SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs6391298 | snp | C/T | 0.359862 | 0.224567 | intron-variant | Pwp1 | Mm_Celera | 10:85875964 | CTGATCTCGGGAACA[C/T]ATTCTTCAAATTACT | 103136 |
rs6392488 | snp | A/G | 0.5 | 0 | intron-variant | Pwp1 | Mm_Celera | 10:85876205 | TGGTTGGTGATAAAG[A/G]ACACCCAAGCCAAAA | 103136 |
rs13472493 | snp | A/G | | | utr-variant-3-prime | Pwp1 | Mm_Celera | 10:85888609 | tgaattcaggccctc[A/G]tgttggcaaatcaaa | 103136 |
rs13480684 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Pwp1 | Mm_Celera | 10:85872584 | AGTAGTGACAACTCG[A/G]TATGTGATAGACGTG | 103136 |
rs29352869 | snp | C/T | 0.197531 | 0.244432 | intron-variant | Pwp1 | Mm_Celera | 10:85886597 | ATCCCGAATGAATTA[C/T]CTCACTGAGGGGTTT | 103136 |
rs30146185 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Pwp1 | Mm_Celera | 10:85883859 | TTGCCCTGGACTTTG[A/G]AAATAGGATTCATCC | 103136 |
rs30146187 | snp | C/T | 0.32 | 0.24 | intron-variant | Pwp1 | Mm_Celera | 10:85884193 | GCTAGAGAGGTGACT[C/T]GGCTAGTAGGCTCTC | 103136 |
rs30146189 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Pwp1 | Mm_Celera | 10:85884445 | AATAAACGTAACCCT[A/G]GCATGCAATGTGTGC | 103136 |
rs30146191 | snp | C/T | 0.124444 | 0.216185 | synonymous-codon | Pwp1 | Mm_Celera | 10:85884544 | GATCGAGAGAGTGAC[C/T]TGGAACCACTTCTCA | 103136 |
rs30146193 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Pwp1 | Mm_Celera | 10:85885051 | AGGCTTTTCTAAACG[C/T]TCACTAACATCAGCC | 103136 |
rs30147155 | snp | C/G | 0.32 | 0.24 | intron-variant | Pwp1 | Mm_Celera | 10:85885196 | TAAGAACATTAACAG[C/G]TTATTTCCATGTCAC | 103136 |
rs30147157 | snp | C/T | 0.32 | 0.24 | intron-variant | Pwp1 | Mm_Celera | 10:85885217 | TCCATGTCACTCCAC[C/T]GCTATGGCAATATTG | 103136 |
rs30147159 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Pwp1 | Mm_Celera | 10:85885236 | ATGGCAATATTGAGA[C/T]CTGATCTGACCATGC | 103136 |
rs30147161 | snp | A/G | 0.32 | 0.24 | intron-variant | Pwp1 | Mm_Celera | 10:85885570 | CATTGCCACATTGTA[A/G]TGTTCCATACCATCA | 103136 |
rs30147163 | snp | C/G | 0.32 | 0.24 | synonymous-codon | Pwp1 | Mm_Celera | 10:85885633 | AGATGATGGCTTTGT[C/G]TATAACCTGGATGCA | 103136 |
rs30147874 | snp | A/C | 0.32 | 0.24 | intron-variant | Pwp1 | Mm_Celera | 10:85872756 | AGGATAGGGACAACA[A/C]TTGCCTTATTAAAAA | 103136 |
rs30147876 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Pwp1 | Mm_Celera | 10:85872831 | GCTTTCGAAGTATTA[A/G]GAGAGTCTTAAAAAT | 103136 |
rs30147878 | snp | A/C | 0.32 | 0.24 | intron-variant | Pwp1 | Mm_Celera | 10:85873109 | AGATCCACATGCTTG[A/C]TCAACAAAAGCTTTA | 103136 |
rs30147880 | snp | C/T | 0.375 | 0.216506 | intron-variant | Pwp1 | Mm_Celera | 10:85873147 | ACCTCCGGCCTTCCC[C/T]GGAGTTTTTCAGTCT | 103136 |
rs30147882 | snp | G/T | 0.260355 | 0.249785 | intron-variant | Pwp1 | Mm_Celera | 10:85873259 | TTTGGAGACCAGGTC[G/T]CACTCTGTAGCCCGC | 103136 |
rs30148015 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Pwp1 | Mm_Celera | 10:85885716 | GTGAGCACAAATGAC[A/G]CTTCTTTTCAAATGC | 103136 |
rs30148017 | snp | C/T | 0.32 | 0.24 | intron-variant | Pwp1 | Mm_Celera | 10:85886155 | CTGCCTCTGGACATC[C/T]TGGAAGTTGAGGCAC | 103136 |
rs30148019 | snp | A/G | 0.32 | 0.24 | intron-variant | Pwp1 | Mm_Celera | 10:85886305 | TACTGACTAAGAACA[A/G]GTATTGCCTATGTTG | 103136 |
rs30148021 | snp | A/G/T | 0.32 | 0.24 | intron-variant | Pwp1 | Mm_Celera | 10:85886362 | GCAGCACAGTAGAGA[A/G/T]TGTCACAGAAGTTAA | 103136 |
rs30148023 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Pwp1 | Mm_Celera | 10:85886370 | GTAGAGATTGTCACA[A/G]AAGTTAAAGCCATGT | 103136 |
rs30148285 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Pwp1 | Mm_Celera | 10:85875919 | GCTGTGAAGCCTGCC[A/G]TCTAAGTGTTTACCT | 103136 |
rs30148288 | snp | C/T | 0.124444 | 0.216185 | synonymous-codon | Pwp1 | Mm_Celera | 10:85876494 | CACTTAGGAACAATA[C/T]GAGCATGAAGATTTC | 103136 |
rs30148290 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Pwp1 | Mm_Celera | 10:85876592 | TGCACGGTGAGTAAC[A/G]GTTGCCCACTGGGAT | 103136 |
rs30148292 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Pwp1 | Mm_Celera | 10:85876746 | ATGAGTGTTCTGCCT[G/T]AATGTAACTGGGCAT | 103136 |
rs30148846 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Pwp1 | Mm_Celera | 10:85886745 | GAGAACCAACTCCTG[C/T]AGGTGATCTGGCCAC | 103136 |
rs30148848 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Pwp1 | Mm_Celera | 10:85886943 | GCATACATGCAAAGA[G/T]ACTGTTTAAGAAGAA | 103136 |
rs30148850 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Pwp1 | Mm_Celera | 10:85887007 | TGTTTGAAAAGATGA[A/G]TAACGTTTCTGGGTG | 103136 |
rs30148852 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Pwp1 | Mm_Celera | 10:85887102 | CCAGCCTCATGGTTC[A/G]TCCGAAATGCTGCGC | 103136 |
rs30148854 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Pwp1 | Mm_Celera | 10:85873869 | TCCCAGAAAGAATCC[A/G]TTTACATTGGGCAGT | 103136 |
rs30148856 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Pwp1 | Mm_Celera | 10:85873919 | CAGAGGACGGATGTT[A/C]TATGGTTTGATAGCC | 103136 |
rs30148858 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Pwp1 | Mm_Celera | 10:85874064 | GTGAGCACGGCTGCT[A/G]ACAGTGGTAGGTGGG | 103136 |
rs30148860 | snp | A/C | 0.32 | 0.24 | intron-variant | Pwp1 | Mm_Celera | 10:85874097 | GAGTCTGATTTGTAC[A/C]AAGGATTCGTACAGA | 103136 |
rs30148862 | snp | C/T | 0.124444 | 0.216185 | synonymous-codon | Pwp1 | Mm_Celera | 10:85874307 | AGAGGAAGTGAACCG[C/T]CTCATCGCTGAAGCA | 103136 |
rs30149154 | snp | A/G | 0.32 | 0.24 | intron-variant | Pwp1 | Mm_Celera | 10:85876769 | CTGGGCATTCTGTGT[A/G]TGCTTGGTGCCCAAA | 103136 |
rs30149156 | snp | G/T | 0.32 | 0.24 | intron-variant | Pwp1 | Mm_Celera | 10:85876941 | GCTACTTGAGATAGT[G/T]TCCTTCATAGAACAT | 103136 |
rs30149158 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Pwp1 | Mm_Celera | 10:85877203 | TTTGTATGTTTGCCT[A/G]CACGTATGTTTTTGT | 103136 |
rs30149160 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Pwp1 | Mm_Celera | 10:85877383 | ATCATTGTGTTCTGT[C/T]GATATTTGCAAATTT | 103136 |
rs30149162 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Pwp1 | Mm_Celera | 10:85877514 | GAAACAGAATCCATG[C/T]AAAAGAAATGTGGAT | 103136 |
rs30149604 | snp | C/T | 0.231111 | 0.249285 | synonymous-codon | Pwp1 | Mm_Celera | 10:85874518 | GCAGAGTGGCCCGAC[C/T]CAGGCACCGCCTAGG | 103136 |
rs30149606 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Pwp1 | Mm_Celera | 10:85874687 | CCTCTCTTTTACTCT[A/C]CCCAGGGTCGGGTCA | 103136 |
rs30149608 | snp | A/G | 0.32 | 0.24 | intron-variant | Pwp1 | Mm_Celera | 10:85874993 | TGGCAAGGCTGCTCG[A/G]TTAGCACAGGAGGCA | 103136 |
rs30149610 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Pwp1 | Mm_Celera | 10:85875135 | CCATTGTCACTCTGA[G/T]CACGTTAATAAGCTC | 103136 |
rs30149612 | snp | C/T | 0.32 | 0.24 | intron-variant | Pwp1 | Mm_Celera | 10:85875355 | TGGTCTGCAGGAGCA[C/T]GCTGTTCCTCATGTG | 103136 |
rs30149774 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Pwp1 | Mm_Celera | 10:85887421 | AGGCATGTCCAGTGC[A/G]TATCCTGTAATCCTT | 103136 |
rs30149776 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Pwp1 | Mm_Celera | 10:85887532 | GAGCTTCCTAGGAAA[A/G]CTGAAGAAAATGTAG | 103136 |
rs30149778 | snp | C/T | 0.124444 | 0.216185 | missense | Pwp1 | Mm_Celera | 10:85888075 | TCGTTATAGGCGGCA[C/T]GAAAGGTTTATCTGT | 103136 |
rs30149780 | snp | A/G | 0.124444 | 0.216185 | utr-variant-3-prime | Pwp1 | Mm_Celera | 10:85888976 | TAGCAATCTCACACC[A/G]CCTCACAGAAAGGCT | 103136 |
rs30149782 | snp | A/G | 0.142012 | 0.225474 | downstream-variant-500B | Pwp1 | Mm_Celera | 10:85889330 | TTAAAAACTACCCTC[A/G]CTCCTGTCGTGCTTT | 103136 |
rs30150024 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Pwp1 | Mm_Celera | 10:85877661 | CGTGCCTTCTCAGCA[A/G]ATAGAACATGACGTG | 103136 |
rs30150026 | snp | A/C | 0.142012 | 0.225474 | intron-variant | Pwp1 | Mm_Celera | 10:85877799 | AGGTAGAACTTGCTT[A/C]TTGGGTTTTCTTAGT | 103136 |
rs30150028 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Pwp1 | Mm_Celera | 10:85877838 | GCTCCTTAACTTTCT[A/G]TGTCCATGAATGTTG | 103136 |
rs30150030 | snp | C/T | 0.426035 | 0.177515 | intron-variant | Pwp1 | Mm_Celera | 10:85878258 | CCTGAGCTAATCCTC[C/T]AGCCCAGGGTGTGAT | 103136 |
rs30150032 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Pwp1 | Mm_Celera | 10:85878459 | TCTCTTACTAAAGTC[A/G]CTCTTTCCAATCTTT | 103136 |
rs30150524 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Pwp1 | Mm_Celera | 10:85875368 | CATGCTGTTCCTCAT[G/T]TGAAGGAGAGCACAC | 103136 |
rs30150526 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Pwp1 | Mm_Celera | 10:85875425 | TAGTTGATGTGTGCT[C/T]GGTGTTGATGCTTTG | 103136 |
rs30150528 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Pwp1 | Mm_Celera | 10:85875557 | GGCTGTTGGCGCTGT[A/G]GAGTCGGTGCTTTTC | 103136 |
rs30150530 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Pwp1 | Mm_Celera | 10:85875792 | GAACCATGGCTGCTG[C/T]CCTAGGTTCGCTCAG | 103136 |
rs30150532 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Pwp1 | Mm_Celera | 10:85875863 | TTTGTGAAACCTACG[A/C]TTGTAAGTGTGAGAG | 103136 |
rs30150654 | snp | G/T | 0.231111 | 0.249285 | downstream-variant-500B | Pwp1 | Mm_Celera | 10:85889465 | CCTGTATTTCAGACC[G/T]AGGACCTGGTTTTCC | 103136 |
rs30150656 | snp | C/T | 0.231111 | 0.249285 | downstream-variant-500B | Pwp1 | Mm_Celera | 10:85889525 | GTTGTCCTTACAGAG[C/T]TAGGATTACGGTGGG | 103136 |
rs30150658 | snp | C/G | 0.132653 | 0.220748 | downstream-variant-500B | Pwp1 | Mm_Celera | 10:85889535 | CAGAGCTAGGATTAC[C/G]GTGGGCTTTATGCCT | 103136 |
rs30150660 | snp | C/G | 0.152778 | 0.230321 | downstream-variant-500B | Pwp1 | Mm_Celera | 10:85889548 | ACGGTGGGCTTTATG[C/G]CTTCCCTGGTCTCAG | 103136 |
rs30150914 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Pwp1 | Mm_Celera | 10:85878684 | TGTCACTTAATCGAC[G/T]TTAGATAAGCCACTA | 103136 |
rs30150916 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Pwp1 | Mm_Celera | 10:85879007 | CCTGCAGACGTCCAC[A/G]GAGGACAGGGCAAGA | 103136 |
rs30150918 | snp | A/G | 0.32 | 0.24 | intron-variant | Pwp1 | Mm_Celera | 10:85879019 | CACGGAGGACAGGGC[A/G]AGAACCGTTGCTTCC | 103136 |
rs30150920 | snp | C/T | 0.32 | 0.24 | intron-variant | Pwp1 | Mm_Celera | 10:85879050 | CTGTGATAAGTTTCA[C/T]AGCTGAGGCCAGAGG | 103136 |
rs30150922 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Pwp1 | Mm_Celera | 10:85879130 | TGGGAACTGTTAGGC[C/T]TGCAGGATTCCAAGG | 103136 |
rs30151764 | snp | A/G | 0.32 | 0.24 | intron-variant | Pwp1 | Mm_Celera | 10:85879423 | TATTTAAAGGGACAA[A/G]CTGGGTTAAGTGACT | 103136 |
rs30151766 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Pwp1 | Mm_Celera | 10:85879639 | TGGTTTTGGACTTTA[C/T]GTTTCTGTTTACCTG | 103136 |
rs30151768 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Pwp1 | Mm_Celera | 10:85879930 | TGTGGTGTCTGCAGT[A/G]TTCTCGTTCATTCCT | 103136 |
rs30151770 | snp | C/G/T | 0.132653 | 0.220748 | intron-variant | Pwp1 | Mm_Celera | 10:85880717 | TGACCAGTATGTGTG[C/G/T]GAAGTGTGTTTTTCA | 103136 |
rs30151772 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Pwp1 | Mm_Celera | 10:85880725 | ATGTGTGCGAAGTGT[A/G]TTTTTCAAATTGAAT | 103136 |
rs30152814 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Pwp1 | Mm_Celera | 10:85880884 | TGTTACATCCAAGAT[G/T]CTCCCTAACCCAAGG | 103136 |
rs30152816 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Pwp1 | Mm_Celera | 10:85880912 | AGGTCATCAGGATGA[A/C]TGTTAAGGTACTGTT | 103136 |
rs30152818 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Pwp1 | Mm_Celera | 10:85880934 | GGTACTGTTCTGGGA[C/T]TTTATAGTGTTAGCT | 103136 |
rs30152820 | snp | A/G | 0.32 | 0.24 | intron-variant | Pwp1 | Mm_Celera | 10:85880995 | ATGTGTGGATGCTGA[A/G]ATGGAGGCCAAACTT | 103136 |
rs30152822 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Pwp1 | Mm_Celera | 10:85881030 | ACAAGGATATTCCAC[C/T]GTTTTGTTGTGAGCC | 103136 |
rs30153614 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Pwp1 | GRCm38.p3 | 10:85881071 | GGCGCTGGGTCCACC[A/G]AGCCACTTGTTCATT | 103136 |
rs30153616 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Pwp1 | Mm_Celera | 10:85881084 | CCAAGCCACTTGTTC[A/G]TTGAAAATGTCATCA | 103136 |
rs30153618 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Pwp1 | Mm_Celera | 10:85881429 | AGGAATTTGTTTGAG[C/T]ACAGGGTTTGAGACA | 103136 |
rs30153620 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Pwp1 | Mm_Celera | 10:85881740 | AGAGCCTGTGTGGCT[A/G]AGTCTGTAATCAGCT | 103136 |
rs30153622 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Pwp1 | Mm_Celera | 10:85881778 | CAACCTAGAAGTGCT[A/G]TTCGCATCTCAACAA | 103136 |
rs30154524 | snp | G/T | 0.32 | 0.24 | synonymous-codon | Pwp1 | Mm_Celera | 10:85882012 | TTTCAGAAATGTGCT[G/T]GCAAGTGCATCGGCA | 103136 |
rs30154526 | snp | A/C | 0.48 | 0.0979796 | intron-variant | Pwp1 | Mm_Celera | 10:85882154 | CAGATTACTGACTAA[A/C]GTAATCTGGACATTC | 103136 |
rs30154528 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Pwp1 | Mm_Celera | 10:85882412 | AGCTCTGCTCAGGGT[C/T]AGGTGTACTAGGAAC | 103136 |
rs30154530 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Pwp1 | Mm_Celera | 10:85882612 | CATAGTGGTATATAC[C/T]TTTAATTCCAGCTCT | 103136 |
rs30154532 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Pwp1 | Mm_Celera | 10:85882681 | GCTCTATGTAGCAAG[C/T]TTCAGACCAACCATG | 103136 |
rs30155484 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Pwp1 | Mm_Celera | 10:85882810 | CAGTTCTGTCTCACC[A/T]CACCGTAGCAGTATT | 103136 |
rs30155486 | snp | A/G | 0.124444 | 0.216185 | synonymous-codon | Pwp1 | Mm_Celera | 10:85882885 | GGTTCAGACTCTGCA[A/G]TTTCATCCATTTGAA | 103136 |
rs30155488 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Pwp1 | Mm_Celera | 10:85883086 | GTGCCATCTGATGCT[C/T]ACACGCTGTAGTACT | 103136 |
rs30155490 | snp | A/G | 0.32 | 0.24 | intron-variant | Pwp1 | Mm_Celera | 10:85883264 | TAAAAGCAACCCTGC[A/G]CTCAGTGACAGTCGC | 103136 |
rs30155492 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Pwp1 | Mm_Celera | 10:85883282 | CAGTGACAGTCGCCT[G/T]TTCCTTTTGAGATTC | 103136 |
rs30156474 | snp | A/G | 0.32 | 0.24 | intron-variant | Pwp1 | Mm_Celera | 10:85883318 | ATGGAGTCTGAGTTC[A/G]GTTGCTCAAAGTGGC | 103136 |
rs30156476 | snp | C/G | 0.32 | 0.24 | intron-variant | Pwp1 | Mm_Celera | 10:85883381 | CCAAAGGCAGATATT[C/G]CAAGGCCTGTGGAGA | 103136 |
rs30156478 | snp | C/G | 0.32 | 0.24 | intron-variant | Pwp1 | Mm_Celera | 10:85883542 | GAAGCTATGGGTATA[C/G]GAGAAATGAACAGCT | 103136 |