SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs3693351 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Ube4a | Mm_Celera | 9:44955803 | TGCCAAGACTCCAAA[C/T]AATCTTCACAGACTA | 140630 |
rs3700385 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ube4a | Mm_Celera | 9:44959809 | CAACTAACATCAAAC[C/T]AACTTTTGCTTTCAC | 140630 |
rs3707713 | snp | C/T | 0.290657 | 0.246672 | intron-variant | Ube4a | Mm_Celera | 9:44955963 | AAATCCTAGAGTGTC[C/T]GTCACTCCTAACGCT | 140630 |
rs6154925 | snp | C/T | 0.5 | 0 | intron-variant | Ube4a | Mm_Celera | 9:44927927 | aacaaaaCAAGATCA[C/T]GATATCCTCAAAGAC | 140630 |
rs6179001 | snp | A/T | 0.207612 | 0.24638 | utr-variant-3-prime | Ube4a | Mm_Celera | 9:44923407 | GCGTTTAGAGTGTGG[A/T]ACTGAGCAGCAACTG | 140630 |
rs6401292 | snp | A/T | 0.48 | 0.0979796 | intron-variant | Ube4a | Mm_Celera | 9:44927512 | GAGTATTAGAGCATA[A/T]TGCCCAAGTAAGTAT | 140630 |
rs6401942 | snp | G/T | 0.5 | 0 | intron-variant | Ube4a | Mm_Celera | 9:44927679 | ttttttcccctgcag[G/T]aagccttggagatga | 140630 |
rs6403063 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Ube4a | Mm_Celera | 9:44927869 | AGTCTTCCTCAGCTA[C/T]AGAGTAAGCTTAAGC | 140630 |
rs13463989 | snp | C/T | 0.124444 | 0.216185 | utr-variant-3-prime | Ube4a | Mm_Celera | 9:44924939 | AATGTCATTTTAGGA[C/T]ACTTAAAACAGTATA | 140630 |
rs29586362 | snp | A/G | 0.492188 | 0.0620098 | missense | Ube4a | Mm_Celera | 9:44944880 | TAGCTCTGGGGGAAC[A/G]TTGGCTCCTGCACAG | 140630 |
rs29591892 | snp | C/T | 0.375 | 0.216506 | intron-variant | Ube4a | Mm_Celera | 9:44929034 | AGGGGGCTGCAAGCA[C/T]GAAACTCCTGTTAGC | 140630 |
rs29592050 | snp | C/T | 0.5 | 0 | intron-variant | Ube4a | Mm_Celera | 9:44952399 | GGAAAAAATTCCAGA[C/T]ACCAGCATTAAGTTT | 140630 |
rs29593162 | snp | A/G | 0.498615 | 0.0262793 | intron-variant | Ube4a | Mm_Celera | 9:44951956 | ACAGGATTCAGCATG[A/G]CTGTTCTGCTGAGGG | 140630 |
rs29593298 | snp | A/G | 0.498615 | 0.0262793 | utr-variant-3-prime | Ube4a | Mm_Celera | 9:44923578 | GGTGAGGTGTGAGCC[A/G]ACTGAAGTCTTCACT | 140630 |
rs29594357 | snp | C/T | 0.5 | 0 | intron-variant | Ube4a | Mm_Celera | 9:44926334 | ACTCAAGAGATCCAC[C/T]TGCTTCTGCCTCCCA | 140630 |
rs29594418 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ube4a | Mm_Celera | 9:44964066 | CACATATGGCATGCA[C/T]ATATACAGAAACACA | 140630 |
rs29596160 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Ube4a | Mm_Celera | 9:44939287 | CATGGAGGCTGAAAG[C/T]CTACACCAAGTGCCT | 140630 |
rs29598316 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ube4a | Mm_Celera | 9:44928108 | TGGCTCACAACCATC[C/T]GTAACAAAATCTGAT | 140630 |
rs29601381 | snp | A/C | 0.475309 | 0.108333 | intron-variant | Ube4a | Mm_Celera | 9:44944685 | GACTCAGGTAAATTT[A/C]AACCAGTGCATGTGA | 140630 |
rs29635360 | snp | C/T | 0.465374 | 0.126941 | intron-variant | Ube4a | Mm_Celera | 9:44934900 | GGTTTTGTATATGCT[C/T]TGTATGTGCTCTATC | 140630 |
rs29637352 | snp | A/G | 0.5 | 0 | intron-variant | Ube4a | Mm_Celera | 9:44933988 | TGTGCACCTACATGT[A/G]TTACAGCAAGTGTAT | 140630 |
rs29638978 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ube4a | Mm_Celera | 9:44926570 | AATGTCTTTTTCTGA[C/T]CTCTGTGAGCACTAG | 140630 |
rs29642225 | snp | A/C | 0.5 | 0 | upstream-variant-2KB | Ube4a | Mm_Celera | 9:44967370 | GCCTTTAATTCCAGC[A/C]CTTGGAGACAGGGCA | 140630 |
rs29683134 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ube4a | Mm_Celera | 9:44946813 | AGGTGATAAATCCTT[C/T]GGCTCAATTTTTCAA | 140630 |
rs29686320 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ube4a | Mm_Celera | 9:44928789 | GTTTGAGGCCAGCCT[A/G]TGTAACAGCATGATC | 140630 |
rs29687203 | snp | C/T | 0.455 | 0.143091 | intron-variant | Ube4a | Mm_Celera | 9:44954658 | ACTGAACTGTATTTC[C/T]GGCCCTATTTTTTGT | 140630 |
rs29690751 | snp | G/T | 0.444444 | 0.157135 | upstream-variant-2KB | Ube4a | Mm_Celera | 9:44965771 | CGGGGCAGGGTTGGC[G/T]ATGACTGCGTGCTTT | 140630 |
rs29693119 | snp | A/G | 0.5 | 0 | intron-variant | Ube4a | Mm_Celera | 9:44935836 | AGAGCACTTGTTCTC[A/G]CATATGGCAGCTCAC | 140630 |
rs29693805 | snp | A/G | 0.475309 | 0.108333 | intron-variant | Ube4a | Mm_Celera | 9:44947157 | GTTAGTTTGGCCACT[A/G]TTGTAGTCTGCTAAA | 140630 |
rs29697035 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Ube4a | Mm_Celera | 9:44927171 | ACACATAAATAACTG[A/T]ATGTAATTTAAAAAT | 140630 |
rs29734602 | snp | A/T | 0.375 | 0.216506 | intron-variant | Ube4a | Mm_Celera | 9:44952252 | TGGAGACTAAAGGCA[A/T]ATACTGCTGTGCTCA | 140630 |
rs29737367 | snp | A/G | 0.5 | 0 | intron-variant | Ube4a | Mm_Celera | 9:44946009 | CAGAATCAGACGGAA[A/G]GTCTCAACAAGGCCT | 140630 |
rs29740094 | snp | C/T | 0.487535 | 0.077957 | intron-variant | Ube4a | Mm_Celera | 9:44950998 | AAGATATAAGAAGTC[C/T]GATACATGCCTTGGC | 140630 |
rs29782200 | snp | A/G | 0.375 | 0.216506 | intron-variant | Ube4a | Mm_Celera | 9:44948675 | GGATTCTAGGCGTGT[A/G]ATACCACACTTGGCT | 140630 |
rs29782564 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ube4a | Mm_Celera | 9:44928515 | CCAGCACTTGGGAGG[C/T]AGAGGTAGGCAGATT | 140630 |
rs29782729 | snp | A/T | 0.32 | 0.24 | intron-variant | Ube4a | GRCm38.p3 | 9:44950524 | TTGTTGTGGTTGATT[A/T]TTTTTTTTTTTTTTC | 140630 |
rs29783407 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Ube4a | Mm_Celera | 9:44954406 | TTTCTGAGTTCGAGG[C/T]CAGCCTGGTCTACAG | 140630 |
rs29785479 | snp | C/T | 0.375 | 0.216506 | intron-variant | Ube4a | Mm_Celera | 9:44945250 | GTCTCTGTGTAGCTC[C/T]GGTTTTCAAGGAACT | 140630 |
rs29788003 | snp | G/T | 0.498615 | 0.0262793 | intron-variant | Ube4a | Mm_Celera | 9:44936400 | AGGATGACAGGAAAA[G/T]GAATCCTTCCTAAAA | 140630 |
rs29794258 | snp | A/G | 0.484429 | 0.0868505 | intron-variant | Ube4a | Mm_Celera | 9:44964978 | CTATGGTCAATCTGA[A/G]AAATGTTTTCTCGAC | 140630 |
rs29832049 | snp | C/G | 0.197531 | 0.244432 | intron-variant | Ube4a | Mm_Celera | 9:44965461 | AGCCTCAACACTCTC[C/G]TCCTCTTATACCTTG | 140630 |
rs29834724 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Ube4a | Mm_Celera | 9:44926464 | AATGGCTCAGTCATA[A/T]GTGCATTGAATGCTC | 140630 |
rs29836238 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Ube4a | Mm_Celera | 9:44939299 | AAGCCTACACCAAGT[A/G]CCTTCTTCAAATGCT | 140630 |
rs29836850 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ube4a | Mm_Celera | 9:44928289 | AAATAGGCACCATGT[C/T]TCTCAGCACCCTTCT | 140630 |
rs29839137 | snp | G/T | 0.5 | 0 | intron-variant | Ube4a | Mm_Celera | 9:44928736 | ACTGTAGGCCTAAGT[G/T]TTTTAGGAATGTGAA | 140630 |
rs29839211 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ube4a | Mm_Celera | 9:44948441 | TGTGTGTGTGTGTGT[A/G]TGTGTATACGTACAC | 140630 |
rs29843535 | snp | A/G | 0.5 | 0 | intron-variant | Ube4a | Mm_Celera | 9:44936333 | GCTAGGATGCGATCC[A/G]GATGGAAAGGAGCAT | 140630 |
rs29845378 | snp | A/C | 0.5 | 0 | upstream-variant-2KB | Ube4a | Mm_Celera | 9:44967083 | AGCCCTAACACCCAT[A/C]TACACAAAATAAAAA | 140630 |
rs29878658 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ube4a | Mm_Celera | 9:44948747 | CAACTTATTAAAATG[C/T]CAGCACCAAGAGAAT | 140630 |
rs29880837 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ube4a | Mm_Celera | 9:44937406 | TAACGCTCTGGGAGG[C/T]TAAGGTGAAAGGATC | 140630 |
rs29883173 | snp | A/G | 0.5 | 0 | intron-variant | Ube4a | Mm_Celera | 9:44926035 | TAAGACCCTAGGGCC[A/G]AGCAGAGCATCTGAA | 140630 |
rs29891143 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Ube4a | Mm_Celera | 9:44927423 | AGTGCAGTGGAACTG[A/C]GTTTGTTCATGAATT | 140630 |
rs29893716 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Ube4a | Mm_Celera | 9:44958991 | AAACCATCTGTAATG[G/T]GATCCAATGCCCTCT | 140630 |
rs29895389 | snp | G/T | 0.5 | 0 | intron-variant | Ube4a | Mm_Celera | 9:44946651 | CCCTTTTCCCCTTTT[G/T]TACCTGATTTTCTGA | 140630 |
rs29929720 | snp | A/G | 0.465374 | 0.126941 | intron-variant | Ube4a | Mm_Celera | 9:44950154 | CACTTGGCAGTATTG[A/G]TTTCTTGGGGACTGA | 140630 |
rs29937731 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Ube4a | Mm_Celera | 9:44957253 | TCTGTTTGAAATGTT[A/G]CACTGGGTGATGCCT | 140630 |
rs29940307 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ube4a | Mm_Celera | 9:44928137 | ATGCCCTCTTCTGGA[A/G]TGTCTGAATGTACTT | 140630 |
rs29942928 | snp | A/C | 0.432133 | 0.171253 | synonymous-codon | Ube4a | Mm_Celera | 9:44937876 | CCGATAGCAATCTGT[A/C]CCCCACATGTATCTT | 140630 |
rs29974739 | snp | A/C | 0.493827 | 0.0552116 | intron-variant | Ube4a | Mm_Celera | 9:44931138 | CTACTCATCATTGCT[A/C]AGTTTTTACTGATTT | 140630 |
rs29975169 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Ube4a | Mm_Celera | 9:44951309 | ATTTTTAATTAAACA[C/T]CCAGTCTGATTATTG | 140630 |
rs29979626 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Ube4a | Mm_Celera | 9:44943044 | TACCAGCTGGCCAGA[C/T]GCAAGGTGCACTGTT | 140630 |
rs29983996 | snp | A/G | 0.498615 | 0.0262793 | intron-variant | Ube4a | Mm_Celera | 9:44945564 | CGTTTTCTCCAGTCC[A/G]GTGCCAGCTTTCTTC | 140630 |
rs29986081 | snp | A/T | 0.492188 | 0.0620098 | intron-variant | Ube4a | Mm_Celera | 9:44938008 | TAGAGAACAAGCTTA[A/T]GTGTGTGCATTTTTT | 140630 |
rs29987635 | snp | A/G | 0.432133 | 0.171253 | intron-variant | Ube4a | Mm_Celera | 9:44950489 | ACATCAGCTGACCTG[A/G]TGTTTGGTTTTCTTT | 140630 |
rs30022243 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Ube4a | Mm_Celera | 9:44964045 | TTACTTTTGTGGGCA[G/T]CTGCACACATATGGC | 140630 |
rs30030445 | snp | C/T | 0.375 | 0.216506 | intron-variant | Ube4a | Mm_Celera | 9:44938438 | TGTTGGGATTAGAGT[C/T]GAGTGCCACCACACC | 140630 |
rs30034829 | snp | C/G | 0.375 | 0.216506 | intron-variant | Ube4a | Mm_Celera | 9:44963843 | AGAGAGGGGAAGAAA[C/G]AAAGAGATTAAGAGA | 140630 |
rs30035477 | snp | C/T | 0.5 | 0 | intron-variant | Ube4a | Mm_Celera | 9:44963514 | ACCTATTTTAAGTTT[C/T]CCAGCTTGAGTAGAG | 140630 |
rs30036209 | snp | C/T | 0.49827 | 0.0293608 | intron-variant | Ube4a | Mm_Celera | 9:44941139 | AGTGACTGGGGCAAG[C/T]GTCCCACACATCACC | 140630 |
rs30036300 | snp | A/G/T | 0.375 | 0.216506 | intron-variant | Ube4a | GRCm38.p3 | 9:44963826 | AGGAAAGAAAGAAAG[A/G/T]GAGAGAGGGGAAGAA | 140630 |
rs30037506 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ube4a | Mm_Celera | 9:44959024 | TGGCATGCAGGTGTA[C/T]ATGTAGAGTACATAC | 140630 |
rs30037640 | snp | A/T | 0.498615 | 0.0262793 | intron-variant | Ube4a | Mm_Celera | 9:44945419 | TATTTTTGTGCAGAT[A/T]TTGGTTTTGTTAATT | 140630 |
rs30039695 | snp | C/G | 0.475309 | 0.108333 | intron-variant | Ube4a | Mm_Celera | 9:44962509 | CCTCCAAACCACAAC[C/G]CTTAAGCAAATGTTC | 140630 |
rs30039984 | snp | C/G | 0.32 | 0.24 | intron-variant | Ube4a | Mm_Celera | 9:44952773 | ATGGTTGTGAGCCAT[C/G]ATGTGGTTGCTGGGA | 140630 |
rs30041421 | snp | C/T | 0.455 | 0.143091 | intron-variant | Ube4a | Mm_Celera | 9:44936271 | GAATAATAGTGTCCT[C/T]CTTCAGCTTTGTCTT | 140630 |
rs30044620 | snp | A/C | 0.5 | 0 | intron-variant | Ube4a | Mm_Celera | 9:44933855 | CCTGGACAGCCAGGG[A/C]TACACAGAGAAACCC | 140630 |
rs30045339 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ube4a | Mm_Celera | 9:44944945 | AAGAAGCAAAAGGAA[C/T]GGTGATGGACTGCTC | 140630 |
rs30045718 | snp | A/G | 0.498615 | 0.0262793 | intron-variant | Ube4a | Mm_Celera | 9:44947452 | ATCATCCCCTTTTTA[A/G]TGAAGGACTGAAGAC | 140630 |
rs30072307 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ube4a | Mm_Celera | 9:44928943 | TTGCAGGGGATTCCA[C/T]ATCTTCTTCAGACAT | 140630 |
rs30080066 | snp | A/G | 0.375 | 0.216506 | intron-variant | Ube4a | Mm_Celera | 9:44934203 | TGTTCCACTTCAATG[A/G]GAGTGTTCCTTGAGT | 140630 |
rs30080285 | snp | A/G | 0.444444 | 0.157135 | upstream-variant-2KB | Ube4a | Mm_Celera | 9:44965730 | CCGGAAGTGGCTTTG[A/G]GATTGGGCTAGGCAG | 140630 |
rs30083086 | snp | C/T | 0.375 | 0.216506 | intron-variant | Ube4a | Mm_Celera | 9:44927055 | GTTTGATCTCCAGGA[C/T]CCACAAAGTTGGAGA | 140630 |
rs30084787 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ube4a | Mm_Celera | 9:44961802 | TGCTAGGGATCCCAT[A/G]CTGTTACTTTCCTTA | 140630 |
rs30085561 | snp | A/C | 0.432133 | 0.171253 | intron-variant | Ube4a | Mm_Celera | 9:44952269 | TACTGCTGTGCTCAG[A/C]TTTCAACAACTGTTC | 140630 |
rs30092588 | snp | A/C | 0.375 | 0.216506 | intron-variant | Ube4a | Mm_Celera | 9:44943858 | CCTGTCTTGAACGAA[A/C]GAACAAACAAACAAA | 140630 |
rs30120912 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Ube4a | Mm_Celera | 9:44937394 | TGTCTGCAACCCTAA[A/C]GCTCTGGGAGGCTAA | 140630 |
rs30125578 | snp | C/G/T | 0.387812 | 0.208586 | intron-variant | Ube4a | GRCm38.p3 | 9:44932010 | TTAGTAAGACGGCGG[C/G/T]TCTAGTCATTGACTG | 140630 |
rs30136399 | snp | C/T | 0.5 | 0 | intron-variant | Ube4a | Mm_Celera | 9:44933514 | TAAAGCTCAATGCAG[C/T]TCTAATTTTCTCCTT | 140630 |
rs30137094 | snp | A/T | 0.188366 | 0.242283 | intron-variant | Ube4a | Mm_Celera | 9:44960383 | TGTTTCCATTGCCTA[A/T]ACCTTGACTAGTGCA | 140630 |
rs30173771 | snp | A/G | 0.32 | 0.24 | intron-variant | Ube4a | Mm_Celera | 9:44951492 | CACTATTTCCCATCC[A/G]GGCTGGATGATCAGC | 140630 |
rs30176645 | snp | C/T | 0.375 | 0.216506 | intron-variant | Ube4a | Mm_Celera | 9:44962148 | ATTACAGGCATGTAT[C/T]GCAATGCCTGGCTTG | 140630 |
rs30177507 | snp | C/T | 0.484429 | 0.0868505 | intron-variant | Ube4a | Mm_Celera | 9:44965248 | AAAAGACAGCCACAG[C/T]CCACACTCGGGCCTT | 140630 |
rs30181814 | snp | C/T | 0.5 | 0 | intron-variant | Ube4a | Mm_Celera | 9:44935839 | GCACTTGTTCTCACA[C/T]ATGGCAGCTCACAAA | 140630 |
rs30183187 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Ube4a | Mm_Celera | 9:44954402 | TGGATTTCTGAGTTC[A/G]AGGTCAGCCTGGTCT | 140630 |
rs30184635 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ube4a | Mm_Celera | 9:44932275 | AAAGGCGTGTGCCAC[C/T]ACTGCTCCGCGTCTC | 140630 |
rs30185595 | snp | C/T | 0.455 | 0.143091 | intron-variant | Ube4a | Mm_Celera | 9:44951086 | ACTAATTATATCCAT[C/T]GTTACTGTAATTAAG | 140630 |
rs30192786 | snp | G/T | 0.375 | 0.216506 | intron-variant | Ube4a | Mm_Celera | 9:44931956 | TCTTTTCACCTGGTA[G/T]AAACATCTTCGATTA | 140630 |
rs30217130 | snp | A/G | 0.5 | 0 | intron-variant | Ube4a | Mm_Celera | 9:44954333 | AACAGGGGCTCCTAA[A/G]CCGGGCGAGGTGGCT | 140630 |
rs30224521 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Ube4a | Mm_Celera | 9:44963666 | ATGACTCTACCAGAG[G/T]ACCAGAGTCTGGATC | 140630 |
rs30225550 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ube4a | Mm_Celera | 9:44949007 | TAGACAGACGAGAAA[A/G]GAAGGAGGCTGTGAC | 140630 |