SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs6276343 | snp | A/G | 0.5 | 0 | utr-variant-3-prime | Pcgf3 | Mm_Celera | 5:108502324 | TAGCTGGGCGCCACC[A/G]CCCCAACAGCCCTGC | 69587 |
rs29508997 | snp | C/T | 0.5 | 0 | intron-variant | Pcgf3 | Mm_Celera | 5:108475495 | ATGGAAGTGGAATTT[C/T]TGAGTTCAAGAGCCA | 69587 |
rs29526312 | snp | C/T | 0.375 | 0.216506 | intron-variant | Pcgf3 | Mm_Celera | 5:108486593 | ATGTAATAAATAAAT[C/T]TAAAAATAAATAAAT | 69587 |
rs29526566 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Pcgf3 | Mm_Celera | 5:108496437 | ATACACACACACACA[C/T]ATATATATATATGAA | 69587 |
rs33181429 | snp | A/G | 0.444444 | 0.157135 | downstream-variant-500B | Pcgf3 | GRCm38.p3 | 5:108503240 | TGTGTGTGTGTGTGT[A/G]CGTACTTTCTATCAA | 69587 |
rs33242529 | snp | A/T | 0.375 | 0.216506 | intron-variant | Pcgf3 | Mm_Celera | 5:108470548 | AAAAAAAAAAAAAAA[A/T]AATGTAAACAAGGTA | 69587 |
rs33367401 | snp | C/T | 0.5 | 0 | intron-variant | Pcgf3 | Mm_Celera | 5:108478783 | AGTACAATGATTTTG[C/T]TAATTTTGTATCCTA | 69587 |
rs33420585 | snp | A/C/T | 0.5 | 0 | upstream-variant-2KB | Pcgf3 | GRCm38.p3 | 5:108460316 | TATTCTGTTTTCCTT[A/C/T]CTTTCTTTCTTTCTT | 69587 |
rs33504238 | snp | C/T | 0.18 | 0.24 | utr-variant-3-prime | Pcgf3 | Mm_Celera | 5:108501305 | CATGGGGTTAACATG[C/T]GTTCTTTGGGTCTTT | 69587 |
rs33729197 | snp | A/G | 0.375 | 0.216506 | utr-variant-3-prime | Pcgf3 | Mm_Celera | 5:108501464 | TTTGTTAGGTTAGAG[A/G]ATGAATAAGACACTA | 69587 |
rs33743742 | snp | A/G | 0.498615 | 0.0262793 | intron-variant | Pcgf3 | Mm_Celera | 5:108476353 | GAGAGGAACACAGCA[A/G]TGGGCCAGGCATTAA | 69587 |
rs33753558 | snp | C/G | 0.444444 | 0.157135 | downstream-variant-500B | Pcgf3 | Mm_Celera | 5:108503220 | TGTGTGTGTGTTTGC[C/G]TTTGTGTGTGTGTGT | 69587 |
rs45632939 | snp | C/T | 0.124444 | 0.216185 | utr-variant-3-prime | Pcgf3 | Mm_Celera | 5:108501780 | ACTTCCTCTTTCACA[C/T]ACACAGTGTCAGAAG | 69587 |
rs45649625 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Pcgf3 | Mm_Celera | 5:108469135 | TCCAAGTAAGTCTCA[C/T]TGGGTCTTTAATTTA | 69587 |
rs45711625 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Pcgf3 | Mm_Celera | 5:108485989 | AGCATGGTCATTAAG[A/G]TTCCCATCCTGACTT | 69587 |
rs45774859 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Pcgf3 | Mm_Celera | 5:108484328 | GAGGCCACTTTGGGT[A/G]GCTTCCCTTTGTCAG | 69587 |
rs45779271 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Pcgf3 | Mm_Celera | 5:108488542 | CATACAGCCTAAGAC[A/G]GTCCTCTGAAAATGG | 69587 |
rs45816661 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Pcgf3 | Mm_Celera | 5:108471322 | CCACCTCCAGATTGT[A/G]TGTAATTAGTCCTTA | 69587 |
rs45855971 | snp | A/G | 0.132653 | 0.220748 | utr-variant-3-prime | Pcgf3 | Mm_Celera | 5:108501300 | TAGATCATGGGGTTA[A/G]CATGCGTTCTTTGGG | 69587 |
rs45874138 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Pcgf3 | Mm_Celera | 5:108476327 | GCCATGCAAACACAG[A/G]AGAGAACCGGGAGAG | 69587 |
rs46004903 | snp | C/T | 0.391111 | 0.206368 | synonymous-codon | Pcgf3 | Mm_Celera | 5:108473897 | ACAGTGACTGAGTGT[C/T]TGCACACATGTAAGT | 69587 |
rs46117950 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Pcgf3 | Mm_Celera | 5:108467252 | AGGAGCTATACCAGT[A/G]GTAACAATCGGCTAC | 69587 |
rs46165705 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Pcgf3 | Mm_Celera | 5:108494764 | GATGGATCCTTCCTT[C/G]TCTATCTGCACTCCT | 69587 |
rs46194180 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Pcgf3 | Mm_Celera | 5:108469863 | CTGATGGGCATCCCA[A/G]TCCCCTCCGTTTGAG | 69587 |
rs46194545 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Pcgf3 | Mm_Celera | 5:108474184 | GCTCTCAGATCTCAA[A/G]TCAAGTCGGTTTTTT | 69587 |
rs46219832 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Pcgf3 | Mm_Celera | 5:108498001 | TGAAGGTATAAGTGT[C/T]CATCTTGACTTGAAG | 69587 |
rs46244395 | snp | A/T | 0.132653 | 0.220748 | intron-variant | Pcgf3 | Mm_Celera | 5:108483898 | GTTATGGCAGAGCAA[A/T]GTTGCTTACATCATG | 69587 |
rs46282172 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Pcgf3 | Mm_Celera | 5:108468599 | TAGTGACAACCTCTT[C/T]GCCAGCCTGCCTGCC | 69587 |
rs46330690 | snp | A/T | 0.408163 | 0.193609 | intron-variant | Pcgf3 | Mm_Celera | 5:108499223 | ACATACAGACTTACT[A/T]CTTAGGGAGGACAGT | 69587 |
rs46393880 | snp | C/T | 0.444444 | 0.157135 | utr-variant-3-prime | Pcgf3 | Mm_Celera | 5:108500901 | GCTATGACTTAGCCG[C/T]GGTGTTTAATTTCTA | 69587 |
rs46450397 | snp | A/T | 0.132653 | 0.220748 | intron-variant | Pcgf3 | Mm_Celera | 5:108494439 | TGTATATGTTCCTGG[A/T]CTGTGCCCTCTGAAT | 69587 |
rs46460086 | snp | A/G | 0.32 | 0.24 | intron-variant | Pcgf3 | Mm_Celera | 5:108486028 | TTTCTGACTAGTAGC[A/G]TCCTTCAGACCCATC | 69587 |
rs46554526 | snp | A/C | 0.244898 | 0.249948 | intron-variant | Pcgf3 | Mm_Celera | 5:108487036 | TGGATTTGAGCGTAA[A/C]GTTAATTGGTGCTTT | 69587 |
rs46563409 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Pcgf3 | Mm_Celera | 5:108474032 | TCTTGAGTGGGGATC[A/G]GAAAGCTTTCCATAA | 69587 |
rs46571185 | snp | A/G | | | intron-variant | Pcgf3 | Mm_Celera | 5:108494219 | TGAGGATGTAGTTCA[A/G]TGGTAGAACGCTTGC | 69587 |
rs46579156 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Pcgf3 | Mm_Celera | 5:108471395 | TCTAAGCACCTTACT[A/G]AGCTCTTAGCCAGCA | 69587 |
rs46653237 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Pcgf3 | Mm_Celera | 5:108467393 | AAGACAGTTGGCAGC[C/T]TCTGAACGTTTGTAA | 69587 |
rs46661569 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Pcgf3 | Mm_Celera | 5:108477684 | CCTTTGTGTGGATAG[A/T]GGCAAGGAGGATTAG | 69587 |
rs46666797 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Pcgf3 | Mm_Celera | 5:108474889 | ATTCTCATGCTCTTG[C/T]CCCTTAGTGACTTAA | 69587 |
rs46680343 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Pcgf3 | Mm_Celera | 5:108476825 | GGTGAGCACCTGTAG[A/G]CGCTTTGGTATTATG | 69587 |
rs46735183 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Pcgf3 | Mm_Celera | 5:108473921 | TGTAAGTATGGCCAG[C/T]TCTACCGTGATCTGA | 69587 |
rs46759407 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Pcgf3 | Mm_Celera | 5:108483341 | GTACTAAAGACCACA[C/T]TTAAATGGCTCAGCT | 69587 |
rs46813430 | snp | A/G | 0.459184 | 0.136902 | intron-variant | Pcgf3 | Mm_Celera | 5:108471658 | CTAGGAGAGATAATG[A/G]CTTAGTCTGGGTGTG | 69587 |
rs46876232 | snp | A/G | 0.231111 | 0.249285 | utr-variant-3-prime | Pcgf3 | Mm_Celera | 5:108501854 | ATCCAAATTAACTCA[A/G]TCTTTAATGTCTGAC | 69587 |
rs46936202 | snp | A/G | 0.459184 | 0.136902 | intron-variant | Pcgf3 | Mm_Celera | 5:108484019 | GGCCCTGCCTTCTAC[A/G]CCTCCCAGGAATGTC | 69587 |
rs46971865 | snp | A/G | 0.459184 | 0.136902 | intron-variant | Pcgf3 | Mm_Celera | 5:108497791 | AGGAACCAGGGTTTT[A/G]GACTGTCAAGGGGCC | 69587 |
rs47088391 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Pcgf3 | Mm_Celera | 5:108475219 | CGGGTGAGTAAGAAC[A/G]TGGGCTGGAGCTCCC | 69587 |
rs47094669 | snp | C/T | 0.124444 | 0.216185 | utr-variant-3-prime | Pcgf3 | Mm_Celera | 5:108502207 | TAATCTCATGATATA[C/T]ATTTGTAACTTTGTA | 69587 |
rs47106687 | snp | C/G | 0.231111 | 0.249285 | downstream-variant-500B | Pcgf3 | Mm_Celera | 5:108503474 | AGGCTGGTGTGTTTC[C/G]TTTCTAAGGGCATAC | 69587 |
rs47112765 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Pcgf3 | Mm_Celera | 5:108483217 | GGGGTGAGTGACCCT[A/G]CTCTGGTCCCAAGGT | 69587 |
rs47117812 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Pcgf3 | Mm_Celera | 5:108468718 | GATGTGCAGTGTAAC[G/T]AGCAACAAAAGTAGG | 69587 |
rs47135959 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Pcgf3 | Mm_Celera | 5:108476107 | TCTTAGAGCTCTGTT[C/T]TGCTTTTTCTGTCCT | 69587 |
rs47170310 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Pcgf3 | Mm_Celera | 5:108476210 | CAGGTCCCCATTTGA[A/G]CTGCTGACGGGGTGG | 69587 |
rs47186754 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Pcgf3 | Mm_Celera | 5:108469774 | AAGGAGCCCTGCACA[G/T]CTGGAAGCACCCGTT | 69587 |
rs47186973 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Pcgf3 | Mm_Celera | 5:108474073 | TGTGGGTAACTTCTG[C/G]AGGGTGGTTTCTCCT | 69587 |
rs47342488 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Pcgf3 | Mm_Celera | 5:108477130 | TGCCTGGTACCCAAG[C/T]GTTGGGAGTTCTGGT | 69587 |
rs47359379 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Pcgf3 | Mm_Celera | 5:108499080 | ACCAGGATGTGTTCT[G/T]CGTGTTAAGAGAAAC | 69587 |
rs47421996 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Pcgf3 | Mm_Celera | 5:108476851 | TTATGTAAAGGGGTT[C/T]ATTGGCTTCAGTTTA | 69587 |
rs47517051 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Pcgf3 | Mm_Celera | 5:108498241 | TGAGAGCTGCTGTAG[C/T]GTGAGGACATCATGC | 69587 |
rs47620263 | snp | A/G | 0.124444 | 0.216185 | utr-variant-3-prime | Pcgf3 | Mm_Celera | 5:108502890 | AATTGTTTGGTTTCC[A/G]TGGTCCAGCTTTATT | 69587 |
rs47730914 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Pcgf3 | Mm_Celera | 5:108494498 | ATCTACTGGCATTCA[A/G]TGACAGAAAGGTCTT | 69587 |
rs47752980 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Pcgf3 | Mm_Celera | 5:108469439 | GATGTAGTTAATTAG[A/G]AAAAGGCATGAATAC | 69587 |
rs47760096 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Pcgf3 | Mm_Celera | 5:108487781 | TATATACTAGAACTT[C/T]TGAATTTTGGGTTAG | 69587 |
rs47785052 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Pcgf3 | Mm_Celera | 5:108470982 | TCCCTTCCTGATTTT[A/G]TACAAGGCTCCTGAG | 69587 |
rs47917618 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Pcgf3 | Mm_Celera | 5:108477731 | CATACAATATGTAGT[C/T]GGGCCTCATAGCCAA | 69587 |
rs47929679 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Pcgf3 | Mm_Celera | 5:108498400 | AGAAACACACTCTTA[A/C]GTGGTTGTGAGAACA | 69587 |
rs47939612 | snp | C/T | 0.124444 | 0.216185 | utr-variant-3-prime | Pcgf3 | Mm_Celera | 5:108502308 | ATTGCAACCGATGTC[C/T]TAGCTGGGCGCCACC | 69587 |
rs48119465 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Pcgf3 | Mm_Celera | 5:108483098 | GGGAATGGTAGAGCC[A/G]GAGCCAGTTGTGCTC | 69587 |
rs48119719 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Pcgf3 | Mm_Celera | 5:108485944 | GCACCAGTTCTTCCC[A/G]CCTTCTTGAATATGT | 69587 |
rs48124269 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Pcgf3 | Mm_Celera | 5:108485812 | GAGTTCCTCAAACTG[C/T]CTCCCTAGGATCTGT | 69587 |
rs48129849 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Pcgf3 | Mm_Celera | 5:108470135 | CTCCCTTTGCATAGT[A/G]GTTGATAAGGTGGCT | 69587 |
rs48233414 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Pcgf3 | Mm_Celera | 5:108483907 | GAGCAAAGTTGCTTA[C/T]ATCATGGTGGCCAGG | 69587 |
rs48293118 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Pcgf3 | Mm_Celera | 5:108475394 | TTTCTTAAACTGAAA[C/T]TTTGAAGTGAATGAG | 69587 |
rs48338485 | snp | A/T | 0.142012 | 0.225474 | intron-variant | Pcgf3 | Mm_Celera | 5:108484112 | GAGTTGGCAACCTTA[A/T]ACATGAGCCTTCAGA | 69587 |
rs48400726 | snp | C/T | 0.32 | 0.24 | intron-variant | Pcgf3 | Mm_Celera | 5:108484148 | TTTAACTCAGCCATA[C/T]ACTGGTGGGTTTTTG | 69587 |
rs48474845 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Pcgf3 | Mm_Celera | 5:108469583 | TGTCACTTAGTTTTA[A/T]AATATAAATAGCTTT | 69587 |
rs48477452 | snp | A/C | 0.408163 | 0.193609 | intron-variant | Pcgf3 | Mm_Celera | 5:108475376 | AAGTGGAATCTTATA[A/C]GTTTTCTTAAACTGA | 69587 |
rs48511061 | snp | C/G | 0.336735 | 0.234472 | intron-variant | Pcgf3 | Mm_Celera | 5:108486031 | CTGACTAGTAGCGTC[C/G]TTCAGACCCATCATC | 69587 |
rs48518724 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Pcgf3 | Mm_Celera | 5:108467905 | ATTTGTGTGGGCATG[C/T]TAAAGCACATGTGTG | 69587 |
rs48547876 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Pcgf3 | Mm_Celera | 5:108476890 | ATTTAGTGTGGAAGA[A/T]TGGGCAGCCAGGACT | 69587 |
rs48551957 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Pcgf3 | Mm_Celera | 5:108473922 | GTAAGTATGGCCAGT[C/T]CTACCGTGATCTGAA | 69587 |
rs48570054 | snp | A/T | 0.244898 | 0.249948 | intron-variant | Pcgf3 | Mm_Celera | 5:108486913 | AATGTCTAGGGCTCA[A/T]GTGGAAGAGAACAGA | 69587 |
rs48570547 | snp | A/C | | | intron-variant | Pcgf3 | Mm_Celera | 5:108468879 | CAAACAAACAAACAA[A/C]CAAAAACAAAAACAA | 69587 |
rs48620006 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Pcgf3 | Mm_Celera | 5:108483056 | ACACCTAATTCAGGT[C/T]GACTCAATTGGCAGA | 69587 |
rs48688186 | snp | A/C | 0.124444 | 0.216185 | utr-variant-3-prime | Pcgf3 | Mm_Celera | 5:108501124 | GACAGTTTTCCTTAG[A/C]GAGGCCATCACTGAA | 69587 |
rs48725390 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Pcgf3 | Mm_Celera | 5:108495280 | TTGTACCTGAATTTT[A/G]AGAAGCTTGAATGAA | 69587 |
rs48759816 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Pcgf3 | Mm_Celera | 5:108498920 | AGAACAGGATGGCCA[A/G]GGGTAAGAGATAGTA | 69587 |
rs48837833 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Pcgf3 | Mm_Celera | 5:108488687 | CCCCAGTCTGACTTC[A/G]GTCATCATGCAAAAG | 69587 |
rs48846225 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Pcgf3 | Mm_Celera | 5:108488351 | ATAGAACTTCCTAGT[A/G]TATTGTCTGAGTTGT | 69587 |
rs48964720 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Pcgf3 | Mm_Celera | 5:108476058 | CTTTCCCATACATCA[A/G]CTCTCTGTTGGGACT | 69587 |
rs49000574 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Pcgf3 | Mm_Celera | 5:108499465 | TGCTCTTTCTGTTAT[A/C]ATTTGTGCTTGCAGC | 69587 |
rs49025818 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Pcgf3 | Mm_Celera | 5:108497112 | ACAAGCGCCAGTATG[G/T]TGCGGCAGGTGCATG | 69587 |
rs49073999 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Pcgf3 | Mm_Celera | 5:108471013 | TGGGTTTATTAGTCA[A/G]TAAGCAAATGCAGTT | 69587 |
rs49080701 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Pcgf3 | Mm_Celera | 5:108483314 | AATATCTGCTGGACA[A/G]AGGAGACCCACGTAC | 69587 |
rs49181510 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Pcgf3 | Mm_Celera | 5:108498359 | CGGACCCAGAGGCTG[C/T]TTTTCTACTTATCAC | 69587 |
rs49205265 | snp | A/G/T | 0.124444 | 0.216185 | intron-variant | Pcgf3 | GRCm38.p3 | 5:108468388 | TGGAGGTTGTTGGGT[A/G/T]GACTCTACAAGCTAG | 69587 |
rs49272390 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Pcgf3 | Mm_Celera | 5:108476161 | CTGTGCCACCTGCTT[C/T]CATTCTGGCATGCAC | 69587 |
rs49300503 | snp | A/C | 0.124444 | 0.216185 | utr-variant-3-prime | Pcgf3 | Mm_Celera | 5:108502754 | ACCATTTTCACAAAA[A/C]TAGAAAACTCAGATA | 69587 |
rs49334015 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Pcgf3 | Mm_Celera | 5:108484658 | TCTTCTTGATTGAGC[C/T]CTTGCTTCCCTCCAC | 69587 |
rs49334776 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Pcgf3 | Mm_Celera | 5:108487934 | GAGCAGGTGAACACA[C/T]GTCCTCTGTGGATTT | 69587 |