGGAGTTCAAGGT[C/G]ATTCTTGGCTACAAA | 83814 |
rs29874234 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Nedd4l | GRCm38.p3 | 18:64937511 | GAAGAGAAGGTGTTA[C/T]GCATGCCCTCAAAAA | 83814 |
rs29874250 | snp | A/T | 0.387812 | 0.208586 | intron-variant | Nedd4l | GRCm38.p3 | 18:65085116 | GCTATAAAAAATAAG[A/T]CAGCACCTAGATGTG | 83814 |
rs29874616 | snp | C/G | 0.375 | 0.216506 | intron-variant | Nedd4l | Mm_Celera | 18:64979757 | GGATTCTTTCCTCTG[C/G]CCACTTGTCATTTTC | 83814 |
rs29874621 | snp | C/T | 0.32 | 0.24 | intron-variant, upstream-variant-2KB | Nedd4l, A330084C13Rik | Mm_Celera | 18:64890218 | GCCTCCATATTTTTA[C/T]GGTATCTGTTTGGTA | 83814 |
rs29875758 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Nedd4l | GRCm38.p3 | 18:64983421 | TGGGTGTAATTTGGA[G/T]AGGAGCTGGCACCTG | 83814 |
rs29879205 | snp | C/T | 0.429688 | 0.173817 | intron-variant | Nedd4l | GRCm38.p3 | 18:65005174 | GTGAGCCCTTAGTAC[C/T]GACTTGAATGTGATT | 83814 |
rs29879846 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Nedd4l | GRCm38.p3 | 18:65057479 | GGGTGGCTCATTAGT[A/G]CTTAGAGGGCAAAGT | 83814 |
rs29882605 | snp | A/G | 0.5 | 0 | intron-variant | Nedd4l | GRCm38.p3 | 18:65210952 | TCCGTTGGATCACTG[A/G]GACCCACAGGGTGGA | 83814 |
rs29883120 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Nedd4l | GRCm38.p3 | 18:65080752 | AACTCTCAAAGACGA[A/G]CTTGAAGAAGAGCTG | 83814 |
rs29884982 | snp | C/T | 0.493827 | 0.0552116 | intron-variant, upstream-variant-2KB | Nedd4l | Mm_Celera | 18:65074249 | TTTCTCAAGTCTCTA[C/T]CTTTGGGTGACCACC | 83814 |
rs29885298 | snp | C/T | 0.465374 | 0.126941 | utr-variant-3-prime, nc-transcript-variant | Nedd4l, LOC105246470 | GRCm38.p3 | 18:65217729 | AGCTTGTTTTTCTGA[C/T]GGCAAATGGGAACTG | 83814 |
rs29886809 | snp | C/G | 0.465374 | 0.126941 | utr-variant-3-prime, nc-transcript-variant | Nedd4l | GRCm38.p3 | 18:65214258 | AGTGACCTAGAAAGC[C/G]CAGTAGGAACCACAG | 83814 |
rs29907674 | snp | C/T | 0.49827 | 0.0293608 | intron-variant | Nedd4l | Mm_Celera | 18:65072081 | TACAGCAGAGCCCTG[C/T]ACACTAGTAACTGCT | 83814 |
rs29908434 | snp | A/G | 0.48 | 0.0979796 | utr-variant-3-prime, nc-transcript-variant | Nedd4l | Mm_Celera | 18:65213578 | CAAATTTAGATACTA[A/G]GTCCAGGCTGGAAGA | 83814 |
rs29909537 | snp | A/G | 0.5 | 0 | intron-variant | Nedd4l | GRCm38.p3 | 18:65068274 | CTTTAAAAGTCCCTC[A/G]TGGTCATGTGTTGAA | 83814 |
rs29910318 | snp | A/G | 0.456747 | 0.140554 | intron-variant | Nedd4l | GRCm38.p3 | 18:65005128 | GTACATGATTGGGTC[A/G]CTGTCATTCGTGGGG | 83814 |
rs29911662 | snp | A/G | 0.492188 | 0.0620098 | intron-variant | Nedd4l | GRCm38.p3 | 18:65041506 | ATCTTCTGACCCCTA[A/G]CCGCATACAGACAGT | 83814 |
rs29911713 | snp | G/T | 0.375 | 0.216506 | intron-variant | Nedd4l | Mm_Celera | 18:64922934 | CTTTGGAGCGTCTTA[G/T]ATTTTGAGTTGAATC | 83814 |
rs29911866 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Nedd4l | Mm_Celera | 18:65197185 | ACTGTGTTTCTGCTC[A/G]GTGCTGCGGGAGGCG | 83814 |
rs29911966 | snp | A/G | 0.375 | 0.216506 | intron-variant | Nedd4l | Mm_Celera | 18:64970078 | ATTTACATTTCAAAT[A/G]CTATCCCAAAAGTCC | 83814 |
rs29912022 | snp | A/C | 0.48 | 0.0979796 | intron-variant | Nedd4l | Mm_Celera | 18:65073563 | ACTCCAGAAGTGGTT[A/C]CCATTGTTGGGATGG | 83814 |
rs29912626 | snp | C/T | 0.456747 | 0.140554 | intron-variant | Nedd4l | GRCm38.p3 | 18:65031435 | CCTCCACTTTCCAGG[C/T]GTGATTTGTTTCATA | 83814 |
rs29912820 | snp | A/G | 0.46875 | 0.121031 | intron-variant | Nedd4l | GRCm38.p3 | 18:65037388 | ACACTTAAAAACATA[A/G]GGCTGATTCATTAGC | 83814 |
rs29914254 | snp | A/G | 0.475309 | 0.108333 | intron-variant | Nedd4l | Mm_Celera | 18:65119388 | TCTTGCACATGGCCT[A/G]TGGCTAGTGTGCCTC | 83814 |
rs29914608 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Nedd4l | GRCm38.p3 | 18:65086358 | GAACTATGTAGATCA[C/T]TGGTCCTCAATGTGT | 83814 |
rs29916574 | snp | A/G | 0.375 | 0.216506 | intron-variant | Nedd4l | Mm_Celera | 18:65096565 | CTTCTCCATTTGACA[A/G]TACTGGACAAGAAGC | 83814 |
rs29917212 | snp | A/G | 0.5 | 0 | intron-variant, upstream-variant-2KB | Nedd4l | Mm_Celera | 18:65073893 | GGGGGGGGGATGCAT[A/G]AAGAGGTCAGAAGAT | 83814 |
rs29920434 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Nedd4l | GRCm38.p3 | 18:65125468 | TAAGCAGAAAGGCAG[A/G]CAGGCCACCTGGCAT | 83814 |
rs29920513 | snp | C/T | 0.487535 | 0.077957 | intron-variant | Nedd4l | GRCm38.p3 | 18:65136233 | GTACTGAGGGAAGGA[C/T]GTAAGCGCAGAGCTC | 83814 |
rs29920859 | snp | A/C | 0.487535 | 0.077957 | intron-variant | Nedd4l | GRCm38.p3 | 18:64981080 | GAGGTTTCTCGGAAC[A/C]AAAGTTACCTAGTTA | 83814 |
rs29921706 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Nedd4l | GRCm38.p3 | 18:65100319 | CTTAGGCAGATGTGA[A/G]CTGCCCACTGTGGGT | 83814 |
rs29921710 | snp | A/T | 0.5 | 0 | intron-variant | Nedd4l | GRCm38.p3 | 18:65205844 | CTTCTCTCCATTTTT[A/T]ATTTGTTTTAATAGC | 83814 |
rs29921993 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Nedd4l | Mm_Celera | 18:64987290 | GTAAATGAATGGATA[A/G]ATTGGTTCTCTCTGT | 83814 |
rs29923318 | snp | C/T | 0.32 | 0.24 | intron-variant | Nedd4l | GRCm38.p3 | 18:65069318 | AAAGGAGAATGATAA[C/T]TTCCTTCAATATGGA | 83814 |
rs29923862 | snp | C/T | 0.5 | 0 | intron-variant | Nedd4l | Mm_Celera | 18:64977937 | TTTTGTGAAGTATCC[C/T]AGTGTCTCATTATTT | 83814 |
rs29925058 | snp | A/G | 0.375 | 0.216506 | intron-variant | Nedd4l | GRCm38.p3 | 18:65041243 | CACAGAATGTGAGGG[A/G]AGGATGCTGAGAAAG | 83814 |
rs29925404 | snp | A/G | 0.46875 | 0.121031 | intron-variant | Nedd4l | GRCm38.p3 | 18:65041636 | AACCCTTGTGTAGTA[A/G]AAGATACATGATTTA | 83814 |
rs29925755 | snp | A/G | 0.5 | 0 | intron-variant | Nedd4l | GRCm38.p3 | 18:65041451 | GGTGGCAGGAAGGAC[A/G]CAGGGATGATTCTGT | 83814 |
rs29925865 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Nedd4l | Mm_Celera | 18:65062614 | CCTCTGCCATTTGGA[A/G]TAAGCCTTCTTTAGG | 83814 |
rs29927435 | snp | C/T | 0.486111 | 0.0821678 | intron-variant | Nedd4l | Mm_Celera | 18:65073543 | TTCCTGTAGTCTTTG[C/T]GAATACTCCAGAAGT | 83814 |
rs29928779 | snp | A/C | 0.197531 | 0.244432 | intron-variant | Nedd4l | GRCm38.p3 | 18:65078150 | TATGGTCTGCTCATC[A/C]ACTGTAGGAAGATGA | 83814 |
rs29928929 | snp | C/G | 0.375 | 0.216506 | intron-variant | Nedd4l | GRCm38.p3 | 18:64921484 | GCTGATGGGTGGTGC[C/G]GGAGACAGGAAGATA | 83814 |
rs29930314 | snp | C/T | 0.465374 | 0.126941 | intron-variant | Nedd4l | Mm_Celera | 18:65194311 | AAACCAAGAGACGAA[C/T]GAACCTTTAGGGGAA | 83814 |
rs29932065 | snp | A/G | 0.484429 | 0.0868505 | intron-variant | Nedd4l | GRCm38.p3 | 18:65036241 | TGACTTAATTGCATG[A/G]CTCTTAAAACTTTCA | 83814 |
rs29933097 | snp | C/G | 0.48 | 0.0979796 | intron-variant | Nedd4l | GRCm38.p3 | 18:65088691 | GTGGAGGCTGGGGTT[C/G]TTTTTGTTTGTTCTT | 83814 |
rs29934096 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Nedd4l | Mm_Celera | 18:65197187 | TGTGTTTCTGCTCGG[C/T]GCTGCGGGAGGCGAG | 83814 |
rs29956683 | snp | A/G | 0.498615 | 0.0262793 | intron-variant | Nedd4l | Mm_Celera | 18:65107151 | TCTGTACACAAGCTC[A/G]TGAAAAAATGGTGGT | 83814 |
rs29958004 | snp | A/C | 0.375 | 0.216506 | intron-variant | Nedd4l | Mm_Celera | 18:64969428 | TTTTTGCTATGGTAA[A/C]ATGATGCTGTGTCAT | 83814 |
rs29958907 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Nedd4l | GRCm38.p3 | 18:65202160 | GTTTCTAGGAAGGAG[A/G]GAAACTGGGAAAGGG | 83814 |
rs29960932 | snp | A/G | 0.475309 | 0.108333 | intron-variant | Nedd4l | GRCm38.p3 | 18:64985654 | TGCCCTTGGTTCGGT[A/G]ACTGCCTCCTCTACT | 83814 |
rs29961093 | snp | C/T | 0.492188 | 0.0620098 | intron-variant | Nedd4l | GRCm38.p3 | 18:64988499 | TGGAGTTGAACTTGA[C/T]TTTGTGTCCTGTGTT | 83814 |
rs29961325 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Nedd4l | GRCm38.p3 | 18:64939572 | GGATCTTATAGGGTC[A/G]CCTTTGCAGAGTATC | 83814 |
rs29964095 | snp | A/G | 0.375 | 0.216506 | intron-variant | Nedd4l | GRCm38.p3 | 18:65158779 | AGCAGAATTAATATT[A/G]ACAAGTAGTTATTAC | 83814 |
rs29964359 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Nedd4l | GRCm38.p3 | 18:64939967 | AGTGGGTAGTCTCAG[C/T]CAGCAGCGAGGAAGC | 83814 |
rs29965785 | snp | A/G | 0.5 | 0 | intron-variant | Nedd4l | GRCm38.p3 | 18:65062270 | CAGGGCTGGGTGCCT[A/G]CCCAAAGACACTTAG | 83814 |
rs29966578 | snp | C/T | 0.455 | 0.143091 | intron-variant | Nedd4l | Mm_Celera | 18:65064285 | GGTGTGCATCCGCAT[C/T]TCCTGTGAGCAGCCT | 83814 |
rs29966931 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Nedd4l | Mm_Celera | 18:65188572 | GGGAGGGGGAAGTGT[A/G]GGGAGAGACTAAAGA | 83814 |
rs29967494 | snp | C/T | 0.5 | 0 | intron-variant | Nedd4l | GRCm38.p3 | 18:65209568 | TCCATGCAGTGTAAA[C/T]GAGAATTTGGTTGCC | 83814 |
rs29967531 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Nedd4l | GRCm38.p3 | 18:64997122 | TGTAGCCGAAGGTGG[C/T]CTCGAGAACTTCCTA | 83814 |
rs29968086 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Nedd4l | Mm_Celera | 18:65164123 | GTCATTCTCATGTAC[A/G]TACAGAATTAAGACC | 83814 |
rs29968461 | snp | C/G | 0.493827 | 0.0552116 | intron-variant | Nedd4l | Mm_Celera | 18:65182810 | AATCTAGTGTGTGCA[C/G]TACAAAATCCCTGTG | 83814 |
rs29969014 | snp | C/T | 0.444444 | 0.157135 | intron-variant, upstream-variant-2KB | Nedd4l, LOC105246471 | GRCm38.p3 | 18:65052004 | GTTTAGTAGTGTATC[C/T]GTAAGCCTGGAATAC | 83814 |
rs29969377 | snp | A/G | 0.415225 | 0.187619 | intron-variant | Nedd4l | GRCm38.p3 | 18:64924071 | GTGCTGGAGTCGGAT[A/G]TGTGTGTAATTTCCT | 83814 |
rs29969833 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Nedd4l | GRCm38.p3 | 18:65064788 | ACTGCTGGTTCCTCG[A/G]TTCCTCAGCAGCCCT | 83814 |
rs29970124 | snp | A/G | 0.375 | 0.216506 | upstream-variant-2KB, nc-transcript-variant | Nedd4l, A330084C13Rik | GRCm38.p3 | 18:64886284 | CCATACTTAGGAGCA[A/G]TCCTCTCTCTCTCCT | 83814 |
rs29973037 | snp | C/G | 0.415225 | 0.187619 | intron-variant | Nedd4l | GRCm38.p3 | 18:64970815 | GATATTTCTTATTCA[C/G]TCCACTACATTGCCC | 83814 |
rs29974248 | snp | C/T | 0.401235 | 0.199068 | intron-variant | Nedd4l | Mm_Celera | 18:65178634 | CTGTTCTTAAAGGGT[C/T]ACATTTAGAGACTAT | 83814 |
rs29974401 | snp | A/G | 0.33241 | 0.236027 | intron-variant | Nedd4l | GRCm38.p3 | 18:65072030 | ACGAGTAGCCCGAAG[A/G]TGAGTGTGGTTAAGC | 83814 |
rs29976005 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Nedd4l | GRCm38.p3 | 18:65118451 | ATGTCAGAGGGAAAT[A/G]CAGTATTAGGGTATA | 83814 |
rs29977382 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Nedd4l | GRCm38.p3 | 18:64935248 | TCCCAGTCGACCCAG[C/T]TCTATCGCTTACCTC | 83814 |
rs29977503 | snp | A/G | 0.197531 | 0.244432 | intron-variant | Nedd4l | GRCm38.p3 | 18:65194967 | GGTTGCCCATGCACT[A/G]TAAAATGAAGCAATG | 83814 |
rs29977822 | snp | A/C | 0.498615 | 0.0262793 | intron-variant | Nedd4l | GRCm38.p3 | 18:64932289 | GTCGTTTTTTTAGCC[A/C]GTTCTCTCCAAAGAC | 83814 |
rs29980009 | snp | A/G | 0.5 | 0 | intron-variant | Nedd4l | GRCm38.p3 | 18:65109321 | TTTTCTACTTCAGGG[A/G]TAAAGGGGGTGTTCC | 83814 |
rs29981708 | snp | A/G | 0.387812 | 0.208586 | utr-variant-3-prime, nc-transcript-variant | Nedd4l | GRCm38.p3 | 18:65214144 | TACTGTATACACTTA[A/G]CCAAGTTGTGTGACC | 83814 |
rs29982301 | snp | A/G | 0.456747 | 0.140554 | intron-variant | Nedd4l | GRCm38.p3 | 18:65041318 | AATTCGGTGGAACCA[A/G]ACAGAGAGTGCGTGG | 83814 |
rs29982386 | snp | C/G | 0.5 | 0 | intron-variant | Nedd4l | GRCm38.p3 | 18:64907332 | ATGTTGTGCCCTCGA[C/G]TGGGATTAAGATATT | 83814 |
rs29996333 | snp | G/T | 0.455 | 0.143091 | intron-variant | Nedd4l | Mm_Celera | 18:65175598 | TTCATTTGGTAAACC[G/T]ATAACTACTTCAGAG | 83814 |
rs29999607 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Nedd4l | Mm_Celera | 18:65061927 | ATTCAGTGTCTCTCC[A/G]GGGCCCCACAGGTTC | 83814 |
rs30002553 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Nedd4l | Mm_Celera | 18:65072728 | TTGCCTCTGCATCAG[A/G]GAATTTTTCTAGAAA | 83814 |
rs30003452 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Nedd4l | GRCm38.p3 | 18:64934463 | TTCCTTTTAAAAAAT[C/T]GGAAATAAATAAAAA | 83814 |
rs30005103 | snp | C/T | 0.415225 | 0.187619 | intron-variant | Nedd4l | GRCm38.p3 | 18:65106652 | CAGAAGGCAGGAAGC[C/T]GCCATGCCGTGCCAT | 83814 |
rs30006975 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Nedd4l | Mm_Celera | 18:65038040 | GGATTACCAGCACCA[C/T]GCCCGGCAAGCACTG | 83814 |
rs30007945 | snp | C/T | 0.429688 | 0.173817 | intron-variant | Nedd4l | GRCm38.p3 | 18:65136044 | CACAGTGTGAGAGTA[C/T]GCAGCAACACACTGT | 83814 |
rs30008670 | snp | A/C/G | 0.375 | 0.216506 | intron-variant | Nedd4l | Mm_Celera | 18:65082654 | TCTCTCTCTCTCTCT[A/C/G]TCTCTCTCTCTCTCT | 83814 |
rs30009673 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Nedd4l | GRCm38.p3 | 18:65158060 | CACCCTGCACAGCAA[C/T]GGGTGGCAGTTCCAG | 83814 |
rs30009770 | snp | C/T | 0.35503 | 0.226867 | intron-variant | Nedd4l | GRCm38.p3 | 18:64934552 | CAGCCTTTGTTGGCT[C/T]GCCCAAAGTACCATG | 83814 |
rs30010771 | snp | C/T | 0.5 | 0 | intron-variant | Nedd4l | Mm_Celera | 18:65196921 | AAGTGTGTATCTGTG[C/T]GTGTATATGTGTGTG | 83814 |
rs30010903 | snp | G/T | 0.487535 | 0.077957 | intron-variant | Nedd4l | GRCm38.p3 | 18:65096902 | AGCAGCTGGGTAAGC[G/T]GATGCAGCTGACATC | 83814 |
rs30011622 | snp | A/G | 0.401235 | 0.199068 | intron-variant | Nedd4l | GRCm38.p3 | 18:65088283 | GTGCGTTATGTGCAT[A/G]TGACTGTATACTCAC | 83814 |
rs30011681 | snp | C/G | 0.32 | 0.24 | intron-variant | Nedd4l | GRCm38.p3 | 18:65086182 | GTGAGGAATGCCTTT[C/G]CTCAGGTTGACGTGA | 83814 |
rs30012993 | snp | C/T | 0.432133 | 0.171253 | intron-variant | Nedd4l | Mm_Celera | 18:65091711 | GTATTCTAATTCCTG[C/T]TGTCAGACACCGATG | 83814 |
rs30013034 | snp | A/C | 0.396694 | 0.202437 | intron-variant | Nedd4l | GRCm38.p3 | 18:65029759 | GCAAATGTATTCTTT[A/C]TGTTGTCTTCTAACC | 83814 |
rs30013929 | snp | A/G | 0.484429 | 0.0868505 | intron-variant | Nedd4l | Mm_Celera | 18:65173211 | ATGCTTTGGGGTCTC[A/G]GTCAGCTAACATTCT | 83814 |
rs30014229 | snp | C/T | 0.49827 | 0.0293608 | intron-variant, upstream-variant-2KB | Nedd4l | Mm_Celera | 18:65074263 | ATCTTTGGGTGACCA[C/T]CGAATTTTCTAGGCT | 83814 |
rs30015635 | snp | C/T | 0.42 | 0.183303 | intron-variant | Nedd4l | GRCm38.p3 | 18:64986171 | CCCTTGCGGACTGTT[C/T]TTTTGCCTTCTACCT | 83814 |
rs30016199 | snp | C/T | 0.32 | 0.24 | intron-variant | Nedd4l | GRCm38.p3 | 18:64934804 | TAATTACTAAATACT[C/T]CAAATACAGTGTGTG | 83814 |
rs30016275 | snp | G/T | 0.492188 | 0.0620098 | intron-variant | Nedd4l | Mm_Celera | 18:64987494 | GCAAGCATGCAGCTC[G/T]GTCTGCAAAATTTTA | 83814 |
rs30016787 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Nedd4l | GRCm38.p3 | 18:64963857 | GATTGTCCTCTGAGG[G/T]ACAAATGTGTCCCTG | 83814 |
rs30018353 | snp | A/G | 0.415225 | 0.187619 | intron-variant | Nedd4l | Mm_Celera | 18:65202380 | GCCTCATTATTTAAT[A/G]TGAATAGTCTAGTCT | 83814 |
rs30019830 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Nedd4l | GRCm38.p3 | 18:65053969 | CTTACTCATGTGGCC[C/T]GCTGCAGGCAGAGAG | 83814 |
rs30019977 | snp | A/G | 0.290657 | 0.246672 | intron-variant | Nedd4l | Mm_Celera | 18:65069084 | GATTTAAATAAGTAT[A/G]CAACTCTGATGGTAG | 83814 |
rs30020814 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Nedd4l | GRCm38.p3 | 18:65193941 | AAAGATTTAGCATTG[C/T]TCCAGAGTAGACTTC | 83814 |
rs30020971 | snp | C/T | 0.265928 | 0.249492 | intron-variant | Nedd4l | GRCm38.p3 | 18:65097039 | TCCGCAAAATTAATT[C/T]AGGACACCTGGGTGA | 83814 |
rs30021679 | snp | G/T | 0.375 | 0.216506 | intron-variant | Nedd4l | Mm_Celera | 18:65161434 | CTTAGTCGGTGCGTG[G/T]ACCACAGTGAGGGTT | 83814 |
rs30022337 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Nedd4l | GRCm38.p3 | 18:65012394 | ACGCAGGCCATTCTC[A/T]TTCAAACCACCAGCA | 83814 |
rs30022871 | snp | C/T | 0.456747 | 0.140554 | intron-variant | Nedd4l | GRCm38.p3 | 18:65010011 | AGCTTAAATATAGTT[C/T]GTGAAAGCTTTTGAT | 83814 |
rs30023071 | snp | C/G | 0.487535 | 0.077957 | intron-variant | Nedd4l | Mm_Celera | 18:65106525 | CAGAGCTGGATTTGA[C/G]GGAAGAAAGGAAAGC | 83814 |
rs30023072 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Nedd4l | Mm_Celera | 18:65098047 | CACGCGCGCGCGCGC[A/G]CACACACACACACAC | 83814 |
rs30024509 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Nedd4l | Mm_Celera | 18:65064430 | AACATCTGATCTCAC[C/T]GATATCTTAATTTTC | 83814 |
rs30024879 | snp | C/T | 0 | 0 | intron-variant | Nedd4l | GRCm38.p3 | 18:65149165 | ATTTCAAACTAGTGA[C/T]GAGCTGCTGTCTTGT | 83814 |
rs30026053 | snp | C/T | 0.5 | 0 | intron-variant | Nedd4l | GRCm38.p3 | 18:64986756 | GAGTTCTTCGTGCGA[C/T]TCACTGTGGGCCCAG | 83814 |
rs30026146 | snp | A/C | 0.32 | 0.24 | intron-variant | Nedd4l | Mm_Celera | 18:65099706 | AAAGTCTGACACTTT[A/C]CATATCTTATATTTC | 83814 |
rs30027059 | snp | C/T | 0.415225 | 0.187619 | intron-variant | Nedd4l | GRCm38.p3 | 18:65110288 | TGAAGAGAGTATCAC[C/T]CTTAAATCTGATCCC | 83814 |
rs30027697 | snp | A/T | 0.475309 | 0.108333 | intron-variant | Nedd4l | Mm_Celera | 18:64928163 | GAGACCATTGTCAAT[A/T]ACTGTGTGGAATAAT | 83814 |
rs30028023 | snp | A/G | 0.487535 | 0.077957 | intron-variant | Nedd4l | GRCm38.p3 | 18:64985172 | CCCTACATGTGTGCC[A/G]CTCTAACCAGAGTCA | 83814 |
rs30028915 | snp | A/C | 0.33241 | 0.236027 | intron-variant | Nedd4l | GRCm38.p3 | 18:65202320 | TCGGCCACCTGACAG[A/C]AGACCCAGTTGGCAG | 83814 |
rs30028917 | snp | C/T | 0.375 | 0.216506 | intron-variant | Nedd4l | GRCm38.p3 | 18:64956405 | TTCTTGGTCATGATG[C/T]TTGTGCAGGAATAGA | 83814 |
rs30029307 | snp | A/G | 0.5 | 0 | intron-variant, upstream-variant-2KB | Nedd4l | GRCm38.p3 | 18:65023095 | AGTGCTAAAGGGTAA[A/G]GAAGGGCTAAAAGCA | 83814 |
rs30029684 | snp | A/G | 0.465374 | 0.126941 | downstream-variant-500B, nc-transcript-variant | Nedd4l, LOC105246470 | GRCm38.p3 | 18:65218121 | ACTTCACCTCTGCTT[A/G]CCAGTGTGCCCCGGA | 83814 |
rs30030345 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Nedd4l | Mm_Celera | 18:65036450 | AAAACAAAAAACAAG[C/T]AAGCAAGCAAACAAA | 83814 |
rs30032038 | snp | A/G | 0.415225 | 0.187619 | intron-variant | Nedd4l | Mm_Celera | 18:65164219 | CACTAGGTGGGAGAC[A/G]GCATCCTCACACGAT | 83814 |
rs30032447 | snp | G/T | 0.415225 | 0.187619 | downstream-variant-500B, nc-transcript-variant | Nedd4l, LOC105246470 | GRCm38.p3 | 18:65218036 | TGTCTTTTTTTTTAT[G/T]AAACCTGAGCATTGC | 83814 |
rs30047010 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Nedd4l | GRCm38.p3 | 18:65114050 | GGCACCATCTGAAGT[C/T]GTGGCCTTGTTGGAA | 83814 |
rs30052431 | snp | C/T | 0.375 | 0.216506 | intron-variant | Nedd4l | Mm_Celera | 18:65070237 | TGGCTTTGAGCCACT[C/T]AAGCGTTCTCCTCTT | 83814 |
rs30058576 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Nedd4l | Mm_Celera | 18:64987174 | GATTGGGGTGTTGTG[C/T]TGGACTCACAAGCAG | 83814 |
rs30060573 | snp | A/G | 0.359862 | 0.224567 | intron-variant | Nedd4l | Mm_Celera | 18:64953912 | GTACTTTATTTCCTA[A/G]TTTTCAAGGCATTTA | 83814 |
rs30061805 | snp | A/T | 0.375 | 0.216506 | intron-variant | Nedd4l | GRCm38.p3 | 18:65039099 | AGGCAGGAACTGAAG[A/T]AGAAGCCATAGAGAA | 83814 |
rs30062565 | snp | C/T | 0.401235 | 0.199068 | intron-variant | Nedd4l | GRCm38.p3 | 18:65081860 | CTAAAATAATGACTG[C/T]AGTCGAGCGACCTTG | 83814 |
rs30062988 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Nedd4l | GRCm38.p3 | 18:64974060 | TGCTGTGTGCAAGCA[C/T]GGGGACTTGGGCCAG | 83814 |
rs30064025 | snp | A/G | 0.207612 | 0.24638 | intron-variant | Nedd4l | GRCm38.p3 | 18:65109498 | TGAGAGCCGCCAGAA[A/G]CAGTAAGGGATTTCT | 83814 |
rs30064618 | snp | A/G | 0.46875 | 0.121031 | intron-variant | Nedd4l | Mm_Celera | 18:65110232 | AATAAGGACCATTTG[A/G]GACACAAAGAAGTCT | 83814 |
rs30065148 | snp | C/T | 0.429688 | 0.173817 | intron-variant | Nedd4l | GRCm38.p3 | 18:65069231 | CATTAGCCCGGTGTG[C/T]TTTGGTAATGGGGAA | 83814 |
rs30065965 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Nedd4l | GRCm38.p3 | 18:65084039 | GGACCCGAGGACAGG[C/T]CCCCAAGCACCCAGG | 83814 |
rs30066151 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Nedd4l | GRCm38.p3 | 18:64931055 | ATATCCAAAGAGCTA[A/T]AGTCTAACTAAGGAT | 83814 |
rs30066346 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Nedd4l | Mm_Celera | 18:64931120 | GGACTTGCAGGCACA[C/G]TTTACTGGCGATCCC | 83814 |
rs30067007 | snp | A/T | 0.345679 | 0.230967 | intron-variant | Nedd4l | Mm_Celera | 18:65097351 | AAAAGAGGAGGGCTG[A/T]TGTCAGATTTTTGAC | 83814 |
rs30067090 | snp | A/C | 0.456747 | 0.140554 | intron-variant | Nedd4l | GRCm38.p3 | 18:65044117 | AAACCCATCACTTTT[A/C]TGTCTTTAATTAGTT | 83814 |
rs30071253 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Nedd4l | GRCm38.p3 | 18:65060494 | TTTCTAAATGTAATA[A/C]AACTCTGAGAAGCCA | 83814 |
rs30072701 | snp | C/T | 0.487535 | 0.077957 | intron-variant | Nedd4l | GRCm38.p3 | 18:65135338 | TCTCTCCCCTGCAAA[C/T]TGATGGAGTCCACTG | 83814 |
rs30072909 | snp | C/G | 0.5 | 0 | intron-variant | Nedd4l | Mm_Celera | 18:65082642 | TCTCTCTCTCTCTCT[C/G]TCTCTCTCTCTCTCT | 83814 |
rs30073305 | snp | A/G | 0.5 | 0 | intron-variant | Nedd4l | GRCm38.p3 | 18:65097910 | ACAGATTCTACTGGT[A/G]CCCGGCCAGTGAGCC | 83814 |
rs30074303 | snp | A/G | 0.429688 | 0.173817 | intron-variant | Nedd4l | GRCm38.p3 | 18:65001039 | GGTCAGTCAGCGGAA[A/G]CTCTGAGGTAGCATT | 83814 |
rs30075877 | snp | A/G | 0.32 | 0.24 | intron-variant | Nedd4l | GRCm38.p3 | 18:65056954 | AGCCACTGAAGGGGA[A/G]TGGGGAAAGGCCTGC | 83814 |
rs30077506 | snp | C/G | 0.46875 | 0.121031 | intron-variant | Nedd4l | GRCm38.p3 | 18:65109441 | GGTCCTGATGCTGCA[C/G]AACCAACTTCATGAC | 83814 |
rs30077898 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Nedd4l | GRCm38.p3 | 18:65135020 | TATGCTCATGGCAAA[C/T]ATACTTCAGGTTGTG | 83814 |
rs30084184 | snp | A/T | 0.375 | 0.216506 | intron-variant | Nedd4l | GRCm38.p3 | 18:65055514 | ATGGGGTTAAGAGCC[A/T]TAAAGAGAAGCAGTC | 83814 |
rs30102540 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Nedd4l | Mm_Celera | 18:64895569 | TCACCCCTAAGTCTT[A/G]CTTGCTAAACAGATT | 83814 |
rs30105107 | snp | A/G | 0.375 | 0.216506 | intron-variant | Nedd4l | GRCm38.p3 | 18:65038941 | AATGCATAGAAGTGT[A/G]AGGCAACCATTGATC | 83814 |
rs30105215 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Nedd4l | GRCm38.p3 | 18:64897220 | TTAAAGGGTCGAAGC[A/G]TTCGGAAGGTTGAGA | 83814 |
rs30107884 | snp | C/T | 0.5 | 0 | intron-variant, utr-variant-5-prime | Nedd4l | GRCm38.p3 | 18:65023566 | GAGCTTGAGTTGTTC[C/T]CTAGGTCTCTGGAAT | 83814 |
rs30107913 | snp | A/G | 0.32 | 0.24 | intron-variant | Nedd4l | GRCm38.p3 | 18:64934885 | ATACACATATATTTC[A/G]AATATTTAAAAGGTA | 83814 |
rs30108190 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Nedd4l | Mm_Celera | 18:65094380 | CGGGAGCTTAAAGCA[A/G]TCAGTCACATCATCA | 83814 |
rs30108222 | snp | C/T | 0.33241 | 0.236027 | intron-variant | Nedd4l | Mm_Celera | 18:65098401 | ATCTCCTTTCTGGCT[C/T]GCTCTTTGTCTGCAT | 83814 |
rs30108624 | snp | A/T | 0.48 | 0.0979796 | utr-variant-3-prime, nc-transcript-variant | Nedd4l | Mm_Celera | 18:65213514 | ATAATATTTTTTCCA[A/T]ACTCAGAATGAAAAT | 83814 |
rs30111040 | snp | A/G | 0.375 | 0.216506 | intron-variant | Nedd4l | Mm_Celera | 18:65030082 | GCCCAGACTTTGCCT[A/G]GAAAGGACCCCTTCT | 83814 |
rs30111855 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Nedd4l | GRCm38.p3 | 18:64912429 | GTTCAGAATCCAGGT[C/T]CTTATGTTTGCATAG | 83814 |
rs30111870 | snp | C/T | 0.432133 | 0.171253 | intron-variant | Nedd4l | Mm_Celera | 18:65100214 | AGGAAGTTCCATGGA[C/T]GTATGTGTGTGTGTG | 83814 |
rs30112851 | snp | A/G/T | 0.486111 | 0.0821678 | intron-variant | Nedd4l | GRCm38.p3 | 18:64892111 | CCTCTCCTGTGTGGC[A/G/T]GTGTCTGCAGTTACC | 83814 |
rs30113126 | snp | C/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | Nedd4l, A330084C13Rik | Mm_Celera | 18:64889794 | TTGAAAGAAATATTT[C/T]GAGACTGTTTTTGGA | 83814 |
rs30113561 | snp | A/C | 0.5 | 0 | intron-variant | Nedd4l | Mm_Celera | 18:65189535 | GTGGCTGTCTATGTA[A/C]TAGCAAGTGTTGAAA | 83814 |
rs30113867 | snp | A/C | 0.459184 | 0.136902 | intron-variant, utr-variant-5-prime | Nedd4l | GRCm38.p3 | 18:65076041 | CTGTTTTCAAACAGA[A/C]GCCAGTGCACAGATT | 83814 |
rs30114368 | snp | C/T | 0.475309 | 0.108333 | intron-variant | Nedd4l | GRCm38.p3 | 18:65127989 | TCTTCATGAATGTCA[C/T]ACGTCATAGTGTAGG | 83814 |
rs30114422 | snp | A/T | 0.5 | 0 | intron-variant | Nedd4l | GRCm38.p3 | 18:64906625 | GTGCATAGCCAGTGG[A/T]GTTTAAAGGTTTTTT | 83814 |
rs30115490 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Nedd4l | GRCm38.p3 | 18:65088549 | ACAGGACAACAAATG[C/T]TGATGGCGTATGAGG | 83814 |
rs30116534 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Nedd4l | GRCm38.p3 | 18:64940684 | CTGTGGTGTGAGGCT[A/G]TGGTGGTGGGAGAGG | 83814 |
rs30117274 | snp | A/G | 0.459184 | 0.136902 | intron-variant | Nedd4l | GRCm38.p3 | 18:65196482 | CGCTCACAGGGCCCC[A/G]TGCTTGCTGCTTACC | 83814 |
rs30117566 | snp | A/G | 0.345679 | 0.230967 | intron-variant | Nedd4l | GRCm38.p3 | 18:65193740 | GATACAAAGGCCAAT[A/G]CCCTGCTCCCATAGT | 83814 |
rs30117747 | snp | A/G | 0.492188 | 0.0620098 | intron-variant | Nedd4l | Mm_Celera | 18:65183194 | ATGTGCCCAGAAGCC[A/G]AGCCATCAGCCAGTG | 83814 |
rs30118252 | snp | A/G | 0.5 | 0 | intron-variant | Nedd4l | GRCm38.p3 | 18:65055427 | GGGACTTGCCTCTCT[A/G]CCTGCAGGGAACTTT | 83814 |
rs30118835 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Nedd4l | GRCm38.p3 | 18:65029396 | AAACTACTCCAGCCC[A/C]CTTCTGGTAGACATG | 83814 |
rs30119019 | snp | A/G | 0.375 | 0.216506 | intron-variant | Nedd4l | Mm_Celera | 18:65002203 | TGTGTGCGCGCGTGT[A/G]TGTGTGTGTGTGTGT | 83814 |
rs30121372 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Nedd4l | GRCm38.p3 | 18:64931046 | CTTGATCTAATATCC[A/G]AAGAGCTATAGTCTA | 83814 |
rs30121960 | snp | A/G | 0.465374 | 0.126941 | intron-variant | Nedd4l | Mm_Celera | 18:65064533 | TAGCTTATCAAAATC[A/G]GCAAACTTACTATTT | 83814 |
rs30122244 | snp | A/G | 0.492188 | 0.0620098 | intron-variant | Nedd4l | Mm_Celera | 18:65164147 | TAAGACCACACGCAC[A/G]TGCCATGTTTCTCAA | 83814 |
rs30122316 | snp | A/G | 0.473373 | 0.11227 | intron-variant | Nedd4l | Mm_Celera | 18:65064795 | GTTCCTCGGTTCCTC[A/G]GCAGCCCTTGAGGAG | 83814 |
rs30123398 | snp | A/G | 0.429688 | 0.173817 | intron-variant | Nedd4l | Mm_Celera | 18:65072414 | ATGTTCTATTAAGGT[A/G]AGGCTTAGCTACTCT | 83814 |
rs30124426 | snp | G/T | 0.5 | 0 | intron-variant | Nedd4l | GRCm38.p3 | 18:65000457 | TCTGTATTTTGGATG[G/T]GATCATAGGGTGGCT | 83814 |
rs30127394 | snp | G/T | 0.5 | 0 | intron-variant | Nedd4l | Mm_Celera | 18:65189454 | TGTCTGAGGTGGAGT[G/T]TAGTGCTGAGAGAAT | 83814 |
rs30128081 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Nedd4l | GRCm38.p3 | 18:64973665 | GGAGGAGAAGGCCGA[C/T]AGCAGAGGACCCTGG | 83814 |
rs30130007 | snp | A/T | 0.5 | 0 | intron-variant | Nedd4l | GRCm38.p3 | 18:65133695 | CTCTCCCTCCTATAG[A/T]TTCCCAGGTTCTTGC | 83814 |
rs30130027 | snp | C/T | 0.375 | 0.216506 | intron-variant | Nedd4l | GRCm38.p3 | 18:64969561 | GGGCTTCATCTATAG[C/T]TGCCTTTGACCTCAT | 83814 |
rs30150576 | snp | C/T | 0.375 | 0.216506 | intron-variant | Nedd4l | GRCm38.p3 | 18:65067861 | GCTCTCAGGAATTCC[C/T]TTGACCCAGGTCTGG | 83814 |
rs30151376 | snp | A/T | 0.32 | 0.24 | intron-variant | Nedd4l | GRCm38.p3 | 18:64934953 | TAATTACACAATGCA[A/T]GTGTGTGTAGAATAG | 83814 |
rs30153032 | snp | C/T | 0.475309 | 0.108333 | intron-variant | Nedd4l | Mm_Celera | 18:65175693 | GTGGGCCAAGAGAGC[C/T]GCTCTTTGGCAAGTA | 83814 |
rs30154381 | snp | G/T | 0.375 | 0.216506 | intron-variant | Nedd4l | GRCm38.p3 | 18:65126869 | AGGGTTTTTGATGAG[G/T]TATCTTGACAGCAAG | 83814 |
rs30155398 | snp | G/T | 0.429688 | 0.173817 | intron-variant | Nedd4l | GRCm38.p3 | 18:65110001 | ACTCGGGATGCTGAG[G/T]GTCCCCAGGGAGCAG | 83814 |
rs30155409 | snp | G/T | 0.493827 | 0.0552116 | intron-variant | Nedd4l | Mm_Celera | 18:65182966 | CCATCTATCTCCCTT[G/T]GCTACCACCATGCCC | 83814 |
rs30160718 | snp | A/C | 0.336735 | 0.234472 | intron-variant | Nedd4l | GRCm38.p3 | 18:64934716 | GACTGAAGGCGTTGG[A/C]TACAAGACTGCCTCT | 83814 |
rs30161712 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Nedd4l | GRCm38.p3 | 18:65069392 | CTTCATAGCTGGCAG[A/G]CAAGGTAGTGACTTG | 83814 |
rs30162443 | snp | A/G | 0.32 | 0.24 | intron-variant | Nedd4l | GRCm38.p3 | 18:65056929 | CACTCCAAGTCATGG[A/G]AACCAAGCCAGCCAC | 83814 |
rs30162646 | snp | A/G | 0.5 | 0 | intron-variant, upstream-variant-2KB | Nedd4l | Mm_Celera | 18:65074002 | CACTGGTACCTTTCT[A/G]ATGAGCCATCTGACT | 83814 |
rs30163585 | snp | A/T | 0.495868 | 0.0452663 | intron-variant | Nedd4l | GRCm38.p3 | 18:65031703 | GAGAATTGCATGTAT[A/T]TGTGAGCTTTGGTCA | 83814 |
rs30164134 | snp | A/G | 0.33241 | 0.236027 | intron-variant | Nedd4l | GRCm38.p3 | 18:65095241 | AGCCGCATTTTCTGG[A/G]AGCAGAGTTTGGAAC | 83814 |
rs30165117 | snp | C/G | 0.5 | 0 | intron-variant | Nedd4l | Mm_Celera | 18:65063483 | TTTACATTGATTTCT[C/G]TCTGTGTGTGTGTGT | 83814 |
rs30165833 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Nedd4l | Mm_Celera | 18:64934297 | TCTGGAAGTTGCTTT[G/T]CTTTGTAACCCCCAC | 83814 |
rs30165973 | snp | A/G | 0.5 | 0 | intron-variant | Nedd4l | GRCm38.p3 | 18:65109446 | TGATGCTGCACAACC[A/G]ACTTCATGACTAACT | 83814 |
rs30166911 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Nedd4l | GRCm38.p3 | 18:65200505 | CAGTCCTGCCTGTCT[C/T]CTTTGATTCTCTGCA | 83814 |
rs30167235 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Nedd4l | GRCm38.p3 | 18:65004764 | CTTTTAAACTTGGAA[C/T]ACCTGCTCTTCTTCA | 83814 |
rs30168632 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Nedd4l | Mm_Celera | 18:65037880 | ATGGACCTCCACCGT[A/G]CACATGTAAACAGCG | 83814 |
rs30168817 | snp | C/T | 0.33241 | 0.236027 | intron-variant | Nedd4l | Mm_Celera | 18:65083130 | ACTCATTCTCCGATA[C/T]GGTGGGGAGGTGGAT | 83814 |
rs30170304 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Nedd4l | GRCm38.p3 | 18:65206263 | CTGCTACTGTGCTTC[C/T]AAAAATTGTGCTCTC | 83814 |
rs30170629 | snp | A/G | 0.432133 | 0.171253 | intron-variant | Nedd4l | Mm_Celera | 18:65097188 | CTGTAAGAAGGAGGT[A/G]GAATTGGGGTTCTAA | 83814 |
rs30172148 | snp | C/T | 0.465374 | 0.126941 | intron-variant | Nedd4l | Mm_Celera | 18:65124446 | TTTAATGTCAGGAAA[C/T]CTTTCATACGTTGGT | 83814 |
rs30173965 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Nedd4l | GRCm38.p3 | 18:65088698 | CTGGGGTTCTTTTTG[C/T]TTGTTCTTAATCTTG | 83814 |
rs30175551 | snp | C/T | 0.456747 | 0.140554 | intron-variant | Nedd4l | GRCm38.p3 | 18:65003050 | GTTGTCCCTGGTCTA[C/T]AGTGAGTCGCTGAGT | 83814 |
rs30176008 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Nedd4l | GRCm38.p3 | 18:64940399 | CTCCAAGCACAGTTG[A/C]AGTCAGAGGTTCTGA | 83814 |
rs30176800 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Nedd4l | Mm_Celera | 18:65106145 | CAGGGACTGCCTGTG[A/G]CCTAAGGAGCACCAG | 83814 |
rs30177555 | snp | C/T | 0.35503 | 0.226867 | intron-variant | Nedd4l | GRCm38.p3 | 18:64980780 | CCCTGCAAATTAGAT[C/T]ATAGATACAACCTCT | 83814 |
rs30180465 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Nedd4l | GRCm38.p3 | 18:65012379 | CTAATACTTAAACCT[A/C]CGCAGGCCATTCTCA | 83814 |
rs30195080 | snp | C/T | 0.492188 | 0.0620098 | intron-variant | Nedd4l | GRCm38.p3 | 18:65041601 | ATGCGGGTAAGACAG[C/T]GGGGCATATGTTAAG | 83814 |
rs30196215 | snp | C/T | 0.375 | 0.216506 | intron-variant | Nedd4l | GRCm38.p3 | 18:65055171 | TTGGCTTGTTGTGTT[C/T]ATACGGATCTATATT | 83814 |
rs30197147 | snp | A/T | 0.489796 | 0.070696 | intron-variant | Nedd4l | Mm_Celera | 18:65183150 | AAAGTGTTAGAGAAA[A/T]ATCTAGAAATGTTTT | 83814 |
rs30199720 | snp | C/T | 0.5 | 0 | intron-variant | Nedd4l | GRCm38.p3 | 18:65211224 | AGGGACAGACACCGC[C/T]TAGGAGATTTTATAG | 83814 |
rs30204842 | snp | A/G | 0.49827 | 0.0293608 | intron-variant | Nedd4l | GRCm38.p3 | 18:64920732 | GTGTGTTATAAACCC[A/G]GTGCTGGCGGCTCAT | 83814 |
rs30206081 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Nedd4l | GRCm38.p3 | 18:64941011 | GTAATTCCACATCCA[A/G]TCATGATTGCTGACT | 83814 |
rs30207012 | snp | A/G | 0.375 | 0.216506 | intron-variant | Nedd4l | GRCm38.p3 | 18:65041670 | AGAGAGAGTAGTAAT[A/G]GTCTCCCATCCAAGT | 83814 |
rs30207467 | snp | A/G | 0.492188 | 0.0620098 | intron-variant | Nedd4l | GRCm38.p3 | 18:64986839 | CCGATCACCACCACA[A/G]AGCTTTTCTGATGCA | 83814 |
rs30208133 | snp | A/C | 0.5 | 0 | intron-variant | Nedd4l | GRCm38.p3 | 18:65134667 | TGTTCTCTTTGTTTC[A/C]CGTTGGCCCTTCATT | 83814 |
rs30208596 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Nedd4l | GRCm38.p3 | 18:65012371 | CAAACATTCTAATAC[A/T]TAAACCTACGCAGGC | 83814 |
rs30209465 | snp | C/T | 0.5 | 0 | intron-variant | Nedd4l | GRCm38.p3 | 18:65211123 | TGAGTGACCCATGAG[C/T]TGTGGCACCATCATG | 83814 |
rs30210376 | snp | C/T | 0.32 | 0.24 | intron-variant | Nedd4l | GRCm38.p3 | 18:64890784 | GAGTGACAGTGATTG[C/T]GATGTTAGCTTTGCC | 83814 |
rs30211395 | snp | G/T | 0.498615 | 0.0262793 | intron-variant, upstream-variant-2KB | Nedd4l | Mm_Celera | 18:65074101 | CAGAATCAGTGCATC[G/T]GAGTGTATCGGCACT | 83814 |
rs30213528 | snp | C/T | 0.498615 | 0.0262793 | intron-variant | Nedd4l | GRCm38.p3 | 18:64917340 | TTTAGTGGTGTTGTA[C/T]AGGATTCCCAGAGGT | 83814 |
rs30213957 | snp | G/T | 0.415225 | 0.187619 | intron-variant | Nedd4l | GRCm38.p3 | 18:64995186 | AGGGTCATTCCACAC[G/T]TCTCCTCTTGCTGCC | 83814 |
rs30214207 | snp | G/T | 0.465374 | 0.126941 | intron-variant | Nedd4l | GRCm38.p3 | 18:65056846 | GAGTCATAAGTGGCA[G/T]AGTTGAGTGTAAACC | 83814 |
rs30214367 | snp | A/G | 0.495 | 0.0497494 | intron-variant | Nedd4l | GRCm38.p3 | 18:64981775 | CTCCCAAACGCTGTA[A/G]ACGTAGACTAGTATT | 83814 |
rs30214479 | snp | C/T | 0.359862 | 0.224567 | intron-variant | Nedd4l | Mm_Celera | 18:65099939 | AGAAGGAAATTAATA[C/T]TTACTTCAGCCTCCA | 83814 |
rs30215383 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Nedd4l | GRCm38.p3 | 18:64931124 | TTGCAGGCACACTTT[A/C]CTGGCGATCCCCTGG | 83814 |
rs30215470 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Nedd4l | Mm_Celera | 18:65182949 | TTATCTGGCAAAATC[A/C]ACCATCTATCTCCCT | 83814 |
rs30215898 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Nedd4l | GRCm38.p3 | 18:65070508 | AGTAGCGAGGACTCA[C/T]ATATTCCAGGCTGAC | 83814 |
rs30216695 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Nedd4l | GRCm38.p3 | 18:64925879 | CTTGGTGGGCTCATG[A/G]CTTGGCTCATGGCCA | 83814 |
rs30217220 | snp | C/T | 0.375 | 0.216506 | intron-variant | Nedd4l | Mm_Celera | 18:65044230 | TGGTTGTTAATTTTT[C/T]ATTGGTTTTTTGGAC | 83814 |
rs30221745 | snp | A/C | 0.375 | 0.216506 | intron-variant | Nedd4l | GRCm38.p3 | 18:64921863 | GGTAATGTCATTTAC[A/C]ATTTGATGCTGACTA | 83814 |
rs30224396 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Nedd4l | Mm_Celera | 18:65037890 | ACCGTACACATGTAA[A/G]CAGCGCTAGATGAAT | 83814 |
rs30225018 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Nedd4l | Mm_Celera | 18:65158855 | ACGAGTGATAGTCTA[A/G]TCTCTTCAACCCAAG | 83814 |
rs30225857 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Nedd4l | GRCm38.p3 | 18:65088682 | TTATATTCAGTGGAG[A/G]CTGGGGTTCTTTTTG | 83814 |
rs30226930 | snp | C/T | 0.5 | 0 | intron-variant | Nedd4l | GRCm38.p3 | 18:65032107 | AGAGGGAGTCAGGCC[C/T]CAGGCCCAGGTTCAG | 83814 |
rs30227930 | snp | C/T | 0.375 | 0.216506 | intron-variant | Nedd4l | GRCm38.p3 | 18:64965247 | TTCAAAAGCTGGGAG[C/T]GCAGGGGTAAGGGGC | 83814 |
rs30228070 | snp | C/T | 0.387812 | 0.208586 | intron-variant | Nedd4l | GRCm38.p3 | 18:65003477 | GTTAAAAGGTACAGT[C/T]TTGTATCTTGCAGAG | 83814 |
rs30250307 | snp | A/G | 0.387812 | 0.208586 | intron-variant | Nedd4l | GRCm38.p3 | 18:65085148 | TGATGTTGGTAGTGC[A/G]TTTGAAACCCTGCTT | 83814 |
rs30250378 | snp | A/G | 0.375 | 0.216506 | intron-variant, upstream-variant-2KB | Nedd4l | GRCm38.p3 | 18:65023430 | CACTCATTGTAAAGG[A/G]GGGCATTCCAAATAG | 83814 |
rs30252371 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Nedd4l | GRCm38.p3 | 18:64912522 | TCTTAGTCAGGGTTT[C/T]TATTCCTGCACAAAC | 83814 |
rs30255621 | snp | A/G | 0.32 | 0.24 | intron-variant | Nedd4l | Mm_Celera | 18:64980081 | ACTTTATTATGATGA[A/G]CTATCTCCCTTGTAT | 83814 |
rs30256715 | snp | A/G | 0.265928 | 0.249492 | intron-variant | Nedd4l | GRCm38.p3 | 18:65077468 | CGGGTGAGCTCATTC[A/G]TGGTTTATGGTTTCA | 83814 |
rs30256861 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Nedd4l | GRCm38.p3 | 18:65107031 | ATACATGCCAGATGA[A/G]CATGGCAGCCCATTT | 83814 |
rs30257277 | snp | A/G | 0.48 | 0.0979796 | utr-variant-3-prime, nc-transcript-variant | Nedd4l | Mm_Celera | 18:65213571 | TTTTGTACAAATTTA[A/G]ATACTAAGTCCAGGC | 83814 |
rs30257280 | snp | C/T | 0.290657 | 0.246672 | intron-variant | Nedd4l | Mm_Celera | 18:65202431 | TACCAGCTTAATTGA[C/T]TCTTAATAAAAATAA | 83814 |
rs30258023 | snp | C/T | 0.49827 | 0.0293608 | intron-variant | Nedd4l | GRCm38.p3 | 18:65030213 | TCTTTACTGTGTGCG[C/T]CCCCATAGAATCCAC | 83814 |
rs30258258 | snp | A/T | 0.432133 | 0.171253 | intron-variant | Nedd4l | Mm_Celera | 18:65095341 | GACTTGAGGGTGGGC[A/T]CCCAAGCACAGTGTG | 83814 |
rs30260317 | snp | G/T | 0.33241 | 0.236027 | intron-variant | Nedd4l | Mm_Celera | 18:65099572 | ATTAGTTGCTAATTT[G/T]GGGTGCGCTTGAAAC | 83814 |
rs30260748 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Nedd4l | GRCm38.p3 | 18:65031590 | GGCGGGGTTATCACC[C/T]GGTGATGCCAACCAA | 83814 |
rs30260887 | snp | C/G/T | 0.432133 | 0.171253 | intron-variant | Nedd4l | Mm_Celera | 18:65098222 | TCAGAGCAGTGGCCC[C/G/T]GTGTAATTTGCTGCT | 83814 |
rs30261671 | snp | A/T | 0.48 | 0.0979796 | intron-variant, upstream-variant-2KB | Nedd4l | Mm_Celera | 18:65074114 | TCGGAGTGTATCGGC[A/T]CTATCAGTAGACAGT | 83814 |
rs30261865 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Nedd4l | Mm_Celera | 18:65086558 | TGGTTGGCAAACTGA[C/T]GCTTTTCTTTTAAGC | 83814 |
rs30261915 | snp | A/G | 0.375 | 0.216506 | intron-variant | Nedd4l | GRCm38.p3 | 18:65188421 | ACTTTCAGTGTGTGT[A/G]TTCAATTGAAATAAC | 83814 |
rs30262558 | snp | G/T | 0.5 | 0 | utr-variant-3-prime, nc-transcript-variant | Nedd4l | GRCm38.p3 | 18:65214025 | TGCGGTATCTATCAG[G/T]TGTGAACTTGGCTGC | 83814 |
rs30262717 | snp | A/G | 0.5 | 0 | intron-variant | Nedd4l | GRCm38.p3 | 18:65211197 | TGAGAAGAGCCACAC[A/G]ACACCCAGGACAGGG | 83814 |
rs30262869 | snp | G/T | 0.42 | 0.183303 | intron-variant | Nedd4l | GRCm38.p3 | 18:64986216 | TCTCCTGCTGTGTAC[G/T]GCTATGAACATCCCT | 83814 |
rs30264456 | snp | C/G | 0.375 | 0.216506 | intron-variant, upstream-variant-2KB | Nedd4l, A330084C13Rik | GRCm38.p3 | 18:64889852 | TGTCATGGTCCGTCC[C/G]GGCTTTGTTTATGAT | 83814 |
rs30265086 | snp | A/T | 0.492188 | 0.0620098 | intron-variant | Nedd4l | GRCm38.p3 | 18:65038849 | AGTTTCTAAAGCGAG[A/T]AAGAATTGTCAAGGG | 83814 |
rs30265775 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Nedd4l | GRCm38.p3 | 18:65037167 | AAGTCCTTTAAAACA[A/G]AGTGAGAAAGGTGTG | 83814 |
rs30266230 | snp | C/G | 0.32 | 0.24 | intron-variant | Nedd4l | GRCm38.p3 | 18:64934820 | CAAATACAGTGTGTG[C/G]TATACACAGATCTCA | 83814 |
rs30266786 | snp | C/T | 0.265928 | 0.249492 | intron-variant | Nedd4l | GRCm38.p3 | 18:65101922 | AAGTGTTCTTAGCCA[C/T]AGTCTGTGCTGGGTC | 83814 |
rs30267518 | snp | C/G | 0.475309 | 0.108333 | intron-variant | Nedd4l | Mm_Celera | 18:65179876 | GTGAAAGAGTGCTTG[C/G]GGCACGAGCGTTAGG | 83814 |
rs30267641 | snp | A/G | 0.456747 | 0.140554 | intron-variant | Nedd4l | GRCm38.p3 | 18:65057447 | CACCTTACTGCGTGA[A/G]TACAATGGCATTGCC | 83814 |
rs30267807 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Nedd4l | Mm_Celera | 18:65038045 | ACCAGCACCACGCCC[A/G]GCAAGCACTGGTAGG | 83814 |
rs30267889 | snp | G/T | 0.375 | 0.216506 | intron-variant | Nedd4l | GRCm38.p3 | 18:65041246 | AGAATGTGAGGGAAG[G/T]ATGCTGAGAAAGGTT | 83814 |
rs30268605 | snp | A/C | 0.290657 | 0.246672 | intron-variant | Nedd4l | Mm_Celera | 18:65124201 | AGCAGTAAGAAGAAA[A/C]CTCTGTGTACAAATG | 83814 |
rs30269736 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Nedd4l | GRCm38.p3 | 18:64983218 | TTGGCCCATTACCCA[G/T]TCCGATGAGAGCCTT | 83814 |
rs30269828 | snp | A/G | 0.387812 | 0.208586 | intron-variant | Nedd4l | GRCm38.p3 | 18:65096992 | CTTCATCACTCTCAA[A/G]TCTGCCTGCCAAGTG | 83814 |
rs30271182 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Nedd4l | GRCm38.p3 | 18:65036200 | TACTGGCTTGTTTGG[A/G]GAATGCCAGCTATGT | 83814 |
rs30271375 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Nedd4l | Mm_Celera | 18:65129647 | TGGGCATCAGGCATG[C/T]GTGTGGTGTAGAGAT | 83814 |
rs30271443 | snp | C/T | 0.33241 | 0.236027 | intron-variant | Nedd4l | GRCm38.p3 | 18:65071939 | GCACTGTGCTGGCCA[C/T]TACTGGTGCTCAGCA | 83814 |
rs30271525 | snp | A/G | 0.465374 | 0.126941 | intron-variant | Nedd4l | Mm_Celera | 18:65173534 | TGACATGCTTTAGTG[A/G]CCGCCCTGAACGTCA | 83814 |
rs30272320 | snp | C/T | 0.375 | 0.216506 | intron-variant | Nedd4l | GRCm38.p3 | 18:65127864 | CTACAGAGCAAGTTC[C/T]AATACATCCAGGGAA | 83814 |
rs30272649 | snp | A/G | 0.5 | 0 | intron-variant | Nedd4l | GRCm38.p3 | 18:64986634 | AGGTTAGCCACTTTG[A/G]ATGCCAGGCTCCGCT | 83814 |
rs30273308 | snp | A/T | 0.473373 | 0.11227 | intron-variant | Nedd4l | GRCm38.p3 | 18:64932384 | TCTTCCTCAGGGTGG[A/T]AGATGGTTGCTTCGG | 83814 |
rs30273736 | snp | C/T | 0.32 | 0.24 | intron-variant | Nedd4l | Mm_Celera | 18:64968701 | ATATACTTTTCTAAA[C/T]ATTAACCTTTAAAAT | 83814 |
rs30273737 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Nedd4l | GRCm38.p3 | 18:65134118 | AAATCTCTCTTTTCC[A/G]TGTTTCTTTCCTGAC | 83814 |
rs30274137 | snp | C/T | 0.456747 | 0.140554 | intron-variant | Nedd4l | GRCm38.p3 | 18:64988241 | GAAGGAAGAAAAGAA[C/T]GCCAAGGAACCTCAG | 83814 |
rs30276674 | snp | A/T | 0.497778 | 0.0332592 | intron-variant | Nedd4l | GRCm38.p3 | 18:65058179 | GCTATACTGATGGAT[A/T]TGGGCATGGTGTCTT | 83814 |
rs30276937 | snp | C/T | 0.297521 | 0.245442 | intron-variant | Nedd4l | GRCm38.p3 | 18:64928352 | GAAGAAACAGAAAAC[C/T]TAAAATAAATCCATG | 83814 |
rs30278629 | snp | A/G | 0.375 | 0.216506 | intron-variant | Nedd4l | GRCm38.p3 | 18:64936325 | TTGTCACACACGTAA[A/G]TACAGCTTAAACAAA | 83814 |
rs30299130 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Nedd4l | Mm_Celera | 18:65073530 | GATCTTGAAGTATTT[C/T]CTGTAGTCTTTGCGA | 83814 |
rs30300509 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Nedd4l | Mm_Celera | 18:65162696 | GGCAAAGGCCCTTGT[C/T]GTCCTTGTGCTGATC | 83814 |
rs30300589 | snp | C/T | 0.375 | 0.216506 | intron-variant | Nedd4l | GRCm38.p3 | 18:65006000 | CAGATGATTGTGAGC[C/T]ACCATGTGGTTGCTG | 83814 |
rs30301372 | snp | C/T | 0.5 | 0 | intron-variant | Nedd4l | GRCm38.p3 | 18:65133692 | AGCCTCTCCCTCCTA[C/T]AGATTCCCAGGTTCT | 83814 |
rs30303221 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Nedd4l | GRCm38.p3 | 18:65126850 | ATAGGACAAGAAAAT[G/T]TCCAGGGTTTTTGAT | 83814 |
rs30304041 | snp | A/G/T | 0.415225 | 0.187619 | intron-variant | Nedd4l | Mm_Celera | 18:65098279 | GGCTCACTAAGCTTC[A/G/T]GCATGTATCGTTGTT | 83814 |
rs30305187 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Nedd4l | GRCm38.p3 | 18:65032716 | ATTTGCCCTTTCTCA[A/G]CATGATAGATGCTAT | 83814 |
rs30305322 | snp | C/G | 0.375 | 0.216506 | intron-variant | Nedd4l | GRCm38.p3 | 18:65005817 | GCTATGGCTGGAACT[C/G]AAGGCAAGAGCTTGG | 83814 |
rs30305448 | snp | C/T | 0.432133 | 0.171253 | intron-variant | Nedd4l | Mm_Celera | 18:65064453 | TAATTTTCATATTCT[C/T]TGTGATACAAGATTT | 83814 |
rs30306349 | snp | A/G | 0.375 | 0.216506 | intron-variant | Nedd4l | Mm_Celera | 18:65062818 | TTAGAACCTCTGCTC[A/G]CTCTGGTTGACGCCA | 83814 |
rs30307482 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Nedd4l | Mm_Celera | 18:65096191 | CCAGATTTTTTTTTT[C/T]TTTTTGAATCTGTGT | 83814 |
rs30309774 | snp | A/C | 0.48 | 0.0979796 | intron-variant | Nedd4l | Mm_Celera | 18:65072803 | AACCCAGCAATCTGC[A/C]TTTTAGCCACTCTCT | 83814 |
rs30863951 | snp | C/G/T | 0.5 | 0 | intron-variant | Nedd4l | GRCm38.p3 | 18:65067556 | TGTTTCTCTCTCTCT[C/G/T]TGTTTCTTTCTCTCT | 83814 |
rs33859257 | snp | A/G | 0.46875 | 0.121031 | intron-variant | Nedd4l | Mm_Celera | 18:65044489 | ATCATTGCATACCTG[A/G]GCAGCTTCTCTCTGT | 83814 |
rs33859449 | snp | C/T | 0.492188 | 0.0620098 | intron-variant | Nedd4l | Mm_Celera | 18:65167035 | ACTGTGCCGCGCTGT[C/T]GGGGATCCTTCTCAG | 83814 |
rs36245490 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Nedd4l | Mm_Celera | 18:64926644 | AGCAATGGCCCTTTT[C/G]TCCTGGAAGTTGTGA | 83814 |
rs36245742 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Nedd4l | Mm_Celera | 18:64925221 | ATCAGTTATCCAAGC[C/T]CTGTGTTCTTCCACA | 83814 |
rs36248285 | snp | A/G | 0.197531 | 0.244432 | intron-variant | Nedd4l | Mm_Celera | 18:64935453 | CACCTGCTGATTACA[A/G]TAGAGACTGATCTGT | 83814 |
rs36250116 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Nedd4l | Mm_Celera | 18:65044477 | ATCAACTACAGCATC[A/G]TTGCATACCTGAGCA | 83814 |
rs36260980 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Nedd4l | Mm_Celera | 18:65000044 | ACCTATAAATTTCAG[C/T]TCTCAGTTTTCCTAT | 83814 |
rs36261421 | snp | C/T | 0.459184 | 0.136902 | intron-variant, utr-variant-5-prime | Nedd4l | GRCm38.p3 | 18:64976852 | GGAAAGTTACCAAGC[C/T]GCAGGCCAGCCTGGT | 83814 |
rs36262986 | snp | A/C | 0.32 | 0.24 | intron-variant | Nedd4l | Mm_Celera | 18:64902228 | TAAAACAAAATTTTT[A/C]AATGAGCCAAAATAT | 83814 |
rs36263988 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Nedd4l | Mm_Celera | 18:65045656 | AACCTTCTTTTGATA[C/T]TTTCATAAGTGCCTA | 83814 |
rs36264544 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Nedd4l | Mm_Celera | 18:64961097 | AAGGAGCAAAACTCA[C/T]ACACGTCGGAAGGTG | 83814 |
rs36265271 | snp | A/G | 0.489796 | 0.070696 | intron-variant | Nedd4l | GRCm38.p3 | 18:64946348 | CTCACAGAGAATAAT[A/G]GTGATAGAAATCGAA | 83814 |
rs36266170 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Nedd4l | Mm_Celera | 18:65016655 | TTTCATTCCAGGATT[C/T]GCAGCTGAGCTATTT | 83814 |
rs36269702 | snp | A/G | 0.32 | 0.24 | intron-variant | Nedd4l | Mm_Celera | 18:65061975 | CTTATGTGCACTTCC[A/G]AAGGCCATAAAGTCC | 83814 |
rs36272532 | snp | C/T | 0.495868 | 0.0452663 | intron-variant | Nedd4l | GRCm38.p3 | 18:64926964 | CTCCTCTCATTCATA[C/T]ACCCTCAACCTCTGC | 83814 |
rs36277021 | snp | A/G | 0.375 | 0.216506 | intron-variant | Nedd4l | Mm_Celera | 18:65044810 | TTGAGATCTAAACAC[A/G]TTTCCTATTTATGTT | 83814 |
rs36279763 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Nedd4l | Mm_Celera | 18:64924288 | CACGTGAGGATGGCA[C/T]AGAATTAATGGGTAG | 83814 |
rs36280257 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Nedd4l | GRCm38.p3 | 18:64952710 | ATGGTGTAAAGAACA[C/T]TGAGTCAGGCTGAGA | 83814 |
rs36282669 | snp | A/G | 0.197531 | 0.244432 | intron-variant | Nedd4l | Mm_Celera | 18:64901293 | AAAAATGGTTTCACA[A/G]GTACTTTGGAGTCTA | 83814 |
rs36283143 | snp | A/T | 0.5 | 0 | intron-variant | Nedd4l | GRCm38.p3 | 18:64959132 | TGTTGTGTTTGAGTG[A/T]TTACATTACTTCTGC | 83814 |
rs36283368 | snp | A/T | 0.48 | 0.0979796 | intron-variant, upstream-variant-2KB | Nedd4l | Mm_Celera | 18:65074095 | GCTTAGCAGAATCAG[A/T]GCATCGGAGTGTATC | 83814 |
rs36286234 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Nedd4l | Mm_Celera | 18:64988279 | ATAAATATTTCCTAC[A/C]GTGTGTGAAGGCAGA | 83814 |
rs36286974 | snp | C/G | 0.244898 | 0.249948 | intron-variant | Nedd4l | Mm_Celera | 18:65000732 | GCAGCACGTGTTGTT[C/G]CTAATGTACTGACAT | 83814 |
rs36288729 | snp | A/T | 0.459184 | 0.136902 | intron-variant, upstream-variant-2KB | Nedd4l | Mm_Celera | 18:65075134 | GCAAAAGAGAAATGG[A/T]TTGATTTGAAATAAC | 83814 |
rs36291824 | snp | C/G | 0.197531 | 0.244432 | intron-variant | Nedd4l | Mm_Celera | 18:64938398 | AAGAAAGCAACACTT[C/G]GAATACAAGGAAATC | 83814 |
rs36293427 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Nedd4l | Mm_Celera | 18:64953160 | ATTCACCAGATGCAC[C/T]TCTCCTCCTTGAGCC | 83814 |
rs36293851 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Nedd4l | Mm_Celera | 18:65071781 | AACCCTTTGTGGCAA[A/G]TCAGCATCACCTCAG | 83814 |
rs36294970 | snp | C/T | 0.21875 | 0.248039 | intron-variant | Nedd4l | GRCm38.p3 | 18:64951148 | AGCATATCAGAACCA[C/T]GCAGGTGGGCTTGGA | 83814 |
rs36295699 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Nedd4l | Mm_Celera | 18:64998387 | TTGAACCTGGTGTGG[C/T]TGACGTGTATAATCT | 83814 |
rs36296505 | snp | C/T | 0.18 | 0.24 | intron-variant | Nedd4l | Mm_Celera | 18:64937890 | TACCAATTCACTCAA[C/T]GACCGTGTCTTGTTT | 83814 |
rs36297345 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Nedd4l | Mm_Celera | 18:64981527 | CCACTGCAGTGCTTC[C/T]CGTGGCCAGGATGAT | 83814 |
rs36299140 | snp | C/T | 0.459184 | 0.136902 | intron-variant | Nedd4l | GRCm38.p3 | 18:65008188 | TTTCCTTGCTAGGTT[C/T]CTGGCCTCTGTGAGC | 83814 |
rs36300048 | snp | C/T | 0.297521 | 0.245442 | intron-variant, upstream-variant-2KB | Nedd4l | Mm_Celera | 18:65021696 | AGACATGGTTAGGAA[C/T]GTTGCTTTAAATGTG | 83814 |
rs36304580 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Nedd4l | GRCm38.p3 | 18:65034995 | TCCACTTCTGAGACT[C/T]GCCGCAGGAAGCTAA | 83814 |
rs36306893 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Nedd4l | Mm_Celera | 18:64933782 | GCTAGGTGCTCATGG[A/G]AAAGTGAGTAAAATT | 83814 |
rs36307712 | snp | A/T | 0.459184 | 0.136902 | intron-variant | Nedd4l | Mm_Celera | 18:65009807 | TGGGATAGGCTACTG[A/T]TTTTCCTCTAGCACT | 83814 |
rs36313613 | snp | A/T | 0.297521 | 0.245442 | intron-variant | Nedd4l | Mm_Celera | 18:65015632 | GGCCATTCATCCCTG[A/T]GGTCCACAGCATCAG | 83814 |
rs36316891 | snp | A/G | 0.408163 | 0.193609 | intron-variant, upstream-variant-2KB | Nedd4l | GRCm38.p3 | 18:65024868 | GTAAGCTGTCTTTCC[A/G]TGCGATCATTTGCAA | 83814 |
rs36318329 | snp | A/G | 0.375 | 0.216506 | intron-variant | Nedd4l | GRCm38.p3 | 18:64959533 | GTCATGGAGAACAGT[A/G]CTCGGCAGCTGTGGT | 83814 |
rs36321985 | snp | A/G | 0.124444 | 0.216185 | intron-variant, utr-variant-5-prime | Nedd4l | GRCm38.p3 | 18:64976837 | GGCACCACCACAGGA[A/G]GAAAGTTACCAAGCT | 83814 |
rs36322122 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Nedd4l | Mm_Celera | 18:65032005 | ATCAGATGCAAATAT[C/T]CAGTGGGCTAGGAAC | 83814 |
rs36322362 | snp | C/G | 0.152778 | 0.230321 | intron-variant | Nedd4l | Mm_Celera | 18:64962395 | TCAAATGCAAACTCA[C/G]TTTGAAACTCTTTGT | 83814 |
rs36330524 | snp | A/G | 0.489796 | 0.070696 | intron-variant | Nedd4l | Mm_Celera | 18:64914068 | TTAGCCCAAGGACAT[A/G]GGATAATCACATCCA | 83814 |
rs36331043 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Nedd4l | GRCm38.p3 | 18:64918175 | AAAGAGACTGGCGAC[C/T]TTGCAAAGACAAAGA | 83814 |
rs36338641 | snp | A/G | 0.495868 | 0.0452663 | intron-variant | Nedd4l | GRCm38.p3 | 18:64931292 | AGACAGACAGACAGC[A/G]GACAGTGTGCATAGC | 83814 |
rs36343476 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Nedd4l | Mm_Celera | 18:64948984 | TGCCAAAACTTACAG[C/T]CTGGAGAAATATAGT | 83814 |
rs36343701 | snp | C/T | 0.21875 | 0.248039 | intron-variant | Nedd4l | Mm_Celera | 18:64926747 | ATGTGTTTATCAACA[C/T]GAATAGCTACTTTGA | 83814 |
rs36346832 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Nedd4l | Mm_Celera | 18:65033830 | TATAATTTGTTTCAC[A/G]TGCTAGTGAGATACA | 83814 |
rs36349149 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Nedd4l | Mm_Celera | 18:64953957 | CTATGAAAACACTTA[C/T]TGTGACCTATTGCCC | 83814 |
rs36350767 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Nedd4l | Mm_Celera | 18:65057592 | CAGTGACTTGGTGAC[A/G]CTCCTGATAGCTAAT | 83814 |
rs36354041 | snp | C/T | 0.486111 | 0.0821678 | intron-variant | Nedd4l | GRCm38.p3 | 18:65034390 | CAAAGTGCATTCAGC[C/T]GGAAAGGAAGAGATT | 83814 |
rs36355998 | snp | C/G | 0.18 | 0.24 | intron-variant | Nedd4l | Mm_Celera | 18:64936950 | ACCTCTTCATCATTC[C/G]CAGTGGTTTTTAAAA | 83814 |
rs36359435 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Nedd4l | GRCm38.p3 | 18:64949443 | ATTGTAAATCAGTGC[A/G]TGGATTAATGAGAAT | 83814 |
rs36366569 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Nedd4l | Mm_Celera | 18:64978618 | AAATCCTGTTTCAAA[A/G]ATGAATTCCTTAGGT | 83814 |
rs36370601 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Nedd4l | Mm_Celera | 18:64982849 | CCAGTCTATTTTGGA[C/T]TGTCAGTCACACCTG | 83814 |
rs36371063 | snp | A/T | 0.35503 | 0.226867 | intron-variant, utr-variant-5-prime | Nedd4l | Mm_Celera | 18:65075860 | GAGTCTGTTAGATAG[A/T]CTCACCACTTTGCCA | 83814 |
rs36371154 | snp | A/C | 0.142012 | 0.225474 | intron-variant | Nedd4l | Mm_Celera | 18:64992261 | TAGCGCTTCCATCAA[A/C]ATGATTGGTGTAATG | 83814 |
rs36375178 | snp | A/G | 0.165289 | 0.235211 | intron-variant | Nedd4l | Mm_Celera | 18:65028664 | CTCTCACACTGTGAG[A/G]ATGTAAAAAGCACAC | 83814 |
rs36381932 | snp | G/T | 0.32 | 0.24 | intron-variant | Nedd4l | Mm_Celera | 18:64986154 | TGATCATAGGAAAAT[G/T]TCCCTTGCGGACTGT | 83814 |
rs36382140 | snp | A/C | 0.277778 | 0.248452 | intron-variant, upstream-variant-2KB | Nedd4l | Mm_Celera | 18:65021659 | GAATAGTCTAGAGGC[A/C]TGAATGGACACCCAG | 83814 |
rs36385892 | snp | C/G | 0.48 | 0.0979796 | intron-variant | Nedd4l | GRCm38.p3 | 18:64945747 | ACTGTTCTGCCTTTT[C/G]CCGTTACTTCAGAGT | 83814 |
rs36389617 | snp | G/T | 0.5 | 0 | intron-variant | Nedd4l | GRCm38.p3 | 18:64957137 | CTCTCTTTCCCAACT[G/T]CAGTGGGCAGACATG | 83814 |
rs36390409 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Nedd4l | Mm_Celera | 18:64913960 | CCAAAATGCATAGTG[C/G]TGACCGAGACTCAGC | 83814 |
rs36391165 | snp | A/G | 0.375 | 0.216506 | intron-variant | Nedd4l | GRCm38.p3 | 18:65063612 | ACACCAAGTGGTGAT[A/G]GCTGGTGAATTATAA | 83814 |
rs36395386 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Nedd4l | Mm_Celera | 18:65069888 | GAGCTGGTCTCTTAG[C/T]GCAGAGGCCCACAAT | 83814 |
rs36397913 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Nedd4l | Mm_Celera | 18:65069191 | AAATAAACATGATGT[G/T]TGGCACCATGTAGTG | 83814 |
rs36404726 | snp | A/G | 0.486111 | 0.0821678 | intron-variant | Nedd4l | GRCm38.p3 | 18:64960074 | ACCTTGCCCTGCAAA[A/G]TAGATACCATTTCCC | 83814 |
rs36407220 | snp | C/T | 0.165289 | 0.235211 | intron-variant | Nedd4l | Mm_Celera | 18:65044815 | ATCTAAACACGTTTC[C/T]TATTTATGTTCCTGT | 83814 |
rs36408687 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Nedd4l | Mm_Celera | 18:64984121 | TGGCCATGAGAGGTT[A/G]CATGTGACCCCTTAT | 83814 |
rs36412618 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Nedd4l | Mm_Celera | 18:64987672 | TCCCACAGGAGCCTG[C/T]TCAAACTCCTGCAGC | 83814 |
rs36418278 | snp | G/T | 0.42 | 0.183303 | intron-variant | Nedd4l | Mm_Celera | 18:64908145 | TAGCTAAGAAATGGA[G/T]GTTTGTACAAGAAAG | 83814 |
rs36418574 | snp | C/T | 0.197531 | 0.244432 | intron-variant | Nedd4l | Mm_Celera | 18:64934778 | GGTTGAACTCTTAGC[C/T]AGTCTCAGATTAATT | 83814 |
rs36419027 | snp | A/G/T | 0.408163 | 0.193609 | intron-variant | Nedd4l | GRCm38.p3 | 18:64983513 | GAGAAGGAGTGAACC[A/G/T]GCTGGTGGAAGTCCT | 83814 |
rs36420498 | snp | A/G | 0.497041 | 0.0383476 | intron-variant | Nedd4l | GRCm38.p3 | 18:64930376 | CTACTGTCTAGTCAC[A/G]AATTACAATACACCA | 83814 |
rs36421155 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Nedd4l | Mm_Celera | 18:65068195 | GGTGGAAAGTGGCAC[A/G]TTGCAGTGTATGCTT | 83814 |
rs36421197 | snp | C/T | 0.197531 | 0.244432 | intron-variant | Nedd4l | Mm_Celera | 18:64904745 | GCTCCTTGTAGGTCA[C/T]TGTCAGCATTTTCCA | 83814 |
rs36422164 | snp | A/G | 0.497041 | 0.0383476 | intron-variant | Nedd4l | GRCm38.p3 | 18:64951412 | TGTGTGTGTGCTTCT[A/G]CAAAACTCAGCTCAC | 83814 |
rs36427427 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Nedd4l | Mm_Celera | 18:64981661 | CCCCGAAGCAATGCA[A/G]TACGAGTGTTGGTAC | 83814 |
rs36435236 | snp | C/T | 0.345679 | 0.230967 | intron-variant | Nedd4l | Mm_Celera | 18:64904590 | TCTATTTGAATCCAG[C/T]GTGGAGCTTGCAGTT | 83814 |
rs36438162 | snp | G/T | 0.396694 | 0.202437 | intron-variant | Nedd4l | Mm_Celera | 18:65064554 | CTTACTATTTTAGAG[G/T]AAAAGATATTGCTCT | 83814 |
rs36439465 | snp | G/T | 0.277778 | 0.248452 | intron-variant | Nedd4l | Mm_Celera | 18:65072053 | GGTTAAGCCCCCGCA[G/T]AATGGGAAGGGGTAC | 83814 |
rs36439768 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Nedd4l | Mm_Celera | 18:64966448 | TCATGCTAGTTATGA[C/T]GAGAGGGTAGTGTTA | 83814 |
rs36446366 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Nedd4l | Mm_Celera | 18:64949104 | TGGCCTTGATCAGGT[C/T]TCCATGTGCAGGATG | 83814 |
rs36450836 | snp | C/T | 0.32 | 0.24 | intron-variant | Nedd4l | Mm_Celera | 18:64981981 | AGGTCTGCCAACATT[C/T]GGGAATGAGGAGGGA | 83814 |
rs36452117 | snp | C/T | 0.35503 | 0.226867 | intron-variant | Nedd4l | Mm_Celera | 18:65070352 | TTTGGTTTTAGGGAC[C/T]GGTGTGAAATTTCAG | 83814 |
rs36453686 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Nedd4l | Mm_Celera | 18:64949521 | ATCCTCATTTCCATT[C/T]AGAATAATTTATGTT | 83814 |
rs36454097 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Nedd4l | Mm_Celera | 18:64918799 | AGCCGGCTCATTAAC[A/G]ACTGTTTAGCTTGCT | 83814 |
rs36457205 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Nedd4l | Mm_Celera | 18:64928743 | ATATCTGGTTCTAGG[C/T]ATCTATTCAGAAGTG | 83814 |
rs36458099 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Nedd4l | Mm_Celera | 18:64949998 | GGCCTTATCGCCTTT[G/T]ACCCTAACATGATTA | 83814 |
rs36459174 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Nedd4l | GRCm38.p3 | 18:64961928 | GCTGTGAGATCTCAG[A/G]TTCTGTTCTCAAACT | 83814 |
rs36459319 | snp | G/T | 0.444444 | 0.157135 | intron-variant, upstream-variant-2KB | Nedd4l | Mm_Celera | 18:65075171 | AAGGAAGCAAAATGC[G/T]TAGTTATGTGAAAAT | 83814 |
rs36461613 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Nedd4l | Mm_Celera | 18:64993762 | AGAGGCTTTTAGATT[C/T]TCCTCAGAAGAAAAT | 83814 |
rs36463298 | snp | C/T | 0.35503 | 0.226867 | intron-variant | Nedd4l | Mm_Celera | 18:64923199 | ACAACCTGTAGTATG[C/T]GTGCTTTGTCTCTAC | 83814 |
rs36464597 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Nedd4l | Mm_Celera | 18:65043342 | TGTAGCTTAGGATGC[C/T]ATCTTACATCTGCCC | 83814 |
rs36464786 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Nedd4l | Mm_Celera | 18:64913136 | CACAAGGCCGGAAAG[C/T]TGACGGCTGGGTTGG | 83814 |
rs36465824 | snp | G/T | 0.396694 | 0.202437 | intron-variant | Nedd4l | GRCm38.p3 | 18:65042851 | AAGAATTAGCATAGT[G/T]CTGGGTCAGATTGGC | 83814 |
rs36470365 | snp | A/T | 0.132653 | 0.220748 | intron-variant | Nedd4l | Mm_Celera | 18:64949929 | CCACTCCTCTAAATA[A/T]GTAGTTAGTATGAGT | 83814 |
rs36472247 | snp | C/G | 0.260355 | 0.249785 | intron-variant | Nedd4l | Mm_Celera | 18:64926945 | ACAGATCCTATGTAC[C/G]AGACTCCTCTCATTC | 83814 |
rs36478671 | snp | C/T | 0.165289 | 0.235211 | intron-variant | Nedd4l | Mm_Celera | 18:64953472 | GTGTCCTTAGTCACT[C/T]GTGACGCACCTGTGA | 83814 |
rs36479364 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Nedd4l | Mm_Celera | 18:64977564 | AAGGTAGTTTACTTC[A/G]CTTACATCTTGCTCC | 83814 |
rs36483880 | snp | C/T | 0.489796 | 0.070696 | intron-variant | Nedd4l | Mm_Celera | 18:65073597 | CTGAAGGCTAACTCT[C/T]TCCATGGTGTGTTGG | 83814 |
rs36487058 | snp | A/G | 0.426035 | 0.177515 | intron-variant | Nedd4l | GRCm38.p3 | 18:64955468 | CTAAACGAAGTCCTC[A/G]GTTTTGTTTCTCCTC | 83814 |
rs36488309 | snp | A/C | 0.408163 | 0.193609 | intron-variant | Nedd4l | Mm_Celera | 18:64911135 | CAATCTTTAAAAAAA[A/C]AGTCATATGGGAACT | 83814 |
rs36489147 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Nedd4l | GRCm38.p3 | 18:64948317 | GGCACATATTTGGCA[C/G]ACTCTAGGATACCCT | 83814 |
rs36490454 | snp | A/G | 0.5 | 0 | intron-variant | Nedd4l | Mm_Celera | 18:64953976 | GACCTATTGCCCAAC[A/G]TGAAATAATACCCCG | 83814 |
rs36490684 | snp | A/G | 0.336735 | 0.234472 | intron-variant, utr-variant-5-prime | Nedd4l | Mm_Celera | 18:65076014 | ACCTGACATTGAGAC[A/G]AGCAGTAAAATCTGT | 83814 |
rs36493602 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Nedd4l | Mm_Celera | 18:65043147 | TTTTTTCTTATTCCA[A/G]CATGCTCTTGAGTTG | 83814 |
rs36496948 | snp | A/G | 0.375 | 0.216506 | intron-variant | Nedd4l | GRCm38.p3 | 18:64951341 | TAGTCACTCGTGACT[A/G]TATTCCTTTGGACTT | 83814 |
rs36497597 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Nedd4l | Mm_Celera | 18:64949648 | TTGTCTTTATTTACC[A/G]GGAAGCAATCAACCA | 83814 |
rs36499092 | snp | A/G | 0.396694 | 0.202437 | intron-variant | Nedd4l | Mm_Celera | 18:64903096 | TTAGATTTGGTTACC[A/G]CTTATTAGACAAGAA | 83814 |
rs36499471 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Nedd4l | Mm_Celera | 18:65060478 | TAGGCAAGTTGTGAT[G/T]TTTCTAAATGTAATA | 83814 |
rs36500633 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Nedd4l | Mm_Celera | 18:65029096 | AGACCCAGAGAAGAC[A/G]TTTGATGACCTGATC | 83814 |
rs36501396 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Nedd4l | Mm_Celera | 18:65066975 | AAATGTGCTCTGGGA[A/G]GTAGAATGAAGAATC | 83814 |
rs36501899 | snp | C/G | 0.495868 | 0.0452663 | intron-variant | Nedd4l | GRCm38.p3 | 18:64913177 | AATGGGCTTCGTCAT[C/G]CCATAAATGGCTTTG | 83814 |
rs36502151 | snp | A/G | 0.42 | 0.183303 | intron-variant | Nedd4l | Mm_Celera | 18:64894277 | CTTTCTGCCTTGTGT[A/G]GTGTTTCAAATAGCA | 83814 |
rs36502395 | snp | C/T | 0.197531 | 0.244432 | intron-variant | Nedd4l | Mm_Celera | 18:64941265 | GCCGTGATACAATTC[C/T]TTTATTTATTTAATC | 83814 |
rs36503470 | snp | C/T | 0.396694 | 0.202437 | intron-variant | Nedd4l | GRCm38.p3 | 18:65042477 | GCCCAGCCCACATTA[C/T]GCCTCCATTGGCAGC | 83814 |
rs36503751 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Nedd4l | Mm_Celera | 18:64945989 | GTAATCAGTCTCCTT[C/T]TCCGTGATGGTGCGG | 83814 |
rs36505590 | snp | A/G | 0.426035 | 0.177515 | intron-variant | Nedd4l | GRCm38.p3 | 18:64930264 | ATGTTGCCTGATAAG[A/G]TTCAGACTCACAATC | 83814 |
rs36510602 | snp | G/T | 0.142012 | 0.225474 | intron-variant | Nedd4l | Mm_Celera | 18:65042825 | TTCATGTTCTGTAAC[G/T]CGTCCTCTTGAAGAA | 83814 |
rs36512954 | snp | G/T | 0.495868 | 0.0452663 | intron-variant | Nedd4l | Mm_Celera | 18:64914334 | GCAGCTAATCCACAC[G/T]AAAGCTCTCATTCAA | 83814 |
rs36514237 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Nedd4l | Mm_Celera | 18:64983012 | CTGGCTAGGGCAGTT[A/G]GAATGAAAGCCCTTG | 83814 |
rs36517380 | snp | A/G | 0.459184 | 0.136902 | intron-variant | Nedd4l | Mm_Celera | 18:64947582 | AATTCCTATATGCTG[A/G]TGATTGTTTTTAAAA | 83814 |
rs36518298 | snp | C/T | 0.408163 | 0.193609 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | Nedd4l | Mm_Celera | 18:65023846 | CTCGTTCCAGGCTGT[C/T]GATTGCCGGTAGGGA | 83814 |
rs36519746 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Nedd4l | Mm_Celera | 18:64982246 | TCTGGTCTTTTCCTG[C/T]AGAAAGAATGTGCTT | 83814 |
rs36523607 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Nedd4l | Mm_Celera | 18:65033024 | AAAGGAATTTCCAGC[C/T]TTCCCTTTAGCTGCA | 83814 |
rs36527083 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Nedd4l | Mm_Celera | 18:65071062 | CCCATCACCAGGCTT[A/T]ACCTCCAATCCTTCT | 83814 |
rs36528190 | snp | C/T | 0.375 | 0.216506 | intron-variant | Nedd4l | Mm_Celera | 18:64900496 | TGACAGAATGCAGAA[C/T]TGAGACACTCGGGCT | 83814 |
rs36530195 | snp | A/C | 0.32 | 0.24 | intron-variant | Nedd4l | Mm_Celera | 18:64966043 | CTGGCTTGGCCTGGG[A/C]CACACTCAGGTCTCT | 83814 |
rs36531371 | snp | A/G | 0.32 | 0.24 | intron-variant, utr-variant-5-prime | Nedd4l | Mm_Celera | 18:65023600 | CCAAGTTCCGCCTAT[A/G]GTGTTTGGCCAGGCT | 83814 |
rs36534731 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Nedd4l | Mm_Celera | 18:65071036 | TTAAACATCTAGATT[C/T]CCTGCTCAAACCCAT | 83814 |
rs36535631 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Nedd4l | Mm_Celera | 18:64963917 | CTCTCTCATTCCTAT[A/G]GCATTAGGTGACACA | 83814 |
rs36540073 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Nedd4l | GRCm38.p3 | 18:65010225 | GAGACGTATGACCCC[A/G]ATTCAAATCATGTTT | 83814 |
rs36542627 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Nedd4l | Mm_Celera | 18:65063325 | ATTTTTTTTCTCTAA[C/T]CAGGCAGGAAGCAGA | 83814 |
rs36545833 | snp | A/T | 0.277778 | 0.248452 | intron-variant, upstream-variant-2KB | Nedd4l | Mm_Celera | 18:65022290 | CATTTGCCAGGCTGA[A/T]CCCAAGCCTCTTAAA | 83814 |
rs36548455 | snp | G/T | 0.142012 | 0.225474 | intron-variant | Nedd4l | Mm_Celera | 18:64997204 | AGCCTTAGCATTGTA[G/T]AGCTGCCGTGTTGCC | 83814 |
rs36551974 | snp | G/T | 0.375 | 0.216506 | intron-variant | Nedd4l | Mm_Celera | 18:65010165 | GTTTGTGCAAGCAGA[G/T]GCAGATGTATAGCCG | 83814 |
rs36552852 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Nedd4l | Mm_Celera | 18:65072379 | ACGGAGGCGAATAAA[C/T]CACAAGTGGAAGAAT | 83814 |
rs36560599 | snp | A/G | 0.18 | 0.24 | intron-variant | Nedd4l | Mm_Celera | 18:64938102 | GATAAGCATTAGTCA[A/G]TCTGGAGGCACACTG | 83814 |
rs36560993 | snp | A/G | 0.493827 | 0.0552116 | intron-variant | Nedd4l | Mm_Celera | 18:64938725 | TTTTTTCTCTATCAG[A/G]GTTGCTCGTGTGCTC | 83814 |
rs36563650 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Nedd4l | Mm_Celera | 18:64984575 | AGGTCCTGAAACTTG[A/G]CTTTGCCACTTGCCT | 83814 |
rs36564381 | snp | A/T | 0.493827 | 0.0552116 | intron-variant | Nedd4l | GRCm38.p3 | 18:64961789 | TGCTGAACTACTGTT[A/T]TCTGTGCCTCCCTTC | 83814 |
rs36566215 | snp | C/T | 0.336735 | 0.234472 | intron-variant, upstream-variant-2KB | Nedd4l | Mm_Celera | 18:65075153 | ATTTGAAATAACTTA[C/T]GGAAGGAAGCAAAAT | 83814 |
rs36574720 | snp | C/G | 0.497778 | 0.0332592 | intron-variant | Nedd4l | GRCm38.p3 | 18:64948524 | CACATCTTGGCTGAA[C/G]AGTGACCTACTGGTT | 83814 |
rs36579798 | snp | A/C | 0.142012 | 0.225474 | intron-variant | Nedd4l | Mm_Celera | 18:64995720 | CCTGCGGTACAAGTC[A/C]TCTCAAACATGTGTC | 83814 |
rs36584546 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Nedd4l | Mm_Celera | 18:64982116 | GGCCACCTGTTCCCA[A/G]TAGGACTCTGGTAAG | 83814 |
rs36585066 | snp | A/G | 0.459184 | 0.136902 | intron-variant | Nedd4l | GRCm38.p3 | 18:65004606 | AGGTGGCCAGCAGAG[A/G]TCTTCCACATTTTCA | 83814 |
rs36587525 | snp | A/G | 0.32 | 0.24 | intron-variant | Nedd4l | Mm_Celera | 18:65016415 | ATAGACCAAGGCACC[A/G]GTAGCCAGCCTCCTG | 83814 |
rs36588287 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Nedd4l | Mm_Celera | 18:64977651 | AAGGGCCTGGCTGGT[A/G]TTCTAAAGGCAAGTG | 83814 |
rs36588360 | snp | A/T | 0.142012 | 0.225474 | intron-variant | Nedd4l | Mm_Celera | 18:64981875 | CGTGAAGGACGTGCG[A/T]CGTGTTCATTGTTCC | 83814 |
rs36589582 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Nedd4l | Mm_Celera | 18:64952546 | TGTGTGAAGCCTCAG[C/T]GCCTGTCAGGTATTT | 83814 |
rs36589645 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Nedd4l | Mm_Celera | 18:65028962 | AATCTTCAAGATTAA[A/G]ATGTTCACGCATGTG | 83814 |
rs36591906 | snp | G/T | 0.489796 | 0.070696 | intron-variant | Nedd4l | Mm_Celera | 18:64893796 | TTCGGGAATCTGGGA[G/T]ACTTCTATAGGCTTA | 83814 |
rs36598036 | snp | C/T | 0.495868 | 0.0452663 | intron-variant | Nedd4l | GRCm38.p3 | 18:64962274 | CATTGATGCCAATAC[C/T]TCTAGTGCTGTTGTC | 83814 |
rs36600688 | snp | A/G | 0.497041 | 0.0383476 | intron-variant | Nedd4l | Mm_Celera | 18:64915409 | ATCCATGTGTTTTCA[A/G]TCTCCCTTTCAGAGC | 83814 |
rs36602032 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Nedd4l | Mm_Celera | 18:65001761 | AATGGGATGCCAAGG[C/T]GTAAGATGCAGATTG | 83814 |
rs36606761 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Nedd4l | Mm_Celera | 18:64928651 | TTAAGTCAACCTCTG[A/G]TATGCAAATGCTACC | 83814 |
rs36607415 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Nedd4l | Mm_Celera | 18:64989887 | CAGAGACAGATATTT[C/T]GGTGGACATCACCCG | 83814 |
rs36608742 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Nedd4l | Mm_Celera | 18:64974615 | CAGGAGAATGGTCTG[C/T]AGGTTACCTTACGTA | 83814 |
rs36611237 | snp | A/T | 0.408163 | 0.193609 | intron-variant | Nedd4l | Mm_Celera | 18:65010535 | ATTGAAAGAAAGACT[A/T]CCAAATTTTAGTGGT | 83814 |
rs36611281 | snp | A/G | 0.5 | 0 | intron-variant | Nedd4l | GRCm38.p3 | 18:64933215 | AGCCCTACATCCTCT[A/G]TGTGACAGGGTGTCA | 83814 |
rs36611425 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Nedd4l | Mm_Celera | 18:65042766 | GTAGCACAATCCTGA[C/T]GATAAGAACGGCTAT | 83814 |
rs36617629 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Nedd4l | Mm_Celera | 18:64991202 | ATATTTCCTAGATAC[C/T]TTGCTGCATAGATAT | 83814 |
rs36618708 | snp | A/T | 0.489796 | 0.070696 | intron-variant | Nedd4l | GRCm38.p3 | 18:64949621 | GAAGTCAGCCACATC[A/T]CCACCGAGCATTTGT | 83814 |
rs36620702 | snp | A/G | 0.5 | 0 | intron-variant, upstream-variant-2KB | Nedd4l | GRCm38.p3 | 18:64975533 | GAGTTGGCTGGCCAC[A/G]TTGTTCCTGGCCAAG | 83814 |
rs36621139 | snp | A/G | 0.426035 | 0.177515 | intron-variant | Nedd4l | GRCm38.p3 | 18:65034443 | CCCTGAGGAACACTA[A/G]GTGGCGGCCACCAGA | 83814 |
rs36622499 | snp | C/G | 0.497041 | 0.0383476 | intron-variant | Nedd4l | GRCm38.p3 | 18:64962263 | AGTCTCTGCACCATT[C/G]ATGCCAATACTTCTA | 83814 |
rs36630117 | snp | G/T | 0.426035 | 0.177515 | intron-variant | Nedd4l | GRCm38.p3 | 18:64955415 | AGGAGACATCTCAAG[G/T]TTGTCACTCCTAAAG | 83814 |
rs36631018 | snp | A/T | 0.42 | 0.183303 | intron-variant | Nedd4l | GRCm38.p3 | 18:64927308 | ACTGCCAGTTCCTTG[A/T]AGGCATTTCTATAGT | 83814 |
rs36631648 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Nedd4l | GRCm38.p3 | 18:65007378 | CCACCCATCGTTTAT[C/T]CTGAAACACCCACAT | 83814 |
rs36635382 | snp | C/G | 0.142012 | 0.225474 | intron-variant | Nedd4l | Mm_Celera | 18:64927955 | GATCTTCTGAGCATC[C/G]AAGCCAACTCTTCCT | 83814 |
rs36636760 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Nedd4l | Mm_Celera | 18:65004805 | AGTGTCCAGACTTTT[A/G]ACCTTTTATCTTAGA | 83814 |
rs36637302 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Nedd4l | Mm_Celera | 18:64960098 | ATTTCCCTTTTATAG[C/T]GTTGGGACTCAGGAA | 83814 |
rs36639804 | snp | A/G | 0.493827 | 0.0552116 | intron-variant | Nedd4l | GRCm38.p3 | 18:64961214 | TTTCTTTTTTCTAAA[A/G]GTCAGAACATCTTTC | 83814 |
rs36641744 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Nedd4l | Mm_Celera | 18:64929878 | GTCACTGGACTGTGT[A/G]TCATTCACCGTGGCC | 83814 |
rs36642558 | snp | C/T | 0.165289 | 0.235211 | intron-variant | Nedd4l | Mm_Celera | 18:64955109 | GGAGAGACTCCAGCC[C/T]GGGTTAGACTTCAGT | 83814 |
rs36642732 | snp | G/T | 0.5 | 0 | intron-variant | Nedd4l | Mm_Celera | 18:64956999 | AAGATAACAGGTCTG[G/T]GACATAAACAATGAA | 83814 |
rs36642894 | snp | C/T | 0.493827 | 0.0552116 | intron-variant | Nedd4l | Mm_Celera | 18:64949503 | GGAGCAGAAAAACAT[C/T]GCATCCTCATTTCCA | 83814 |
rs36643093 | snp | A/G | 0.375 | 0.216506 | intron-variant | Nedd4l | Mm_Celera | 18:64978459 | CCCAGGTGACTGAAA[A/G]TAACCCTTGATGCCC | 83814 |
rs36647788 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Nedd4l | Mm_Celera | 18:64954129 | CATGTCGTCTGAAAA[A/G]TGTGTGAACAAAGTT | 83814 |
rs36649264 | snp | A/G | 0.165289 | 0.235211 | intron-variant | Nedd4l | Mm_Celera | 18:64993993 | GATGAAGACTCCTGG[A/G]GTGCAAGTCCTCTCA | 83814 |
rs36652009 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Nedd4l | Mm_Celera | 18:65064778 | TGTAGCATTCACTGC[C/T]GGTTCCTCGATTCCT | 83814 |
rs36652482 | snp | C/T | 0.497041 | 0.0383476 | intron-variant | Nedd4l | GRCm38.p3 | 18:64913636 | TCTATAGGACCCCAG[C/T]CTCAAGGGTTTCGAG | 83814 |
rs36653926 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Nedd4l | Mm_Celera | 18:64911892 | CAAGCCGGTGCTTAC[A/G]ATTGTAGCAATTAGC | 83814 |
rs36654234 | snp | A/G | 0.18 | 0.24 | intron-variant | Nedd4l | Mm_Celera | 18:64962881 | CCCTGGCAGCTCCCG[A/G]CTGCAGCGAGTTTGT | 83814 |
rs36657685 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Nedd4l | Mm_Celera | 18:64988198 | CTGGAAACAAGTTAT[C/T]ACAATTCAGGTCCTC | 83814 |
rs36664797 | snp | A/G | 0.497041 | 0.0383476 | intron-variant | Nedd4l | GRCm38.p3 | 18:64978903 | CCTTCTGAAAAGTAC[A/G]TTTTCTGTTGCAAAG | 83814 |
rs36665090 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Nedd4l | Mm_Celera | 18:64953927 | ATTTTCAAGGCATTT[A/G]GAAATGATGTCAGCC | 83814 |
rs36667931 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Nedd4l | Mm_Celera | 18:65069675 | TGTCCCGGAAGGTTG[A/G]GCAGCAGGGTAAACC | 83814 |
rs36669860 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Nedd4l | Mm_Celera | 18:64900039 | GCGATGTTAGGTCTC[C/T]GGCCAAATTGGTTCT | 83814 |
rs36670176 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Nedd4l | Mm_Celera | 18:64982287 | TCTTCCCTAAACCAC[A/G]ATTAAACATTCATAT | 83814 |
rs36670227 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Nedd4l | Mm_Celera | 18:65070464 | ACCACAAATGCATCC[C/T]TGTGGACGTGGAGCA | 83814 |
rs36670822 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Nedd4l | Mm_Celera | 18:65058432 | AGCCCAGCATGCTTA[A/G]CTTAAAGATGAGTGT | 83814 |
rs36671891 | snp | C/T | 0.495868 | 0.0452663 | intron-variant | Nedd4l | Mm_Celera | 18:64927370 | TACATACCTTAAATT[C/T]TATCAGAAGACTGCT | 83814 |
rs36674836 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Nedd4l | Mm_Celera | 18:64988211 | ATCACAATTCAGGTC[C/T]TCTACTGTCAGGGAG | 83814 |
rs36686327 | snp | A/G/T | 0.48 | 0.0979796 | intron-variant, upstream-variant-2KB | Nedd4l | GRCm38.p3 | 18:65074412 | GATTGGGCAGTAAAC[A/G/T]TATGTTTTCTTGATA | 83814 |
rs36687464 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Nedd4l | Mm_Celera | 18:65026646 | TGCCCTGTCCAGAGG[C/T]ATATGTCCCTTCTTC | 83814 |
rs36688165 | snp | C/T | 0.497041 | 0.0383476 | intron-variant | Nedd4l | GRCm38.p3 | 18:64913090 | ATGGCTAGGTCACTT[C/T]TTGTTTAGTTCATTT | 83814 |
rs36692117 | snp | C/T | 0.493827 | 0.0552116 | intron-variant | Nedd4l | GRCm38.p3 | 18:64951356 | GTATTCCTTTGGACT[C/T]GTTCATGAATTGGCG | 83814 |
rs36693747 | snp | G/T | 0.345679 | 0.230967 | intron-variant | Nedd4l | GRCm38.p3 | 18:64957671 | AAGGGAGTTCATGTC[G/T]GTATAGTTCCCTGTC | 83814 |
rs36696124 | snp | A/C | 0.5 | 0 | intron-variant | Nedd4l | GRCm38.p3 | 18:64952661 | CTCTGGGCCCAGTAA[A/C]AATCCCCTGCTTCCT | 83814 |
rs36706279 | snp | G/T | 0.48 | 0.0979796 | intron-variant, upstream-variant-2KB | Nedd4l | GRCm38.p3 | 18:64976811 | AATTCAAACTTCAGT[G/T]CTTTGACCTTGGCAC | 83814 |
rs36707039 | snp | C/T | 0.459184 | 0.136902 | intron-variant, upstream-variant-2KB | Nedd4l | Mm_Celera | 18:65074944 | TATATCTGAAAATCA[C/T]CCATAGTCCAAAACC | 83814 |
rs36707041 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Nedd4l | Mm_Celera | 18:64951138 | TCATGGAGGCAGCAT[A/G]TCAGAACCATGCAGG | 83814 |
rs36710424 | snp | C/T | 0.426035 | 0.177515 | intron-variant | Nedd4l | GRCm38.p3 | 18:65034818 | ATTTGAGTGTTATTT[C/T]CAGATGCCTCGAGCC | 83814 |
rs36712967 | snp | C/G | 0.426035 | 0.177515 | intron-variant | Nedd4l | GRCm38.p3 | 18:65042002 | ACAGAGTAAAATGAG[C/G]CACTGCTTGAAACCC | 83814 |
rs36716662 | snp | A/G | 0.345679 | 0.230967 | intron-variant | Nedd4l | Mm_Celera | 18:64898316 | ACACTTGATCTTTGT[A/G]TTTCTATTCTATGCA | 83814 |
rs36720064 | snp | C/T | 0.375 | 0.216506 | intron-variant | Nedd4l | GRCm38.p3 | 18:65042604 | GGTTAACCATCACAA[C/T]GTGGTAAGACACCTG | 83814 |
rs36720114 | snp | G/T | 0.497041 | 0.0383476 | intron-variant | Nedd4l | GRCm38.p3 | 18:64946024 | TCAGACATTTCTGCT[G/T]CTGGTGTGGCTGGGA | 83814 |
rs36720338 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Nedd4l | Mm_Celera | 18:65028871 | TAAGGCAACTTCGCC[C/T]GTTAATTAATTCACT | 83814 |
rs36722898 | snp | A/G | 0.497041 | 0.0383476 | intron-variant | Nedd4l | GRCm38.p3 | 18:64951203 | TTCCCAAGGGCCAGA[A/G]CTATAGGGGAAGCCG | 83814 |
rs36725206 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Nedd4l | Mm_Celera | 18:65059363 | ATCTTTTGATCAGAT[C/T]CCTGAGTGATTTCTA | 83814 |
rs36729196 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Nedd4l | Mm_Celera | 18:64987706 | TCTCACATTGAAGAC[A/G]TGACTGAAATTGAGA | 83814 |
rs36730562 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Nedd4l | Mm_Celera | 18:64995148 | AACACTCCAGGTTTA[A/G]CAGGTATCCACTTCT | 83814 |
rs36730806 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Nedd4l | Mm_Celera | 18:64892215 | CACTTAAGGGCAGCT[C/T]GCCTGTAGATAGCAT | 83814 |
rs36745074 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Nedd4l | GRCm38.p3 | 18:64922555 | TTTGTCTGGAGATCC[C/T]ACCGATGACCTCTGC | 83814 |
rs36745615 | snp | C/G/T | 0.132653 | 0.220748 | intron-variant, upstream-variant-2KB | Nedd4l | GRCm38.p3 | 18:64974926 | CAGATGCCCATAGCA[C/G/T]GTTACTACACTGTGA | 83814 |
rs36747144 | snp | C/G | 0.396694 | 0.202437 | intron-variant | Nedd4l | GRCm38.p3 | 18:65042690 | AGCAGCTTTCATCCC[C/G]GTGTCTTTTAGAAGT | 83814 |
rs36749464 | snp | A/G | 0.46281 | 0.131194 | intron-variant | Nedd4l | GRCm38.p3 | 18:64961280 | GGGCTGGAGTGGGGT[A/G]AGCGAGTTTTTGAAT | 83814 |
rs36750336 | snp | C/T | 0.486111 | 0.0821678 | intron-variant, upstream-variant-2KB | Nedd4l | GRCm38.p3 | 18:64975507 | CCTGAGACAGAGCTG[C/T]GGTCTGAGTGGAGTT | 83814 |
rs36755318 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Nedd4l | Mm_Celera | 18:64952534 | CACGATGGACTCTGT[C/G]TGAAGCCTCAGCGCC | 83814 |
rs36758198 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Nedd4l | Mm_Celera | 18:64989916 | CGGTGCCACTTCCAC[A/G]TGGTCTAAGACCATT | 83814 |
rs36766338 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Nedd4l | GRCm38.p3 | 18:64979028 | TTCTGAAAGATGAAG[C/T]TGTGGGCCACGTGGA | 83814 |
rs36766432 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Nedd4l | Mm_Celera | 18:64914302 | AGACAGGGTTCGAGG[C/T]ACCAGCTCTGCAGTG | 83814 |
rs36768494 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Nedd4l | GRCm38.p3 | 18:64954535 | CTATTCGGTCCTCAC[A/G]CCCTGTGTATCTCCT | 83814 |
rs36768825 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Nedd4l | GRCm38.p3 | 18:64957206 | GTGTAACCCTTGCTC[C/T]GTGTGGCACAGTGTG | 83814 |
rs36769196 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Nedd4l | Mm_Celera | 18:64953191 | CATTGTTCCTGAGAT[C/T]TCACCACTTGGTCTG | 83814 |
rs36774391 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Nedd4l | Mm_Celera | 18:65064348 | GTGAAGCCTTCCTCT[C/T]GTCTGAAGTAGATGC | 83814 |
rs36781327 | snp | A/G | 0.497041 | 0.0383476 | intron-variant, upstream-variant-2KB | Nedd4l | GRCm38.p3 | 18:64975366 | TTGTTCTCCCTTGTG[A/G]GTAAGAATGCCTGTG | 83814 |
rs36781883 | snp | A/G | 0.489796 | 0.070696 | intron-variant | Nedd4l | GRCm38.p3 | 18:64950915 | CCCTTGAGGGCTCCC[A/G]TCTCTGGTGTCTTTC | 83814 |
rs36786900 | snp | A/G | 0.459184 | 0.136902 | intron-variant | Nedd4l | GRCm38.p3 | 18:64948597 | TTCTCCTTGGCCTTT[A/G]AGCAAACAAATGTAG | 83814 |
rs36790117 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Nedd4l | Mm_Celera | 18:64984773 | ATCTATGTGACTAAA[A/G]GAACAGAACATCTAT | 83814 |
rs36790947 | snp | A/C | 0.142012 | 0.225474 | intron-variant | Nedd4l | Mm_Celera | 18:64995129 | GTCTGAGTTGAACGT[A/C]AGCAACACTCCAGGT | 83814 |
rs36795083 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Nedd4l | Mm_Celera | 18:64945992 | ATCAGTCTCCTTTTC[C/T]GTGATGGTGCGGGCT | 83814 |
rs36798084 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Nedd4l | Mm_Celera | 18:65026407 | TAAGGTTAAAGATAG[C/T]GTTTAGAGTAACAAA | 83814 |
rs36799123 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Nedd4l | Mm_Celera | 18:65061085 | ACAAGTTGTTCCCCT[C/T]AAACTCCTGACTTTT | 83814 |
rs36802368 | snp | C/T | 0.345679 | 0.230967 | intron-variant | Nedd4l | GRCm38.p3 | 18:64954339 | AAACAGAGTTGAGTG[C/T]GGTTTAAGTAGCTAT | 83814 |
rs36802691 | snp | C/T | 0.375 | 0.216506 | intron-variant | Nedd4l | Mm_Celera | 18:64978904 | CTTCTGAAAAGTACA[C/T]TTTCTGTTGCAAAGA | 83814 |
rs36811290 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Nedd4l | Mm_Celera | 18:65026616 | GAGACATTTACATAA[A/G]GCATGTGCTTCATGT | 83814 |
rs36812698 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Nedd4l | Mm_Celera | 18:65009678 | AGGAGAGTAAGAAAG[C/T]CACTGAAAACCTTGC | 83814 |
rs36813896 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Nedd4l | Mm_Celera | 18:64901851 | GTCGAGTTCTAAATG[C/T]TGATGTAGTTATATA | 83814 |
rs36817554 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Nedd4l | GRCm38.p3 | 18:65056901 | GGGCGTAGTTGTCTT[C/T]GCCTCGCTGTGTCAC | 83814 |
rs36821914 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Nedd4l | Mm_Celera | 18:65060614 | AGCCTCAGATCTAAA[C/T]GGTGGCCTTAGTTTG | 83814 |
rs36822980 | snp | A/G | 0.489796 | 0.070696 | intron-variant | Nedd4l | GRCm38.p3 | 18:64945948 | GGGTGGACGGAAGCC[A/G]TGGCTGTACTGGGGA | 83814 |
rs36830725 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Nedd4l | Mm_Celera | 18:64985029 | TCCGAGCCTGTGCAC[A/G]CCAGGCAGTGTGGGT | 83814 |
rs36835685 | snp | C/T | 0.495868 | 0.0452663 | intron-variant | Nedd4l | GRCm38.p3 | 18:64964321 | AGTAGATCAGCTTCT[C/T]TGTCCTCCCACCACA | 83814 |
rs36836040 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Nedd4l | Mm_Celera | 18:64898640 | taaggatgtgtgcac[C/T]acaggattctgcTCT | 83814 |
rs36836628 | snp | A/G | 0.495868 | 0.0452663 | intron-variant | Nedd4l | GRCm38.p3 | 18:64954670 | CTCCCTTTGGTCCTT[A/G]TGCCATCAACATCCC | 83814 |
rs36841202 | snp | C/G | 0.46281 | 0.131194 | intron-variant | Nedd4l | Mm_Celera | 18:64897511 | GGGTAGGACGTAGCA[C/G]TGAAGAATATTGATT | 83814 |
rs36846121 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Nedd4l | Mm_Celera | 18:65058397 | CTGTTTTAGGTTTCA[A/G]AGTGCCAGTGAATGG | 83814 |
rs36850586 | snp | C/T | 0.426035 | 0.177515 | intron-variant | Nedd4l | Mm_Celera | 18:65035178 | CAGAAGTGGTTTAAT[C/T]TAGGATTTCAGGTAT | 83814 |
rs36851705 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Nedd4l | Mm_Celera | 18:65030572 | CACTCCATGAACACT[A/G]AAGGGACACTGTAGT | 83814 |
rs36855102 | snp | C/T | 0.375 | 0.216506 | intron-variant | Nedd4l | GRCm38.p3 | 18:65042294 | GTTCCTGACAAACAG[C/T]TTGAGTGGTTCATGA | 83814 |
rs36855837 | snp | A/G | 0.297521 | 0.245442 | intron-variant | Nedd4l | Mm_Celera | 18:64942907 | GTTGTAAAATGCGTT[A/G]AATACCAGCAGTACA | 83814 |
rs36859608 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Nedd4l | Mm_Celera | 18:64989584 | ATAATGGGCAAGATA[A/G]TGAAATCCCTGACTT | 83814 |
rs36860890 | snp | A/T | 0.132653 | 0.220748 | intron-variant | Nedd4l | Mm_Celera | 18:64998845 | TATTTTGTGGTGGAA[A/T]GGTCTCAAAAGAGGG | 83814 |
rs36863655 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Nedd4l | GRCm38.p3 | 18:64949484 | ATCCAGACTCCATTG[C/T]TTCGGAGCAGAAAAA | 83814 |
rs36866478 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Nedd4l | Mm_Celera | 18:65070118 | TTTTTTGTAGCTCCT[C/T]GTGTGTCTTAGGTCT | 83814 |
rs36868510 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Nedd4l | Mm_Celera | 18:65026804 | CAGGCCAAGTTCTGC[C/T]TCACACGGGCCAGGT | 83814 |
rs36869964 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Nedd4l | Mm_Celera | 18:64921357 | GTGGTCTCAGAGAAA[A/G]CCTAACTCTCATGCA | 83814 |
rs36872514 | snp | A/C | 0.375 | 0.216506 | intron-variant | Nedd4l | GRCm38.p3 | 18:64913851 | TGAGTTTGGTAACCG[A/C]GGCTGTATGTGCACA | 83814 |
rs36872647 | snp | A/T | 0.486111 | 0.0821678 | intron-variant | Nedd4l | GRCm38.p3 | 18:64926749 | GTGTTTATCAACATG[A/T]ATAGCTACTTTGAGA | 83814 |
rs36873187 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Nedd4l | Mm_Celera | 18:64992085 | GCCCTTGACTTACAT[C/T]CCTTAGCCTCTGAGT | 83814 |
rs36876508 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Nedd4l | Mm_Celera | 18:64984336 | CTTCACAAGGCAAGC[C/T]GACTGAGCTCTGCAG | 83814 |
rs36878134 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Nedd4l | Mm_Celera | 18:64918514 | TTGTTAATCATTGGC[A/G]TTGGCTCAGATGGTA | 83814 |
rs36879294 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Nedd4l | Mm_Celera | 18:64950444 | AACAGTTGGTTAGAC[C/T]CAGCTCTGTTGGTAA | 83814 |
rs36879715 | snp | A/G | 0.345679 | 0.230967 | intron-variant | Nedd4l | Mm_Celera | 18:64904494 | GCCTTGAGAAGCTGT[A/G]AGATGAAGAGGAGAA | 83814 |
rs36883645 | snp | C/T | 0.46281 | 0.131194 | intron-variant | Nedd4l | GRCm38.p3 | 18:65041873 | GCTGAGGAACAAGAC[C/T]GACTCAAAATAAAAC | 83814 |
rs36884966 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Nedd4l | Mm_Celera | 18:64924108 | AGAGATTGTGTAGAA[G/T]GAAGAGGAGTTTCCG | 83814 |
rs36890702 | snp | A/G | 0.495868 | 0.0452663 | intron-variant | Nedd4l | GRCm38.p3 | 18:64961743 | GCTGTAGTTTGCTAT[A/G]AGCTTGTTTGTGCCT | 83814 |
rs36893206 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Nedd4l | Mm_Celera | 18:64927582 | CTTTGTGTATAGACC[C/T]ACTTCTTCAGGCAGG | 83814 |
rs36893440 | snp | A/G | 0.375 | 0.216506 | intron-variant | Nedd4l | Mm_Celera | 18:64937976 | CCACTGTGCCTCCAG[A/G]CTACCTGATGCTGTC | 83814 |
rs36893786 | snp | C/T | 0.46281 | 0.131194 | intron-variant | Nedd4l | Mm_Celera | 18:64957923 | GCAACTGCCTGTGAC[C/T]CTTTAATAAACTCAT | 83814 |
rs36900666 | snp | C/T | 0.124444 | 0.216185 | intron-variant, upstream-variant-2KB | Nedd4l | Mm_Celera | 18:64975296 | GAGCAATTATTTTAG[C/T]GTGCCTTTGCCCATG | 83814 |
rs36902976 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Nedd4l | Mm_Celera | 18:64977733 | GAACACTGAAAATTG[C/T]GAATCGTTTTCCTTA | 83814 |
rs36904701 | snp | C/G | 0.197531 | 0.244432 | intron-variant, upstream-variant-2KB | Nedd4l | GRCm38.p3 | 18:64976418 | AGAAGGATGGCCTCA[C/G]ACTTGGGAGGACATT | 83814 |
rs36905353 | snp | A/G | 0.473373 | 0.11227 | intron-variant | Nedd4l | GRCm38.p3 | 18:64946115 | AGAGGACCTGAAATT[A/G]TTTCCCAGGTCCTAT | 83814 |
rs36905489 | snp | C/T | 0.497041 | 0.0383476 | intron-variant | Nedd4l | GRCm38.p3 | 18:64978988 | ATATACAGAATTCAT[C/T]GTAGCTGGGCCATTC | 83814 |
rs36910515 | snp | C/T | 0.32 | 0.24 | intron-variant | Nedd4l | Mm_Celera | 18:64891948 | TGAGAATGAGCTATA[C/T]GTCATGGCGTTGCAT | 83814 |
rs36910722 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Nedd4l | Mm_Celera | 18:65044675 | TTTTAAGAAAGTGGG[A/G]AAAGATGTGAATGTC | 83814 |
rs36914683 | snp | A/G | 0.473373 | 0.11227 | intron-variant | Nedd4l | GRCm38.p3 | 18:64913919 | CATTCTGGCCACAGA[A/G]GTCCTTTCTCCTCAA | 83814 |
rs36923716 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Nedd4l | Mm_Celera | 18:64953621 | GGTAGTGATTGGTGG[A/G]CAGAGAGCCGATAAC | 83814 |
rs36926145 | snp | A/T | 0.142012 | 0.225474 | intron-variant | Nedd4l | Mm_Celera | 18:64949561 | ACGCAATCAATTAAA[A/T]TTTTCATCGGGTTCA | 83814 |
rs36930675 | snp | C/T | 0.473373 | 0.11227 | intron-variant | Nedd4l | GRCm38.p3 | 18:64996074 | TGTATTGAACACAAT[C/T]CTCTATTTCAGCTTA | 83814 |
rs36935851 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Nedd4l | Mm_Celera | 18:64897811 | AGGCAGAACTGTGGC[A/G]CTTGTGACTACAGTT | 83814 |
rs36937684 | snp | C/G | 0.277778 | 0.248452 | intron-variant | Nedd4l | Mm_Celera | 18:65020190 | TCCTCTTAAACTCAT[C/G]GTTTCATCTTCTTTA | 83814 |
rs36938433 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Nedd4l | GRCm38.p3 | 18:65033110 | TGTTCCCTTTGCTCC[A/G]GATAAGATCAACTGC | 83814 |
rs36939966 | snp | A/G | 0.5 | 0 | intron-variant | Nedd4l | Mm_Celera | 18:64946652 | CTTGTTAGGATTATA[A/G]AATGCAGTATGTGGT | 83814 |
rs36941115 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Nedd4l | Mm_Celera | 18:65021183 | TGCTTTCTTATAAAT[C/T]ACAGCATCGAGTAAG | 83814 |
rs36950176 | snp | G/T | 0.142012 | 0.225474 | intron-variant | Nedd4l | Mm_Celera | 18:64994994 | TCGAGAGGAGGGTGA[G/T]CGGTTTCTCACCAGC | 83814 |
rs36951290 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Nedd4l | Mm_Celera | 18:65045048 | TATGGTTGAGAGTCT[C/T]CCTGTTGCCAGAAAT | 83814 |
rs36957399 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Nedd4l | GRCm38.p3 | 18:65034510 | GCATTTGCTGGGAAA[A/G]GTGTTCAGGAACAAG | 83814 |
rs36961818 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Nedd4l | Mm_Celera | 18:65015728 | CAGCGGAGCCAGCTA[A/G]ATAGAGCCTTGAAAA | 83814 |
rs36962859 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Nedd4l | Mm_Celera | 18:64984316 | ACAGGGGTAGTCATG[C/T]TGACCTTCACAAGGC | 83814 |
rs36969198 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Nedd4l | Mm_Celera | 18:64977348 | CCAGGGATTCTTCCA[C/T]GTCCATTATTGCATG | 83814 |
rs36970828 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Nedd4l | Mm_Celera | 18:64990450 | TTACAACATCTGCTT[A/G]TAAACAGTTAGTGCT | 83814 |
rs36977206 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Nedd4l | Mm_Celera | 18:65068164 | TGTAAGAAAGAGTGT[C/T]GGCACTGCCAGGATT | 83814 |
rs36980886 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Nedd4l | Mm_Celera | 18:65072919 | GGAAGGTCCTCTTGA[A/G]CCTTGTGCATGCAGT | 83814 |
rs36985296 | snp | C/G | 0.42 | 0.183303 | intron-variant | Nedd4l | Mm_Celera | 18:64904542 | TAGTAAGCTTCATTT[C/G]ATTTGCAAGAGGCAA | 83814 |
rs36993267 | snp | A/G | 0.5 | 0 | intron-variant | Nedd4l | GRCm38.p3 | 18:64956639 | CCTCACACCAGACCC[A/G]TTTATTCATCCCAAC | 83814 |
rs36995197 | snp | C/T | 0.426035 | 0.177515 | intron-variant | Nedd4l | GRCm38.p3 | 18:64930492 | GTTATACAACTAGCA[C/T]GGCTTTATGCAGAGG | 83814 |
rs37004126 | snp | C/G | 0.375 | 0.216506 | intron-variant | Nedd4l | Mm_Celera | 18:64949745 | GACCGTTTTTGTGCA[C/G]ATGTTGTGCACATGA | 83814 |
rs37008584 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Nedd4l | Mm_Celera | 18:64924793 | AGTGTGTTAACTACT[C/T]GTTTTTACTCAGCTT | 83814 |
rs37009720 | snp | C/T | 0.497041 | 0.0383476 | intron-variant | Nedd4l | GRCm38.p3 | 18:64926863 | GTGCATCTCTCTGTG[C/T]ATGGCTGGCTCACCC | 83814 |
rs37010294 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Nedd4l | Mm_Celera | 18:65072391 | AAATCACAAGTGGAA[A/G]AATGTGGATGTTCTA | 83814 |
rs37012382 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Nedd4l | Mm_Celera | 18:64914938 | AGGTGACCATTGTTA[A/G]TGAGTTTAAGCAACC | 83814 |
rs37013638 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Nedd4l | GRCm38.p3 | 18:64910960 | CAACACTAAAGCCTT[C/T]TTTTAAAAAGTCATA | 83814 |
rs37013945 | snp | C/T | 0.35503 | 0.226867 | intron-variant | Nedd4l | Mm_Celera | 18:65031618 | CAAATCATCGACCAT[C/T]CAGACAGACAAATGT | 83814 |
rs37018537 | snp | C/T | 0.486111 | 0.0821678 | intron-variant | Nedd4l | GRCm38.p3 | 18:64961709 | GATACTCTTTCCAAG[C/T]GCGGAGCGTTCCCTT | 83814 |
rs37021545 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Nedd4l | Mm_Celera | 18:64999682 | CATGTGGAAGTCAGC[A/G]GACAGCTTCTCTCGT | 83814 |
rs37026045 | snp | G/T | 0.277778 | 0.248452 | intron-variant | Nedd4l | Mm_Celera | 18:65016784 | GGTAGAAGAAATGAT[G/T]CCATGGACCTCGCTG | 83814 |
rs37028434 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Nedd4l | Mm_Celera | 18:64946753 | GTTGGTGGAGAAAGG[A/C]TCCCAAGACATTGTG | 83814 |
rs37028861 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Nedd4l | Mm_Celera | 18:64996771 | ATCTTGTTCCTCAAG[A/G]TGCCATCTACCTTGT | 83814 |
rs37028862 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Nedd4l | Mm_Celera | 18:65058243 | TATCTAGCAGAGAGT[A/G]AAACGTGGTATGCTG | 83814 |
rs37030308 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Nedd4l | Mm_Celera | 18:65042782 | GATAAGAACGGCTAT[C/T]GGTTGAAAATGGCCA | 83814 |
rs37031707 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Nedd4l | Mm_Celera | 18:65042032 | CATCTGACTGGAAAC[C/T]GTAGCAAAGTAGATA | 83814 |
rs37036972 | snp | A/G | 0.165289 | 0.235211 | intron-variant | Nedd4l | Mm_Celera | 18:64958342 | TTAGAAAGAATTCTA[A/G]GAGCAGCAGAAGGAA | 83814 |
rs37043533 | snp | C/G | 0.197531 | 0.244432 | intron-variant | Nedd4l | Mm_Celera | 18:64902980 | AATTAAGTGAGACAC[C/G]CATAGAAGGTCATGG | 83814 |
rs37048360 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Nedd4l | GRCm38.p3 | 18:64978794 | TTCTGTTTTCTTTCT[C/T]GAGTTTATCTCCTTG | 83814 |
rs37052600 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Nedd4l | GRCm38.p3 | 18:64913875 | GTGCACACTCCCATG[A/G]CAGCTACCACCACAC | 83814 |
rs37056376 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Nedd4l | Mm_Celera | 18:65058249 | GCAGAGAGTGAAACG[C/T]GGTATGCTGAGAACA | 83814 |
rs37065935 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Nedd4l | Mm_Celera | 18:64946509 | ACAGGTTGTTCCTGT[C/T]CGGGTACATTTAGAA | 83814 |
rs37068908 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Nedd4l | Mm_Celera | 18:65031995 | TAGAATGTAAATCAG[A/T]TGCAAATATCCAGTG | 83814 |
rs37075080 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Nedd4l | Mm_Celera | 18:64962224 | CAAGACAGTCACCGC[A/G]TGCATTTCCTGAAGA | 83814 |
rs37078648 | snp | A/G | 0.18 | 0.24 | intron-variant | Nedd4l | Mm_Celera | 18:64945316 | GATGAGAGCATTGCA[A/G]AGTGACCTCTCTGGG | 83814 |
rs37079538 | snp | A/T | 0.142012 | 0.225474 | intron-variant | Nedd4l | Mm_Celera | 18:65026779 | ATCATGAGCCATCTC[A/T]GCTCTTTCTCAGGCC | 83814 |
rs37081652 | snp | C/T | 0.336735 | 0.234472 | intron-variant, upstream-variant-2KB | Nedd4l | Mm_Celera | 18:65074298 | CGTTGACTTCTGAAG[C/T]GTTTGCTCATTTGAT | 83814 |
rs37083912 | snp | C/G | 0.46875 | 0.121031 | intron-variant | Nedd4l | Mm_Celera | 18:64941058 | ACAAATGCTTGCTTG[C/G]TGTTAGCCCCAGAAA | 83814 |
rs37088669 | snp | C/G | 0.142012 | 0.225474 | intron-variant | Nedd4l | Mm_Celera | 18:64988678 | TACCTCTCGCCACTC[C/G]CAAGGAAAATATAAC | 83814 |
rs37088718 | snp | A/G | 0.165289 | 0.235211 | intron-variant | Nedd4l | Mm_Celera | 18:64897265 | GGATGCATGAGTTCA[A/G]TGACTCTTTGAGCTG | 83814 |
rs37091805 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Nedd4l | Mm_Celera | 18:64915970 | TGGAACAGATAGCGA[A/T]TGGAAACCAGGATTA | 83814 |
rs37092905 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Nedd4l | Mm_Celera | 18:65029064 | GCCTGTACCCAGAGA[C/T]GCATGTGGTAAATTT | 83814 |
rs37093453 | snp | A/C | 0.396694 | 0.202437 | intron-variant | Nedd4l | Mm_Celera | 18:64905898 | AGATCAGACCCATTA[A/C]ATCCAACAGCACCTT | 83814 |
rs37099424 | snp | A/G | 0.197531 | 0.244432 | intron-variant | Nedd4l | Mm_Celera | 18:64946640 | CTGTATATTTTTCTT[A/G]TTAGGATTATAGAAT | 83814 |
rs37099793 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | Nedd4l | Mm_Celera | 18:64978501 | GGACTTTGAACTTTG[A/G]CTCTAATGGGGGAGT | 83814 |
rs37100343 | snp | C/T | 0.32 | 0.24 | intron-variant | Nedd4l | GRCm38.p3 | 18:64958337 | GGCACTTAGAAAGAA[C/T]TCTAGGAGCAGCAGA | 83814 |
rs37100632 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Nedd4l | Mm_Celera | 18:65007364 | CTCAGCTATAAATAC[C/T]ACCCATCGTTTATCC | 83814 |
rs37104764 | snp | C/T | 0.459184 | 0.136902 | intron-variant | Nedd4l | GRCm38.p3 | 18:65009295 | GGAGTAACAAAGGCA[C/T]CCACATTTTCTTTGA | 83814 |
rs37112725 | snp | C/T | 0.486111 | 0.0821678 | intron-variant | Nedd4l | GRCm38.p3 | 18:64958404 | CACCGAGTGAGCAGT[C/T]GCTAGGGCCTGTTCA | 83814 |
rs37114193 | snp | C/T | 0.497041 | 0.0383476 | intron-variant | Nedd4l | Mm_Celera | 18:64961548 | CATCGGGTTGGGATC[C/T]TTAACTTGTTTACTG | 83814 |
rs37117993 | snp | C/T | 0.495868 | 0.0452663 | intron-variant | Nedd4l | Mm_Celera | 18:64978117 | GATAAATAGTACCCT[C/T]TGGGTTGAAACTTTG | 83814 |
rs37122248 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Nedd4l | Mm_Celera | 18:65059617 | TTCTTACATGGCCTT[A/G]GGATGCTCACTCAAA | 83814 |
rs37123522 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Nedd4l | GRCm38.p3 | 18:64931351 | ATGGTGTACCCATGA[A/G]CCTCAGTGCCTGGGG | 83814 |
rs37125312 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Nedd4l | Mm_Celera | 18:64993726 | TATAGCCTATTACAC[C/T]ATTATATAGCTCGTT | 83814 |
rs37142119 | snp | G/T | 0.142012 | 0.225474 | intron-variant | Nedd4l | Mm_Celera | 18:64963252 | CCGTACTCTGGCAGG[G/T]CCTAGGGATTCCAAG | 83814 |
rs37142245 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Nedd4l | GRCm38.p3 | 18:65008028 | AGCTGAAGTGAATGG[C/T]TCAGACTTGATCATG | 83814 |
rs37142778 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Nedd4l | GRCm38.p3 | 18:64950862 | GGTCTCAGTGTTCCC[G/T]CCATAGCTTCTGTGG | 83814 |
rs37148297 | snp | A/G | 0.21875 | 0.248039 | intron-variant | Nedd4l | Mm_Celera | 18:65034641 | ATTATTAGTGTGTTA[A/G]TTGTTGTCATGAGTC | 83814 |
rs37150949 | snp | A/T | 0.142012 | 0.225474 | intron-variant | Nedd4l | Mm_Celera | 18:64970839 | ATTGCCCTTAAGTAG[A/T]AAATTTGAAGGCAAA | 83814 |
rs37151257 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Nedd4l | Mm_Celera | 18:64968411 | GGCTTTGAATCAGCA[C/T]GGACATTTCTCTACG | 83814 |
rs37158629 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Nedd4l | Mm_Celera | 18:64996273 | AGTGCCAGTGCCTAG[A/G]AGAGACTTAAATACT | 83814 |
rs37160788 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Nedd4l | Mm_Celera | 18:64926602 | TGGAGGTCCTTTGCT[C/T]TCTGTTCTAGGAATT | 83814 |
rs37176592 | snp | A/G | 0.495868 | 0.0452663 | intron-variant | Nedd4l | GRCm38.p3 | 18:64945704 | GCAGAAACTTGCTAA[A/G]GAGCGACTGTCATTA | 83814 |
rs37178379 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Nedd4l | GRCm38.p3 | 18:65034966 | GGGATGCATAGACCT[C/T]GGTCCCTTCAACATC | 83814 |
rs37180289 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Nedd4l | Mm_Celera | 18:64923052 | AGGGCACATACTTAT[C/T]GAATGAGACCCTGTT | 83814 |
rs37182046 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Nedd4l | Mm_Celera | 18:65057621 | ATTCTCAGTACAGCC[A/G]CTGATTTGTTCACTG | 83814 |
rs37189908 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Nedd4l | Mm_Celera | 18:64978248 | ACAGAGTAGTTGTCC[A/G]AGAGGGCTGTGGTGA | 83814 |
rs37200945 | snp | A/T | 0.408163 | 0.193609 | intron-variant | Nedd4l | GRCm38.p3 | 18:64960809 | ATGCAGGTGTCAAAT[A/T]CAAAGAAGTGGGTTC | 83814 |
rs37203156 | snp | C/T | 0.5 | 0 | intron-variant | Nedd4l | GRCm38.p3 | 18:64950515 | AGGATTCACTCAATC[C/T]TTGGTGTACTAAGCC | 83814 |
rs37204122 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Nedd4l | Mm_Celera | 18:65044352 | GTAGAGCCTTGGAAC[A/G]TTAACGATTATAGCA | 83814 |
rs37204602 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Nedd4l | Mm_Celera | 18:64922034 | CCATGGAAATTGTAC[A/G]TGAAAAATGTAGAGG | 83814 |
rs37206685 | snp | A/C | 0.5 | 0 | intron-variant | Nedd4l | GRCm38.p3 | 18:64926918 | CCTGGCTTGCTCTTC[A/C]TTATTATGCACACAG | 83814 |
rs37211362 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Nedd4l | Mm_Celera | 18:64996585 | GATCACTGGCAGATA[C/T]TATCTCAGTCTCCCC | 83814 |
rs37212732 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Nedd4l | Mm_Celera | 18:65060894 | TGGAGAATGTTACGC[C/T]GACATCATCAGAGAG | 83814 |
rs37218944 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Nedd4l | Mm_Celera | 18:64916868 | ATATGTGCTGTTAAT[A/G]GCATATGTAGATCTA | 83814 |
rs37228683 | snp | A/T | 0.277778 | 0.248452 | intron-variant | Nedd4l | GRCm38.p3 | 18:64942466 | GTCTCAGCCTCCCAC[A/T]TGTGACCACCGTTGA | 83814 |
rs37229750 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Nedd4l | Mm_Celera | 18:64994883 | AACCCAGGTGTGAAC[C/T]AGCCTTATCCCGCCT | 83814 |
rs37231011 | snp | C/T | 0.5 | 0 | intron-variant | Nedd4l | GRCm38.p3 | 18:64930107 | TTTTCACACATATTT[C/T]CCAAGCCATAGTGTG | 83814 |
rs37232001 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Nedd4l | Mm_Celera | 18:65018730 | ATGCCTCAAGGTTCA[A/G]TTCATCCCAGATGCA | 83814 |
rs37234312 | snp | C/T | 0.18 | 0.24 | intron-variant | Nedd4l | Mm_Celera | 18:64942421 | GACCTCTAGTATAGC[C/T]CAGGCTGGCCACAAA | 83814 |
rs37237851 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Nedd4l | Mm_Celera | 18:65032634 | CAAGCCTGCATAAAA[C/T]ACTGGCGATGAGTCC | 83814 |
rs37238243 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Nedd4l | GRCm38.p3 | 18:64954892 | CCTCTTTGTTCTGGT[A/T]ACATCTAAAATGTAG | 83814 |
rs37243964 | snp | C/G | 0.244898 | 0.249948 | intron-variant | Nedd4l | Mm_Celera | 18:64909455 | CAACCAATGACCCAG[C/G]CAAAAAGCAACAACA | 83814 |
rs37247750 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Nedd4l | Mm_Celera | 18:64914818 | TTGCTGGCTCCTGCA[A/G]CTGGAGTGGACTTGG | 83814 |
rs37249185 | snp | A/T | 0.18 | 0.24 | intron-variant | Nedd4l | Mm_Celera | 18:64959799 | GGGACTCAGGACACC[A/T]CAGGCGAACACCTGG | 83814 |
rs37252842 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Nedd4l | Mm_Celera | 18:64980502 | CCTGTCTTACAATTT[A/G]AATAAAAGCTAAGTA | 83814 |
rs37255796 | snp | A/G | 0.124444 | 0.216185 | intron-variant, missense, upstream-variant-2KB | Nedd4l | Mm_Celera | 18:65025892 | TAGGGTAAATGACTC[A/G]AACCTGGTTGGGACT | 83814 |
rs37259999 | snp | A/T | 0.336735 | 0.234472 | intron-variant | Nedd4l | Mm_Celera | 18:65070054 | TTCCTTGGCACCTGG[A/T]GGCTCTGTTTACCAC | 83814 |
rs37262758 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Nedd4l | Mm_Celera | 18:64919697 | GGCACCAACCAAGCA[C/T]TCACTAGACCACATC | 83814 |
rs37268849 | snp | A/G | 0.486111 | 0.0821678 | intron-variant | Nedd4l | GRCm38.p3 | 18:64959421 | GTAGGGTACGATTAC[A/G]TGGCTCCAGCACGCT | 83814 |
rs37274316 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Nedd4l | Mm_Celera | 18:64947896 | AGGATATTAAAGCAC[G/T]AAGAGGTGTGCCCGG | 83814 |
rs37274586 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Nedd4l | Mm_Celera | 18:64912044 | TATGGTAATCAAATT[C/T]CTGGCACTGTGTTTT | 83814 |