SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs6369855 | snp | A/G | 0.5 | 0 | intron-variant | Parp11 | Mm_Celera | 6:127456124 | tatcatcgtggtagg[A/G]aacatgatagcatgc | 101187 |
rs6370343 | snp | A/G | 0.5 | 0 | intron-variant | Parp11 | Mm_Celera | 6:127456199 | gtagggagggaaaaa[A/G]ggagggagagagaca | 101187 |
rs6370377 | snp | A/G | 0.5 | 0 | intron-variant | Parp11 | Mm_Celera | 6:127456223 | agagacagagacaga[A/G]ggagaaagaccnaga | 101187 |
rs6370403 | snp | A/G | 0.5 | 0 | intron-variant | Parp11 | Mm_Celera | 6:127456235 | aganggagaaagacc[A/G]agagaccaactgatn | 101187 |
rs6370421 | snp | A/C | 0.5 | 0 | intron-variant | Parp11 | Mm_Celera | 6:127456250 | nagagaccaactgat[A/C]tggcttgggctttag | 101187 |
rs6371408 | snp | A/G | 0.5 | 0 | intron-variant | Parp11 | Mm_Celera | 6:127456410 | tacattctattctca[A/G]cccacataggctagt | 101187 |
rs29870013 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Parp11 | Mm_Celera | 6:127474754 | TATAACACCAGTCCA[C/T]GGTGACCAAAAACCT | 101187 |
rs29883082 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Parp11 | Mm_Celera | 6:127477267 | GTTTGCTAGTGAAAT[C/T]TCTCACCATCCTCTC | 101187 |
rs29921982 | snp | C/T | 0.5 | 0 | intron-variant | Parp11 | Mm_Celera | 6:127464964 | GTGTGTGTATAAACC[C/T]GGGTTTTTAGTCTTC | 101187 |
rs29961450 | snp | C/T | 0.456747 | 0.140554 | intron-variant | Parp11 | Mm_Celera | 6:127459336 | ACACTGACCAAGAGC[C/T]GACCAGATGAAGGTT | 101187 |
rs29976616 | snp | A/G | 0.5 | 0 | intron-variant | Parp11 | Mm_Celera | 6:127458014 | AGCAGACTTGGCAAC[A/G]GGCTTTAGAAACTTC | 101187 |
rs30010349 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Parp11 | Mm_Celera | 6:127456314 | CTCCAACAAGACCCC[A/G]ATCCTTTCAAACAGT | 101187 |
rs30019150 | snp | C/T | 0.5 | 0 | intron-variant | Parp11 | Mm_Celera | 6:127464695 | CTTCCCTCACACTGT[C/T]CTTGCTGAGTCAGCA | 101187 |
rs30019553 | snp | A/G | 0.456747 | 0.140554 | intron-variant | Parp11 | Mm_Celera | 6:127489704 | GATTGCAGGCATTAC[A/G]TACCATACCTAGCTC | 101187 |
rs30024815 | snp | C/G | 0.5 | 0 | intron-variant | Parp11 | Mm_Celera | 6:127462282 | ATTTTTCCCTGAAGA[C/G]TCTTTCTAGTGCTCT | 101187 |
rs30065620 | snp | C/T | 0.5 | 0 | intron-variant | Parp11 | Mm_Celera | 6:127463441 | AAGCCCTCACGTGCC[C/T]TTCTCAGCCTGGGCC | 101187 |
rs30071311 | snp | A/G | 0.5 | 0 | intron-variant | Parp11 | Mm_Celera | 6:127475053 | TATTCGAGCGAGCGT[A/G]TGAGTTGTAAGGAGT | 101187 |
rs30071313 | snp | A/C | 0.432133 | 0.171253 | intron-variant | Parp11 | Mm_Celera | 6:127459065 | GCAATTCACACTCCA[A/C]AACTAAATCTTCTGT | 101187 |
rs30122035 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Parp11 | Mm_Celera | 6:127474785 | GGGGCAGCACAGCCA[C/T]TGTGGGCAGCAGTGC | 101187 |
rs30124473 | snp | A/G/T | 0.5 | 0 | intron-variant | Parp11 | GRCm38.p3 | 6:127463867 | CTTTGTTCTTTGCTC[A/G/T]GGCCCGATCCTGACA | 101187 |
rs30167596 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Parp11 | Mm_Celera | 6:127458460 | AGCCCTGGGTCAGGA[A/T]CATCAAAACAACAGC | 101187 |
rs30167622 | snp | C/T | 0.5 | 0 | intron-variant | Parp11 | Mm_Celera | 6:127464431 | GTGTGTTAGTGTAGT[C/T]CTGGGTATTCAGTGA | 101187 |
rs30169826 | snp | A/G | 0.345679 | 0.230967 | utr-variant-3-prime, intron-variant | Parp11 | Mm_Celera | 6:127491938 | CCGGTTTTGTTAAAG[A/G]CCGATGCTGTTGCCA | 101187 |
rs30209969 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Parp11 | Mm_Celera | 6:127454372 | TTCGTTCATTCATTC[A/G]TTCGTTCATTCAAAC | 101187 |
rs30219639 | snp | A/G | 0.493827 | 0.0552116 | intron-variant | Parp11 | Mm_Celera | 6:127500783 | TGGCTGGTCTGAGGA[A/G]CTGAGATTGGAGTTA | 101187 |
rs30219641 | snp | A/G | 0.456747 | 0.140554 | intron-variant | Parp11 | Mm_Celera | 6:127488280 | CGCATCTTTGGCACT[A/G]GAATGGATTGAAGCT | 101187 |
rs30224086 | snp | G/T | 0.5 | 0 | intron-variant | Parp11 | Mm_Celera | 6:127462144 | ATTTTTCCCCCCTAC[G/T]GAGTATTTTACTAAA | 101187 |
rs30266598 | snp | A/G | 0.5 | 0 | intron-variant | Parp11 | Mm_Celera | 6:127462259 | ACAGCTTGAGATGCC[A/G]TGGGAAGATTTTTCC | 101187 |
rs30315256 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Parp11 | Mm_Celera | 6:127453955 | TCGTGGCTGTCCCGC[G/T]TCGCGGGGGCCTCCT | 101187 |
rs30316611 | snp | C/T | 0.375 | 0.216506 | intron-variant | Parp11 | Mm_Celera | 6:127490938 | TCTTCAGTTAACTCC[C/T]GGTTCTAGAATTACT | 101187 |
rs30317476 | snp | C/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | Parp11 | Mm_Celera | 6:127472576 | TGAGCTGTGTCTTTC[C/T]AACGATGGTGGTGCT | 101187 |
rs30360860 | snp | A/G | 0.290657 | 0.246672 | downstream-variant-500B, intron-variant | Parp11 | Mm_Celera | 6:127494561 | CTGGCACTCCCAGCA[A/G]TCTAAGATCAGCTTT | 101187 |
rs30409694 | snp | A/G | 0.5 | 0 | intron-variant | Parp11 | Mm_Celera | 6:127476452 | CATTGAGTGTTGATT[A/G]AGTGCCAGCCATGTG | 101187 |
rs30414400 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Parp11 | Mm_Celera | 6:127474745 | CCTCTTGTATATAAC[A/G]CCAGTCCACGGTGAC | 101187 |
rs30415092 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Parp11 | Mm_Celera | 6:127490983 | ATGTGTAGCCAGCAG[C/T]TTCTTGGGTAGAGGA | 101187 |
rs30428767 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Parp11 | Mm_Celera | 6:127475410 | AGACTATACAAACTG[A/C]ACAACAGAGACAGAA | 101187 |
rs30466223 | snp | A/G | 0.5 | 0 | intron-variant | Parp11 | Mm_Celera | 6:127479906 | TGGGCCCAACTCTCC[A/G]GGCCTCAGTTTGTTT | 101187 |
rs30503016 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Parp11 | Mm_Celera | 6:127462666 | TTAAAATGGAGTATT[G/T]GGTCCTTGAGGTTGT | 101187 |
rs30515327 | snp | A/T | 0.5 | 0 | intron-variant | Parp11 | Mm_Celera | 6:127463865 | GGCTTTGTTCTTTGC[A/T]CGGGCCCGATCCTGA | 101187 |
rs30525265 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Parp11 | Mm_Celera | 6:127464159 | CTACTGTTGCACTAA[C/T]GTCTTTTCTTTAACT | 101187 |
rs30608044 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Parp11 | Mm_Celera | 6:127462733 | AGTGAAAGAGAACTC[A/G]CTGTATGCAAGAGAG | 101187 |
rs30667874 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Parp11 | Mm_Celera | 6:127462405 | AGTGCCAGGAAAGAG[C/T]GAAAACTGGGCTAGG | 101187 |
rs30699444 | snp | C/T | 0.475309 | 0.108333 | intron-variant | Parp11 | Mm_Celera | 6:127497189 | AACACAGATTTTACG[C/T]CAAAGACATTAATAT | 101187 |
rs30701928 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Parp11 | Mm_Celera | 6:127486147 | GTCTGTTAGCTTATG[A/T]CTTTTTATAGGTGAG | 101187 |
rs30764906 | snp | C/G | 0.5 | 0 | intron-variant | Parp11 | Mm_Celera | 6:127463652 | ATTGTCGTTGTATCT[C/G]CGTGCCACTCCAGAG | 101187 |
rs30768816 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Parp11 | Mm_Celera | 6:127489518 | TCATTTGACCACCGA[A/G]CTCCATACCCACTCT | 101187 |
rs30810960 | snp | A/T | 0.49827 | 0.0293608 | intron-variant | Parp11 | Mm_Celera | 6:127458300 | TGTCCTGAATGGTGT[A/T]GCTTGATCTCCCAGT | 101187 |
rs30842126 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Parp11 | Mm_Celera | 6:127464092 | TCAGAGAGTAGAATG[A/G]TAGACAAGGGAGAGG | 101187 |
rs30901620 | snp | C/G | 0.5 | 0 | intron-variant | Parp11 | Mm_Celera | 6:127484621 | GATTTCTCCCATTTC[C/G]TTGTGTGATATGGGC | 101187 |
rs30906092 | snp | A/T | 0.5 | 0 | intron-variant | Parp11 | Mm_Celera | 6:127463517 | TACCTGCCGGGTGTC[A/T]GCAGCTGTGCTGGCC | 101187 |
rs30907139 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Parp11 | Mm_Celera | 6:127477290 | ATCCTCTCTCTCTGT[C/T]TGTGTCCTGTGGCAT | 101187 |
rs30914361 | snp | A/G | 0.5 | 0 | intron-variant | Parp11 | Mm_Celera | 6:127459811 | AGTGATGGACTGTAA[A/G]CTGTGAGGTGAGCAA | 101187 |
rs30952419 | snp | C/T | 0.475309 | 0.108333 | upstream-variant-2KB, utr-variant-5-prime, intron-variant | Parp11 | Mm_Celera | 6:127453495 | GGTGGGTATGATGGC[C/T]GGCTTCAAACAGCTT | 101187 |
rs30954731 | snp | A/T | 0.5 | 0 | intron-variant | Parp11 | Mm_Celera | 6:127464457 | AGTGAAAGTAACTAA[A/T]TGGTTTATTTTGAGA | 101187 |
rs30991518 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Parp11 | Mm_Celera | 6:127451138 | GGACACTGCACACAC[A/T]TTATACATAGAAGGT | 101187 |
rs31000849 | snp | A/G | 0.5 | 0 | intron-variant | Parp11 | Mm_Celera | 6:127463518 | ACCTGCCGGGTGTCA[A/G]CAGCTGTGCTGGCCG | 101187 |
rs33893533 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Parp11 | Mm_Celera | 6:127480405 | GCCATTTCTACAGCA[C/T]CTGTTATATCTTCTT | 101187 |
rs33893893 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Parp11 | Mm_Celera | 6:127512470 | GATGAGGTTTTTGTT[C/T]TCATTTTGGCAGGTA | 101187 |
rs45632298 | snp | C/T | 0.231111 | 0.249285 | upstream-variant-2KB, downstream-variant-500B | Parp11, Gm34148 | Mm_Celera | 6:127446652 | GCAAGACGTGTACAA[C/T]GTCCTTTTCCAAACA | 101187 |
rs45647948 | snp | A/G | 0.42 | 0.183303 | intron-variant | Parp11 | Mm_Celera | 6:127508503 | TATGCTCCAGTGTAT[A/G]ATTTCAACCAAGATC | 101187 |
rs45650959 | snp | A/G | 0.35503 | 0.226867 | upstream-variant-2KB | Parp11 | Mm_Celera | 6:127445799 | TCATAGAAACATAAA[A/G]TGTTGGCAAGGCTGT | 101187 |
rs45707740 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Parp11 | Mm_Celera | 6:127484364 | AATCGGCTCTTGGAA[A/G]CTCTTTGCTAAGAGA | 101187 |
rs45735174 | snp | C/G | | | intron-variant | Parp11 | Mm_Celera | 6:127486829 | ATCCAGGAAATTCAG[C/G]ACAATGAAAAGATCA | 101187 |
rs45735586 | snp | A/G | 0.124444 | 0.216185 | utr-variant-3-prime, intron-variant | Parp11 | Mm_Celera | 6:127492350 | ATCTCCCACAGTTGA[A/G]CTGAGCACTGCTGCT | 101187 |
rs45751095 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Parp11 | Mm_Celera | 6:127497015 | GTCTCCTGCTGTAAG[G/T]TTGCACAATCCCTTC | 101187 |
rs45806519 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Parp11 | Mm_Celera | 6:127503157 | CCTGATTGGCACATA[C/T]GGCCTTCACTTAAAG | 101187 |
rs45880200 | snp | G/T | 0.244898 | 0.249948 | intron-variant | Parp11 | Mm_Celera | 6:127458958 | GCAGGGAGAAGACTT[G/T]GTGGGTGATAGAGAT | 101187 |
rs45954201 | snp | C/G | 0.132653 | 0.220748 | upstream-variant-2KB, intron-variant | Parp11 | Mm_Celera | 6:127451928 | ATCAGGATGATGCTA[C/G]CTAGCCTTGAGAAGG | 101187 |
rs45961449 | snp | C/T | 0.32 | 0.24 | intron-variant | Parp11 | Mm_Celera | 6:127496968 | AGGGTTTCCTAACAC[C/T]GAACAGCAGCCTCTC | 101187 |
rs45969748 | snp | A/C | | | intron-variant | Parp11 | Mm_Celera | 6:127510812 | TCGCTATCCTGGACC[A/C]TTCTGGTTCCCTCAG | 101187 |
rs45974889 | snp | A/G | 0.32 | 0.24 | intron-variant | Parp11 | Mm_Celera | 6:127512001 | TGAGAATTCTGGGAA[A/G]TAGTAAGAGATAAAA | 101187 |
rs45986973 | snp | C/G | 0.124444 | 0.216185 | upstream-variant-2KB | Parp11 | Mm_Celera | 6:127445229 | ACATCAGGCTTAACT[C/G]CTGTATTTTGGTTTT | 101187 |
rs46030593 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Parp11 | Mm_Celera | 6:127510298 | TTGATATGTCAGACT[C/T]AGAGGGGCCAAAGGC | 101187 |
rs46032753 | snp | G/T | | | intron-variant | Parp11 | Mm_Celera | 6:127487381 | CAGACCACCTGTGGG[G/T]CCTTCCAACTGGGGG | 101187 |
rs46126452 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Parp11 | Mm_Celera | 6:127500667 | TCAGCCTTCCTAGTA[A/G]CCACCGCAAAGGGGC | 101187 |
rs46133463 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Parp11 | Mm_Celera | 6:127500512 | CTGCACCTACATCAG[C/T]CCTCCAACAGCCAGG | 101187 |
rs46135994 | snp | A/G | 0.124444 | 0.216185 | intron-variant, upstream-variant-2KB | Parp11, Gm34148 | Mm_Celera | 6:127449363 | CCTAGGGGACAAGCT[A/G]GCCCACGGATCTGGA | 101187 |
rs46179233 | snp | A/T | 0.132653 | 0.220748 | utr-variant-3-prime, intron-variant | Parp11 | Mm_Celera | 6:127493179 | CTCGGGAAATTATGC[A/T]CAGTGCTTTGGCACA | 101187 |
rs46188722 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Parp11 | Mm_Celera | 6:127510260 | GCAGACTATAGAACT[C/T]ATGGTCTGATTCTAT | 101187 |
rs46206470 | snp | G/T | 0.197531 | 0.244432 | intron-variant | Parp11 | Mm_Celera | 6:127504239 | GAGAGTAGATAGCAG[G/T]CAGGCAAGGTCACAG | 101187 |
rs46258785 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Parp11 | Mm_Celera | 6:127501399 | CTGAGTTAAAGTGGA[C/T]TCCTTCCTGGATCTG | 101187 |
rs46323604 | snp | A/G | | | intron-variant | Parp11 | Mm_Celera | 6:127458915 | GAGCCTAATAGTCTC[A/G]GTGTAGGAAGGGTGG | 101187 |
rs46364445 | snp | A/C | 0.132653 | 0.220748 | upstream-variant-2KB, intron-variant | Parp11 | Mm_Celera | 6:127452642 | AACCATTTGGCAACA[A/C]TTTTTAGAATTTCTT | 101187 |
rs46369177 | snp | A/G | | | intron-variant | Parp11 | Mm_Celera | 6:127485428 | GCCTCGAACTCAGAA[A/G]TCTACCTGCCTCTGC | 101187 |
rs46376507 | snp | A/C | 0.231111 | 0.249285 | utr-variant-3-prime, intron-variant | Parp11 | Mm_Celera | 6:127492441 | ATTTCCTTTGTTTTC[A/C]AAGCCCTGCAGAGGC | 101187 |
rs46379768 | snp | A/C | | | intron-variant | Parp11 | Mm_Celera | 6:127510726 | TGAATATAGAAAACA[A/C]AAAGCATGGTTGGTG | 101187 |
rs46381476 | snp | A/C | 0.32 | 0.24 | intron-variant | Parp11 | Mm_Celera | 6:127506325 | ACACCAAGCTTTTTG[A/C]TTTTGAAACTGTCCT | 101187 |
rs46394011 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Parp11 | Mm_Celera | 6:127490263 | CACAAGGTGGAAGAG[A/C]GATGTGCACGTCTGC | 101187 |
rs46415853 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Parp11 | Mm_Celera | 6:127500380 | GCAGCATGGCAGTGG[C/T]GTGTGCAGTGCTAAC | 101187 |
rs46424444 | snp | A/G | | | intron-variant, upstream-variant-2KB | Parp11 | Mm_Celera | 6:127474222 | TAATCGGATGTGTCT[A/G]TCTTTGTCTTCAGAA | 101187 |
rs46437783 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Parp11 | Mm_Celera | 6:127497467 | GAAGCCGCAAACATA[A/G]TAAGCCTGTACTTGA | 101187 |
rs46456039 | snp | A/G | 0.231111 | 0.249285 | upstream-variant-2KB | Parp11 | Mm_Celera | 6:127445924 | TGAAAGAGTTTAAAC[A/G]GATTGAATTGTGGTG | 101187 |
rs46508673 | snp | A/G | | | intron-variant | Parp11 | Mm_Celera | 6:127463121 | GAGTCCTAGAAAATC[A/G]TTGACCCTAAAACAG | 101187 |
rs46530022 | snp | G/T | | | intron-variant | Parp11 | Mm_Celera | 6:127479155 | CATCATAAGCACCAT[G/T]GTACTTGTGATCTTG | 101187 |
rs46567180 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Parp11 | Mm_Celera | 6:127450782 | TTCAATCAGAGCCTA[C/T]GTGTTCATCAGTGCA | 101187 |
rs46576515 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Parp11 | Mm_Celera | 6:127488597 | CAGCCCTTCACATGT[C/T]GTCTTCATCCCACAT | 101187 |
rs46577552 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Parp11 | Mm_Celera | 6:127508510 | CAGTGTATGATTTCA[A/G]CCAAGATCTGTAACC | 101187 |
rs46618538 | snp | C/G/T | 0.408163 | 0.193609 | intron-variant | Parp11 | Mm_Celera | 6:127502447 | ATTAAAGAAGGCATC[C/G/T]TGGGACGCTTTCTTG | 101187 |
rs46618989 | snp | A/C | 0.32 | 0.24 | intron-variant | Parp11 | Mm_Celera | 6:127502742 | CAAAAGTCCATTTTC[A/C]TACTTAAATTTTAGG | 101187 |
rs46649646 | snp | C/T | 0.231111 | 0.249285 | upstream-variant-2KB | Parp11 | Mm_Celera | 6:127445896 | GCTTCTCCGAGTGGG[C/T]AGTTTTCATGTCTGA | 101187 |