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 |