SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs3693558 | snp | C/T | 0.5 | 0 | intron-variant | Rnf157 | Mm_Celera | 11:116364620 | GATCCTAATATACTG[C/T]AGACACTTAGGAACC | 217340 |
rs3693734 | snp | C/T | 0.5 | 0 | intron-variant | Rnf157 | Mm_Celera | 11:116364708 | AACATTTTACTACAA[C/T]TATAGGTGTTTTGTT | 217340 |
rs3696047 | snp | G/T | 0.5 | 0 | intron-variant | Rnf157 | Mm_Celera | 11:116365034 | ATTTTTGTTTTCAAT[G/T]TTTTTTATTACATTT | 217340 |
rs4135890 | snp | C/G | 0.5 | 0 | intron-variant | Rnf157 | Mm_Celera | 11:116364932 | TCACTCTGTAGACCA[C/G]GCTGGCCTTGAGCTC | 217340 |
rs4135922 | snp | A/G | 0.5 | 0 | intron-variant | Rnf157 | GRCm38.p3 | 11:116364944 | CCACGCTGGCCTTGA[A/G]CTCAAATCCGTCTGC | 217340 |
rs6163168 | snp | C/T | 0.5 | 0 | intron-variant | Rnf157 | Mm_Celera | 11:116361108 | CTATTGGCATGGTTG[C/T]GCCATCTCAGTGTGG | 217340 |
rs6163684 | snp | A/G | 0.5 | 0 | intron-variant | Rnf157 | Mm_Celera | 11:116361194 | AGTGTGGCTATTGGC[A/G]TGGTTGTGCCATCTC | 217340 |
rs6164149 | snp | C/T | 0.5 | 0 | intron-variant | Rnf157 | Mm_Celera | 11:116361288 | CAGGCTGAGTGCGTA[C/T]GCCAGAACATGGTTC | 217340 |
rs6222661 | snp | C/T | 0.5 | 0 | intron-variant | Rnf157 | Mm_Celera | 11:116382436 | TCTCATGTCATGTCA[C/T]AGCTGCAGGACAGGT | 217340 |
rs6234371 | snp | C/T | 0.5 | 0 | intron-variant | Rnf157 | GRCm38.p3 | 11:116409518 | aggcgtgatccacca[C/T]gccaggcTAgtttgg | 217340 |
rs6234931 | snp | A/G | 0.5 | 0 | intron-variant | Rnf157 | Mm_Celera | 11:116409630 | gtgctagagttaaag[A/G]TTTCTAATCACAGAT | 217340 |
rs6235575 | snp | A/C | 0.5 | 0 | intron-variant | Rnf157 | Mm_Celera | 11:116409791 | GCCTGTGTGACTCTG[A/C]ATTCTTATAATTGTT | 217340 |
rs6248513 | snp | C/T | 0.5 | 0 | intron-variant | Rnf157 | Mm_Celera | 11:116409813 | ATAATTGTTCGTGTA[C/T]ACAACTTACCTCTGA | 217340 |
rs6248544 | snp | A/G | 0.5 | 0 | intron-variant | Rnf157 | GRCm38.p3 | 11:116409841 | TGACACTAAATGATT[A/G]GCACTGAACTTTTTG | 217340 |
rs6312369 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Rnf157 | Mm_Celera | 11:116387377 | TAAATCCTACAGACC[C/G]GGGGAGCCAGGAANT | 217340 |
rs6312801 | snp | A/G | 0.46875 | 0.121031 | intron-variant | Rnf157 | GRCm38.p3 | 11:116387391 | CNGGGGAGCCAGGAA[A/G]TCTGTGGCATTTATA | 217340 |
rs6317955 | snp | C/G | 0.489796 | 0.070696 | intron-variant | Rnf157 | GRCm38.p3 | 11:116381998 | GTATATTAATTGAGC[C/G]CCAATTAAAGAGCTA | 217340 |
rs6318331 | snp | A/G | 0.5 | 0 | intron-variant | Rnf157 | Mm_Celera | 11:116382031 | GGTGAggagctgaag[A/G]gatgacttggctgtt | 217340 |
rs6318462 | snp | C/T | 0.5 | 0 | intron-variant | Rnf157 | Mm_Celera | 11:116382097 | tccccagcactcaga[C/T]ggtgcctcgtaactg | 217340 |
rs6319967 | snp | A/G | 0.5 | 0 | intron-variant | Rnf157 | Mm_Celera | 11:116382315 | TATCAGGACAGGAGA[A/G]CACTGCAGGACAGCC | 217340 |
rs6347770 | snp | C/G | 0.489796 | 0.070696 | intron-variant | Rnf157 | GRCm38.p3 | 11:116396145 | CAGGGCTGGGTGCAC[C/G]GGTCACTGTAGGCCC | 217340 |
rs6348393 | snp | A/T | 0.5 | 0 | intron-variant | Rnf157 | Mm_Celera | 11:116362893 | GTTTGTTAACCCTGA[A/T]CCTACAGGCACCTGG | 217340 |
rs6349511 | snp | A/G | 0.5 | 0 | intron-variant | Rnf157 | Mm_Celera | 11:116363082 | GGGCAATAGTGATTC[A/G]AGNATCTACCAACAT | 217340 |
rs6349519 | snp | A/G | 0.5 | 0 | intron-variant | Rnf157 | Mm_Celera | 11:116363085 | CAATAGTGATTCNAG[A/G]ATCTACCAACATGCA | 217340 |
rs6369059 | snp | C/T | 0.5 | 0 | intron-variant | Rnf157 | Mm_Celera | 11:116357839 | ctgttctcagactca[C/T]agagatgcacctgcc | 217340 |
rs6369104 | snp | A/C | 0.5 | 0 | intron-variant | Rnf157 | Mm_Celera | 11:116357866 | tgcctctgtctgcca[A/C]gtgctggaattaaag | 217340 |
rs6369182 | snp | C/T | 0.5 | 0 | intron-variant | Rnf157 | Mm_Celera | 11:116357911 | ATCTGGTTTGGTCAC[C/T]ACTTTTTTCAAACCA | 217340 |
rs26979019 | snp | G/T | 0.391111 | 0.206368 | intron-variant | Rnf157 | Mm_Celera | 11:116374065 | ACTCCTTGCCTGCCA[G/T]TAGGATGCCAAGCTT | 217340 |
rs26979020 | snp | G/T | 0.391111 | 0.206368 | intron-variant | Rnf157 | Mm_Celera | 11:116374034 | GCTTTTCTCCACGGC[G/T]CTGCTTCTCTGACTG | 217340 |
rs26979021 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Rnf157 | Mm_Celera | 11:116373987 | ACCCCTTGAGCCACA[C/T]GCTTCAATGCCACCA | 217340 |
rs26979022 | snp | C/T | 0.426035 | 0.177515 | intron-variant | Rnf157 | Mm_Celera | 11:116373861 | GTCAGAGACAAAATC[C/T]AGACCTCCCAACCCA | 217340 |
rs27002462 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Rnf157 | Mm_Celera | 11:116412164 | CCAGCCATCTCCTTG[A/C]CAGAAACTAGGAAAG | 217340 |
rs27002463 | snp | A/G | 0.396694 | 0.202437 | intron-variant | Rnf157 | Mm_Celera | 11:116412021 | TCGCCAGCAGCTTGA[A/G]CAGCAGTCCTCACTC | 217340 |
rs27002464 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Rnf157 | GRCm38.p3 | 11:116411820 | GCATGTCTTTATTCT[A/G]CCAAGAGAGAATGGG | 217340 |
rs27002465 | snp | C/T | 0.473373 | 0.11227 | intron-variant | Rnf157 | GRCm38.p3 | 11:116411738 | AGGGAGGCAGGTTCA[C/T]TGTCTGGTCCCAGCT | 217340 |
rs27002466 | snp | C/G | 0.32 | 0.24 | intron-variant | Rnf157 | Mm_Celera | 11:116411095 | TTCTCCTGAGGCAGC[C/G]GACTCTCTCACAAAC | 217340 |
rs27002467 | snp | A/G | 0.18 | 0.24 | intron-variant | Rnf157 | Mm_Celera | 11:116409211 | TGGTCAGAATCACAC[A/G]TCCACTATGCTCATT | 217340 |
rs27002468 | snp | C/T | 0.42 | 0.183303 | intron-variant | Rnf157 | Mm_Celera | 11:116407613 | AGAAATCCTTTACTG[C/T]AGGCATGACTTGAAA | 217340 |
rs27002469 | snp | C/T | 0.32 | 0.24 | intron-variant | Rnf157 | Mm_Celera | 11:116403703 | CTAAAATGTTCTCAA[C/T]TGGATTCGTGGTAAT | 217340 |
rs27002470 | snp | A/G | 0.32 | 0.24 | intron-variant | Rnf157 | Mm_Celera | 11:116403020 | TTTCCACACAAGCTC[A/G]GTGGAAGACGGCAGC | 217340 |
rs27002471 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Rnf157 | Mm_Celera | 11:116400734 | CCTCGGGGCACAAAC[C/T]TGTCTGGCTTTTCCT | 217340 |
rs27002472 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Rnf157 | Mm_Celera | 11:116400723 | AGGGCGTGCAGCCTC[C/G]GGGCACAAACCTGTC | 217340 |
rs27002473 | snp | C/T | 0.32 | 0.24 | intron-variant | Rnf157 | Mm_Celera | 11:116400558 | AAGAAGCATCAGAAG[C/T]GAAGAGAGACTGTGT | 217340 |
rs27002474 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Rnf157 | Mm_Celera | 11:116400531 | CCCAGTGACTGAAGA[A/C]AGACTGTGGCTAAGA | 217340 |
rs27002475 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Rnf157 | Mm_Celera | 11:116400250 | TGGCCAATAACACAC[A/T]GACTAAAATGATTTT | 217340 |
rs27002476 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Rnf157 | GRCm38.p3 | 11:116400143 | AGACACATAGTAAGC[A/G]CCATCAGGAGGATCA | 217340 |
rs27002477 | snp | A/G | 0.32 | 0.24 | intron-variant | Rnf157 | Mm_Celera | 11:116399795 | TTAAAATCAAGGGCT[A/G]TCTAATGTGGCGGAA | 217340 |
rs27002478 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rnf157 | Mm_Celera | 11:116399216 | CCCTAGGCATCAGGG[C/T]AAGCAGGCGGCAGGG | 217340 |
rs27002479 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Rnf157 | Mm_Celera | 11:116399155 | GACTGATTGGTTTAC[A/G]TAGCACAGTGATCTA | 217340 |
rs27002480 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Rnf157 | Mm_Celera | 11:116398881 | AGGGTGGTTTGTCCC[A/T]GTAAGGAATGTTAAG | 217340 |
rs27002481 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rnf157 | Mm_Celera | 11:116398811 | ATGGTCCTGGGCCTA[C/T]GCTCAGCACTGCAAA | 217340 |
rs27002482 | snp | C/G | 0.32 | 0.24 | intron-variant | Rnf157 | Mm_Celera | 11:116398487 | CATGCTGCACACTTC[C/G]CTGGCCCTATTTTCC | 217340 |
rs27002483 | snp | A/C | 0.32 | 0.24 | intron-variant | Rnf157 | Mm_Celera | 11:116398430 | CTGCCACAGCGCAGC[A/C]CGCAACGCGCCCCAG | 217340 |
rs27002484 | snp | C/T | 0.32 | 0.24 | intron-variant | Rnf157 | Mm_Celera | 11:116398190 | GGGAGAAGACAGATG[C/T]AACAGAAAACAGAAC | 217340 |
rs27002485 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Rnf157 | Mm_Celera | 11:116398164 | CTAGAGAGAAGCCAC[A/T]GGAAGGGAGAGGGAG | 217340 |
rs27002486 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Rnf157 | Mm_Celera | 11:116398105 | AGCCGGGATTTTTGA[A/G]ATTCTTTTCAGTGAG | 217340 |
rs27002487 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Rnf157 | Mm_Celera | 11:116398069 | GTGTAATCCAGCTGG[A/G]GTAAATATAAACTTG | 217340 |
rs27002488 | snp | A/T | 0.32 | 0.24 | intron-variant | Rnf157 | Mm_Celera | 11:116398029 | CAAATTAACGCAAAG[A/T]ACTTAGGAACCCACA | 217340 |
rs27002489 | snp | A/G | 0.32 | 0.24 | intron-variant | Rnf157 | Mm_Celera | 11:116396439 | GCTTCTGATTTCAGA[A/G]CCTGGCACAAAATCA | 217340 |
rs27002490 | snp | A/G | 0.32 | 0.24 | intron-variant | Rnf157 | Mm_Celera | 11:116396395 | AGAAAGGAAGAGGTT[A/G]GGGCTCCCAACAAAG | 217340 |
rs27002491 | snp | A/T | 0.336735 | 0.234472 | intron-variant | Rnf157 | Mm_Celera | 11:116396123 | ACATCAGCAAACTTG[A/T]TTTTAACAGGGCTGG | 217340 |
rs27002492 | snp | A/C | 0.260355 | 0.249785 | intron-variant | Rnf157 | Mm_Celera | 11:116395740 | GGCCTTCCTCTGCAC[A/C]CTGACAGCTGTTTTA | 217340 |
rs27002493 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Rnf157 | Mm_Celera | 11:116395244 | CTGGACCAGGCACAC[A/G]GTCTCTATATGCCAG | 217340 |
rs27002494 | snp | C/T | 0.375 | 0.216506 | intron-variant | Rnf157 | Mm_Celera | 11:116395063 | AGAACTCAGTCACTG[C/T]AGACCTTCTCTCTTA | 217340 |
rs27002495 | snp | A/G | 0.32 | 0.24 | intron-variant | Rnf157 | Mm_Celera | 11:116395015 | AGCACCCAAGCAATC[A/G]TTGGCAGCACTCACT | 217340 |
rs27002496 | snp | C/T | 0.375 | 0.216506 | intron-variant | Rnf157 | Mm_Celera | 11:116394942 | CCCTCTAGGTGAGAG[C/T]CCTTTCCCACCAGCC | 217340 |
rs27002497 | snp | C/T | 0.35503 | 0.226867 | intron-variant | Rnf157 | Mm_Celera | 11:116389326 | GATGAGAGCCAGCAT[C/T]GGCAACCTTCCTGAA | 217340 |
rs27002498 | snp | C/T | 0.375 | 0.216506 | intron-variant | Rnf157 | Mm_Celera | 11:116389303 | AGGAGAGGGGTCACC[C/T]GGGACAGGATGAGAG | 217340 |
rs27002499 | snp | G/T | 0.244898 | 0.249948 | intron-variant | Rnf157 | Mm_Celera | 11:116389018 | GAGGAGCTCAGTCAC[G/T]CAGGGTCCTGCACGG | 217340 |
rs27002500 | snp | A/C | 0.244898 | 0.249948 | intron-variant | Rnf157 | Mm_Celera | 11:116388910 | GGTACTACAGAAACC[A/C]ACATACCAACAAGAA | 217340 |
rs27002501 | snp | C/T | 0.165289 | 0.235211 | intron-variant | Rnf157 | Mm_Celera | 11:116387946 | CTCTGTGGCTCTGTG[C/T]GCCTGCTGAATGAGC | 217340 |
rs27002502 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Rnf157 | Mm_Celera | 11:116387922 | CCTGGCAGGCTTGGT[A/G]ATATTCAACTCTGTG | 217340 |
rs27002503 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Rnf157 | Mm_Celera | 11:116387882 | GAGGCTCTGAAGCAC[A/G]GTGAGGTCAGAAGCT | 217340 |
rs27002504 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Rnf157 | Mm_Celera | 11:116387813 | CACAAGGGTTCCTGG[A/G]CAGAATGTGGGAAAG | 217340 |
rs27002505 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Rnf157 | Mm_Celera | 11:116387787 | ACCTACAAAGTGCTC[C/T]TGGTGATCCACACAA | 217340 |
rs27002506 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Rnf157 | Mm_Celera | 11:116387549 | TAACTTGATGCTCAC[A/G]AGCAGACACCCAGCG | 217340 |
rs27002508 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Rnf157 | Mm_Celera | 11:116387227 | TCATTCATGCAAATC[C/T]AACCCTGAGAGCTGA | 217340 |
rs27002509 | snp | C/G | 0.391111 | 0.206368 | intron-variant | Rnf157 | GRCm38.p3 | 11:116387086 | TCAAGTCAGCACCAT[C/G]CCTGCTTTATAAGTG | 217340 |
rs27002510 | snp | G/T | 0.297521 | 0.245442 | intron-variant | Rnf157 | Mm_Celera | 11:116387066 | TTCCAAGCACTGCAC[G/T]CCTCTCAAGTCAGCA | 217340 |
rs27002511 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Rnf157 | GRCm38.p3 | 11:116387054 | TCTGAAGGCATCTTC[C/G]AAGCACTGCACTCCT | 217340 |
rs27002512 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Rnf157 | Mm_Celera | 11:116380773 | CTGGTCGGTTTGATG[C/T]CTCTGGAACAGGAGG | 217340 |
rs27002513 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Rnf157 | Mm_Celera | 11:116380716 | TTCTGTGAATTTCCC[A/T]GCAAGGTGAAGGGAG | 217340 |
rs27002514 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Rnf157 | GRCm38.p3 | 11:116380695 | GGTGATAGCTGGTCC[C/T]TGGCATTCTGTGAAT | 217340 |
rs27002515 | snp | A/G | 0.32 | 0.24 | intron-variant | Rnf157 | Mm_Celera | 11:116380444 | ACCCTGTGTGGCAGA[A/G]TCTGGTGGTGGTCAG | 217340 |
rs27002516 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Rnf157 | Mm_Celera | 11:116380141 | TTTTCAATTACATGT[A/C]TATGGAGCTGACTCT | 217340 |
rs27002517 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Rnf157 | Mm_Celera | 11:116379898 | ATTCTTTCCCCAGTA[C/T]AAGCGGCACACTATT | 217340 |
rs27002518 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Rnf157 | Mm_Celera | 11:116379762 | CTGAACCCAGATAAA[A/C]TGCGCGTCACTTCCT | 217340 |
rs27002519 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Rnf157 | Mm_Celera | 11:116379754 | TGGCAAGACTGAACC[C/T]AGATAAACTGCGCGT | 217340 |
rs27002520 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Rnf157 | Mm_Celera | 11:116379304 | AAGTCCTGCCTACAT[A/G]AGACCCTGCCAACAA | 217340 |
rs27002521 | snp | A/G | 0.429688 | 0.173817 | intron-variant | Rnf157 | GRCm38.p3 | 11:116379192 | TCTTCTTCTGTGGTG[A/G]CACACAGGACACAGC | 217340 |
rs27002522 | snp | C/G | 0.277778 | 0.248452 | intron-variant | Rnf157 | Mm_Celera | 11:116379020 | TCATAGGTTGGCTCT[C/G]TGCAGATGACAAGAC | 217340 |
rs27002523 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Rnf157 | Mm_Celera | 11:116379015 | TACCCTCATAGGTTG[G/T]CTCTCTGCAGATGAC | 217340 |
rs27002524 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Rnf157 | Mm_Celera | 11:116378972 | CCCTTCCTGTCACTC[A/G]GGCGATGGCAGCCAA | 217340 |
rs27002525 | snp | A/C/T | 0.231111 | 0.249285 | intron-variant | Rnf157 | Mm_Celera | 11:116378562 | TTACTCTGTTTGAGA[A/C/T]GCAAACTTCCAACAG | 217340 |
rs27002526 | snp | A/G | 0.489796 | 0.070696 | intron-variant | Rnf157 | GRCm38.p3 | 11:116378097 | AAAGGCATGTCACCA[A/G]CGATCAGCAATGGTG | 217340 |
rs27002527 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Rnf157 | GRCm38.p3 | 11:116377573 | AGTACAGACAGAAAT[A/G]TATACTGGCAGTGTG | 217340 |
rs27002528 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rnf157 | Mm_Celera | 11:116377431 | CAGCTTGCCACCTTC[C/T]TAGTGCACCACAACT | 217340 |
rs27002529 | snp | A/C | 0.260355 | 0.249785 | intron-variant | Rnf157 | Mm_Celera | 11:116377308 | AGCCAGATGCTTCAG[A/C]GCTCATCTGCCCAAC | 217340 |
rs27002530 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rnf157 | Mm_Celera | 11:116377245 | GACGGCAACAGGAAG[C/T]GGGTGAGAGTGTCCG | 217340 |
rs27002531 | snp | C/T | 0.32 | 0.24 | intron-variant | Rnf157 | Mm_Celera | 11:116376089 | GGAACTGCCTGTGAG[C/T]TGAGAGAAGTGTCTA | 217340 |