SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs26913986 | snp | C/T | 0.5 | 0 | upstream-variant-2KB, intron-variant | Rnf185, 8430429K09Rik | Mm_Celera | 11:3454837 | TGCCAGCAGTTCCAG[C/T]TGCTAGGACCTATAT | 193670 |
rs26913987 | snp | G/T | 0.32 | 0.24 | upstream-variant-2KB, intron-variant | Rnf185, 8430429K09Rik | Mm_Celera | 11:3454763 | ATTCTAATCACCGAG[G/T]GACCAAAGGCAGTTA | 193670 |
rs26913988 | snp | C/G | 0.152778 | 0.230321 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | Rnf185, 8430429K09Rik | Mm_Celera | 11:3452434 | CCCAGGCGCCCGGCT[C/G]GTAAGTTCCGCCCCG | 193670 |
rs26913989 | snp | A/G | 0.152778 | 0.230321 | intron-variant, upstream-variant-2KB | Rnf185, 8430429K09Rik | Mm_Celera | 11:3451584 | GCTGCCTCGAATCGA[A/G]TACCGCATTCACAGC | 193670 |
rs26913990 | snp | A/G | 0.32 | 0.24 | intron-variant | Rnf185 | Mm_Celera | 11:3449917 | TTTCACAGGCCAGCA[A/G]AACACATTTACATCA | 193670 |
rs26913991 | snp | A/T | 0.46875 | 0.121031 | intron-variant | Rnf185 | Mm_Celera | 11:3447279 | TCTCCACATGCACAC[A/T]TGGCATGCACACTTT | 193670 |
rs26913992 | snp | G/T | 0.152778 | 0.230321 | intron-variant | Rnf185 | Mm_Celera | 11:3445069 | CAATGCATCTTGGAC[G/T]GTTTTCATATTGCAA | 193670 |
rs26913993 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Rnf185 | Mm_Celera | 11:3443014 | TTTCTACCTAAAGTG[C/T]TGAAGTCAAGGGCAT | 193670 |
rs26913994 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Rnf185 | Mm_Celera | 11:3442949 | GCCTGGGTAACTATG[A/C]ACTGGTAGGAAATGT | 193670 |
rs26913995 | snp | G/T | 0.260355 | 0.249785 | intron-variant | Rnf185 | Mm_Celera | 11:3440015 | AACTACAGTCAAAAT[G/T]CCTAAGCTTCTAAAA | 193670 |
rs26913996 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Rnf185 | Mm_Celera | 11:3438470 | GATTTTAATGATTCT[C/T]TCCCCATCTAGTTCC | 193670 |
rs26913997 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Rnf185 | Mm_Celera | 11:3438345 | AATGGTGAGGAACCA[A/G]GAAGAGCAGGGAAAA | 193670 |
rs26913998 | snp | C/T | 0.32 | 0.24 | intron-variant, utr-variant-5-prime | Rnf185 | Mm_Celera | 11:3438312 | TGAGCCAAAAGTCAG[C/T]GTAGGAGGAGCCTAG | 193670 |
rs26913999 | snp | C/T | 0.297521 | 0.245442 | intron-variant, missense, utr-variant-5-prime | Rnf185 | GRCm38.p3 | 11:3438267 | AGAGGAGGATACACA[C/T]ACAGCACAACAGGCA | 193670 |
rs26914000 | snp | C/T | 0.124444 | 0.216185 | intron-variant, missense, utr-variant-5-prime | Rnf185 | Mm_Celera | 11:3438228 | CTTGGCGTTGATTGA[C/T]AGGTCTGCAGAACAT | 193670 |
rs26914001 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Rnf185 | Mm_Celera | 11:3438145 | CTGTTCTTGAGTCCT[C/T]ATAGGCTCCCTATGT | 193670 |
rs26914002 | snp | C/G | 0.297521 | 0.245442 | intron-variant | Rnf185 | Mm_Celera | 11:3438044 | TGGTCTCAAATATAG[C/G]ACTAAAGACATGCAT | 193670 |
rs26914003 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Rnf185 | Mm_Celera | 11:3437770 | ATCTGTTCACCCCAG[A/G]AACTGAACAGTGAGA | 193670 |
rs26914004 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Rnf185 | Mm_Celera | 11:3436890 | ACCCACTCATGCAGC[A/G]CACAATTCTCCACTG | 193670 |
rs26914005 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Rnf185 | Mm_Celera | 11:3435793 | CCTACAGAGCAAAAA[A/C]ATGTAGCCACAGCCT | 193670 |
rs26914006 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Rnf185 | Mm_Celera | 11:3435686 | GGGTTCCAAAGCCAT[A/C]TACTCATCTATGAAG | 193670 |
rs26914007 | snp | C/T | 0.359862 | 0.224567 | intron-variant | Rnf185 | GRCm38.p3 | 11:3435569 | TCTCCAGGCCTCATC[C/T]AAGTAGGCGCTCAGA | 193670 |
rs26914008 | snp | A/G | 0.32 | 0.24 | intron-variant | Rnf185 | Mm_Celera | 11:3435541 | TCCCACACCACTCTT[A/G]TCCTGACTCCCTTCT | 193670 |
rs26914009 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rnf185 | Mm_Celera | 11:3435362 | CCCGATCCAACAAGG[C/T]TCTGCATGGCTCATG | 193670 |
rs26914010 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Rnf185 | Mm_Celera | 11:3435310 | ATGTAGGAGGGGCTA[C/T]TGCCACATATGCAAT | 193670 |
rs26914011 | snp | G/T | 0.18 | 0.24 | intron-variant | Rnf185 | Mm_Celera | 11:3434357 | TTTGTTGGGTTATAA[G/T]CTTATCATGTAACTT | 193670 |
rs26914012 | snp | G/T | 0.336735 | 0.234472 | intron-variant | Rnf185 | Mm_Celera | 11:3433820 | CTCACCACTGGGGTA[G/T]CAGATCACCTTGACT | 193670 |
rs26914013 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rnf185 | Mm_Celera | 11:3433535 | AAGGCTGGTCACCAA[C/T]TGCCAGTGAAAAACA | 193670 |
rs26914014 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Rnf185 | Mm_Celera | 11:3433467 | TTAGTGTGGGTTTGA[A/G]ACCAGGACTCATGGT | 193670 |
rs26914015 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Rnf185 | Mm_Celera | 11:3433290 | TTCTGCCAGCTGGAT[A/G]CCACTTACCTTATTT | 193670 |
rs26914016 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Rnf185 | Mm_Celera | 11:3432738 | TGAACTGGGAGCTGA[C/T]TTCCCAGAGGGCGGC | 193670 |
rs26914017 | snp | C/G | 0.260355 | 0.249785 | intron-variant | Rnf185 | Mm_Celera | 11:3432716 | AGCTATAAACTCTAA[C/G]TATGATTGAACTGGG | 193670 |
rs26914018 | snp | A/G | 0.32 | 0.24 | intron-variant | Rnf185 | Mm_Celera | 11:3432278 | GGTCTGAGAGCATCA[A/G]GAATCAAAATGAGTG | 193670 |
rs26914019 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Rnf185 | Mm_Celera | 11:3432123 | CAAGCGAGCCTTGCT[C/T]AAGTGGCAGTACACG | 193670 |
rs26914020 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Rnf185 | Mm_Celera | 11:3431777 | ATCAACTCCCCACTA[C/T]TCCACATCCACCTAA | 193670 |
rs26914021 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Rnf185 | Mm_Celera | 11:3431013 | AGGACTCCACTAGAG[C/T]TCGCTCAAATGCTGT | 193670 |
rs26914022 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Rnf185 | Mm_Celera | 11:3429525 | GGTTTACAGCCTCCT[C/T]AGGCTCACAAGTGAT | 193670 |
rs26914023 | snp | A/C | 0.244898 | 0.249948 | intron-variant | Rnf185 | Mm_Celera | 11:3428650 | TTATCAAGTCCAATC[A/C]ATCTGTAAATGGTCA | 193670 |
rs26914024 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Rnf185 | Mm_Celera | 11:3427741 | AAGACTTCAGAGATA[C/T]GGAAGTAGCAGCATT | 193670 |
rs26914025 | snp | A/C/T | 0.132653 | 0.220748 | intron-variant | Rnf185 | Mm_Celera | 11:3426899 | TACCAGTAATTAAAC[A/C/T]GGCTTCTTTCTCTGT | 193670 |
rs26914026 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Rnf185 | Mm_Celera | 11:3426711 | ACATAAGAATGAACC[A/G]AAGCTGCCCTGCCAT | 193670 |
rs26914027 | snp | A/C | 0.277778 | 0.248452 | intron-variant | Rnf185 | Mm_Celera | 11:3426387 | CCAGCAAGTGGGAGC[A/C]TGGCTCTTCTACTCT | 193670 |
rs26914028 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Rnf185 | Mm_Celera | 11:3426300 | GCTTCCCGGGCTGCA[A/G]GAAGTGCTTTCACAA | 193670 |
rs26914029 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Rnf185 | Mm_Celera | 11:3426103 | TGTTAATAGACAGGA[A/G]TTATGGAATCAGGTG | 193670 |
rs26914030 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Rnf185 | Mm_Celera | 11:3425833 | CAGTACTGACACTGC[A/G]ACAGTTTCCACTCTT | 193670 |
rs26914031 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Rnf185 | Mm_Celera | 11:3425773 | CAGACCCGCCCAATG[A/G]TTTGATGAATGTTTA | 193670 |
rs26914032 | snp | A/C | 0.18 | 0.24 | intron-variant | Rnf185 | Mm_Celera | 11:3424538 | TAAATTACCACTGCT[A/C]TAGTAATTACCAGAG | 193670 |
rs26914033 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Rnf185 | Mm_Celera | 11:3424397 | ACATTAGGTCTGTAC[A/G]ACTCAACAGCCACCG | 193670 |
rs26914034 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Rnf185 | Mm_Celera | 11:3422477 | GCAGAGCGTAAGAAG[A/G]TAAAGGGAGACTATC | 193670 |
rs26914035 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Rnf185 | Mm_Celera | 11:3422383 | TAGGATCCAGAGGAG[C/T]GCCCTCAGCCACCAA | 193670 |
rs26914036 | snp | A/T | 0.244898 | 0.249948 | intron-variant | Rnf185 | Mm_Celera | 11:3422210 | GATTAATAAGCCAGA[A/T]ATTCCCTGAAATAAA | 193670 |
rs26914037 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Rnf185 | Mm_Celera | 11:3422158 | CTTAGGGCACTAGCC[A/G]TTGCAAACTGGAACG | 193670 |
rs26914038 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Rnf185 | Mm_Celera | 11:3421944 | TGCACAGCTTACAAA[C/T]TCTTCTCCATCCTTT | 193670 |
rs26914039 | snp | A/C | 0.21875 | 0.248039 | intron-variant | Rnf185 | Mm_Celera | 11:3419739 | GTGTGGCAATCTGCA[A/C]AGAACTTAAGGGATT | 193670 |
rs26914040 | snp | A/G | 0.297521 | 0.245442 | intron-variant | Rnf185 | Mm_Celera | 11:3419719 | GTGCTCAGATCATTG[A/G]ATAAGTGTGGCAATC | 193670 |
rs26914041 | snp | C/G | 0.32 | 0.24 | intron-variant | Rnf185 | Mm_Celera | 11:3419649 | AGTACAGGTGATGAG[C/G]CCCTCTGTTTGTAAT | 193670 |
rs26914042 | snp | C/T | 0.345679 | 0.230967 | intron-variant | Rnf185 | Mm_Celera | 11:3418935 | GATCCAGTCTGAAAG[C/T]TGGACCAGGGTGGAA | 193670 |
rs26914043 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Rnf185 | Mm_Celera | 11:3418886 | AAGGAAAACTGATCA[A/G]GAGCCCAGCCTGGCT | 193670 |
rs26914044 | snp | C/T | 0.165289 | 0.235211 | intron-variant | Rnf185 | Mm_Celera | 11:3418855 | CTCAGCTGTGCAAAC[C/T]GTACCAAGCATGACA | 193670 |
rs26914045 | snp | A/G | 0.18 | 0.24 | intron-variant | Rnf185 | Mm_Celera | 11:3418640 | AGACCATAAGGGCCC[A/G]TACATGAACACTGTT | 193670 |
rs26914046 | snp | A/G | 0.32 | 0.24 | intron-variant | Rnf185 | Mm_Celera | 11:3418343 | CAGGAGAAACACACA[A/G]GGAGAGAGCCCCTGT | 193670 |
rs26914047 | snp | G/T | 0.21875 | 0.248039 | intron-variant | Rnf185 | Mm_Celera | 11:3418277 | ATACTACAATGAGGC[G/T]TTGATCTTCAAAAGA | 193670 |
rs26914048 | snp | C/T | 0.5 | 0 | intron-variant | Rnf185 | Mm_Celera | 11:3418138 | CTATAGCTGTGAATG[C/T]TGCCCCTTGGGGCCA | 193670 |
rs26914049 | snp | C/G | 0.165289 | 0.235211 | utr-variant-3-prime, nc-transcript-variant | Rnf185 | Mm_Celera | 11:3417777 | GACTTCACACTGCCA[C/G]CCATGAGAGGAGATT | 193670 |
rs26914050 | snp | A/T | 0.46875 | 0.121031 | utr-variant-3-prime, nc-transcript-variant | Rnf185 | Mm_Celera | 11:3416994 | GAAGACTAAGGAATG[A/T]CGACCACACTGTATC | 193670 |
rs26914051 | snp | A/C | 0.345679 | 0.230967 | utr-variant-3-prime, nc-transcript-variant | Rnf185 | GRCm38.p3 | 11:3416919 | TCCTGCCTGTCAACA[A/C]AATCCCACAATCAGA | 193670 |
rs26914052 | snp | C/T | 0.444444 | 0.157135 | utr-variant-3-prime, nc-transcript-variant | Rnf185 | GRCm38.p3 | 11:3416808 | GGTCCAGTAGACGCT[C/T]ATCTTGCTGCCCTGC | 193670 |
rs26914053 | snp | C/G | 0.444444 | 0.157135 | utr-variant-3-prime, nc-transcript-variant | Rnf185 | Mm_Celera | 11:3416293 | CTACTGCATGCCCTG[C/G]GATGACTCTGCTGCT | 193670 |
rs26914054 | snp | A/G | 0.408163 | 0.193609 | utr-variant-3-prime, nc-transcript-variant | Rnf185 | GRCm38.p3 | 11:3416029 | ACTTTCACAACAGTG[A/G]AAATCAGTGGCTGGT | 193670 |
rs26914055 | snp | A/C | 0.277778 | 0.248452 | utr-variant-3-prime, nc-transcript-variant | Rnf185 | Mm_Celera | 11:3415983 | CTCCACACTCACAGT[A/C]ATGTAAAACCATTTA | 193670 |
rs29396210 | snp | C/T | 0.375 | 0.216506 | intron-variant | Rnf185 | Mm_Celera | 11:3440206 | ATACATGTGGGCAAA[C/T]ACTCATACACATAAG | 193670 |
rs29406931 | snp | C/T | 0.375 | 0.216506 | intron-variant | Rnf185 | Mm_Celera | 11:3421290 | TGAAGACAGCTATTA[C/T]GTACTTACATATAAT | 193670 |
rs29426535 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rnf185 | GRCm38.p3 | 11:3444421 | AATTAGCCAATTAAG[A/G]AGACTTTCTAAGAGT | 193670 |
rs29447101 | snp | A/G | 0.32 | 0.24 | intron-variant | Rnf185 | Mm_Celera | 11:3438750 | CTGGCCTCGAACTTA[A/G]AAATCCGCCTGCCTC | 193670 |
rs29448475 | snp | C/G | 0.375 | 0.216506 | intron-variant | Rnf185 | GRCm38.p3 | 11:3444412 | GCTGACAAGAATTAG[C/G]CAATTAAGAAGACTT | 193670 |
rs29483907 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Rnf185 | Mm_Celera | 11:3449676 | GCATTACAACACTAA[A/G]AAAGGGTAATGGTGC | 193670 |
rs45780304 | snp | C/T | | | intron-variant | Rnf185 | Mm_Celera | 11:3422433 | CTGAGGCCTCGGATT[C/T]CTGTTGCTTGCTAAT | 193670 |
rs47708132 | snp | A/G | | | intron-variant | Rnf185 | Mm_Celera | 11:3423210 | ATGATAAAACAATAA[A/G]AAGCTAGAATATGAA | 193670 |
rs49680402 | snp | A/G | | | intron-variant | Rnf185 | Mm_Celera | 11:3423227 | AGCTAGAATATGAAC[A/G]AACACCCCTCTAAAA | 193670 |
rs49982380 | snp | A/C | | | intron-variant | Rnf185 | Mm_Celera | 11:3423314 | ATGAAATATACTCCC[A/C]AAGTTTAATTTGAAA | 193670 |
rs50160297 | snp | A/G | | | intron-variant | Rnf185 | Mm_Celera | 11:3423200 | ACATAAATAAATGAT[A/G]AAACAATAAAAAGCT | 193670 |
rs50902657 | snp | G/T | | | intron-variant | Rnf185 | Mm_Celera | 11:3422428 | GCTTCCTGAGGCCTC[G/T]GATTTCTGTTGCTTG | 193670 |
rs52534608 | snp | A/G | | | intron-variant | Rnf185 | Mm_Celera | 11:3444129 | AAGAAAGAAAGAAAG[A/G]AAGGAAGGGAAGAAA | 193670 |
rs211704796 | snp | A/C | | | intron-variant | Rnf185 | Mm_Celera | 11:3443122 | TTGCCTTGAGGTAAA[A/C]ATTACTACAACACTG | 193670 |
rs211788068 | snp | A/T | | | intron-variant | Rnf185 | Mm_Celera | 11:3444852 | GGAAAGTCTCTAACA[A/T]CAACTTTTACAAACC | 193670 |
rs211788836 | snp | C/T | | | intron-variant | Rnf185 | Mm_Celera | 11:3433453 | AGCTGGCTGAGTGAT[C/T]AGTGTGGGTTTGAGA | 193670 |
rs211942007 | in-del | -/A | | | upstream-variant-2KB, intron-variant | Rnf185, 8430429K09Rik | Mm_Celera | 11:3453858 | ACTCAAAGGAAGCTC[-/A]AGGACAACTTTATTA | 193670 |
rs211978307 | snp | C/T | | | upstream-variant-2KB, intron-variant | Rnf185, 8430429K09Rik | Mm_Celera | 11:3454415 | CAAAACATTCATACA[C/T]ATAAAAAAACAAAAC | 193670 |
rs212094876 | in-del | -/AAACTAG | | | intron-variant | Rnf185 | Mm_Celera | 11:3422339 | CACAAGCAAGCAAGC[-/AAACTAG]ATTAGTAGCAGCTGC | 193670 |
rs212123718 | in-del | -/TTTTTCTTTTTCT | | | intron-variant | Rnf185 | GRCm38.p3 | 11:3430660 | TTCTTTTTCTTTTTC[-/TTTTTCTTTTTCT]TTTTTTTTTTTTTTT | 193670 |
rs212303097 | snp | C/T | | | intron-variant | Rnf185 | Mm_Celera | 11:3423267 | AAAAAGATAACACAA[C/T]GACATTTTAAAGATA | 193670 |
rs212314645 | in-del | -/ACACACACACACACAC | | | intron-variant | Rnf185 | Mm_Celera | 11:3441459 | TAGCACTTTACACTT[-/ACACACACACACACAC]ACACACACACACACA | 193670 |
rs212386929 | in-del | -/GAAAGAAAGAAAGAAA | | | intron-variant | Rnf185 | Mm_Celera | 11:3422242 | CATCAAAAGAAAAAT[-/GAAAGAAAGAAAGAAA]GAAAGAAAGAAAGAA | 193670 |
rs212444905 | snp | C/T | | | intron-variant | Rnf185 | Mm_Celera | 11:3421855 | TTGAACAAAGGTCAC[C/T]AGGCTTGCGTGAAAA | 193670 |
rs212448051 | in-del | -/CC | | | intron-variant | Rnf185 | Mm_Celera | 11:3430511 | AAAAACAAAAAAAAA[-/CC]CCCAAAGCAAACAAC | 193670 |
rs212466065 | in-del | -/CTTTTTCTTTTTC | | | intron-variant | Rnf185 | GRCm38.p3 | 11:3430659 | CTTCTTTTTCTTTTT[-/CTTTTTCTTTTTC]TTTTTTTTTTTTTTT | 193670 |
rs212470820 | snp | A/G | | | intron-variant | Rnf185 | Mm_Celera | 11:3426111 | GACAGGAATTATGGA[A/G]TCAGGTGAAATGCCA | 193670 |
rs212585257 | snp | A/C | | | intron-variant | Rnf185 | Mm_Celera | 11:3436575 | TCCACTCTACATTTA[A/C]ATTTAAGTTTTATTT | 193670 |
rs212701868 | snp | A/C | | | intron-variant | Rnf185 | Mm_Celera | 11:3434439 | GGTAGATCACTCCAG[A/C]GGAAGGACACTCACA | 193670 |
rs212726635 | snp | C/T | | | intron-variant | Rnf185 | Mm_Celera | 11:3446770 | AACTAGTCTAGACAA[C/T]CTATTAAGACCCAAT | 193670 |