SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs3699900 | snp | A/G | 0.5 | 0 | intron-variant | Pard6g | Mm_Celera | 18:80065755 | TAATCTTGAAGGTGC[A/G]CTCTTTTTAAATAAC | 93737 |
rs6208063 | snp | A/G | 0.5 | 0 | intron-variant | Pard6g | GRCm38.p3 | 18:80083138 | GGGGTGAGAGTGGGG[A/G]GTAGATATCCACAGT | 93737 |
rs6208505 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Pard6g | GRCm38.p3 | 18:80083164 | ACAGTTGCACACAGT[A/G]CCGCTCACAACAGCC | 93737 |
rs6208559 | snp | C/T | 0.5 | 0 | intron-variant | Pard6g | GRCm38.p3 | 18:80083195 | CAAGCATGAACAAAG[C/T]TCAAGAATCCACCTG | 93737 |
rs6209100 | snp | C/T | 0.359862 | 0.224567 | intron-variant | Pard6g | Mm_Celera | 18:80083305 | GCTATCTATCACAAA[C/T]GGTGTGCTGAGGGAA | 93737 |
rs6209692 | snp | A/G | 0.484429 | 0.0868505 | intron-variant | Pard6g | GRCm38.p3 | 18:80083438 | TTAGAGCAGTTTTCT[A/G]GTCCCCAGAGAACAC | 93737 |
rs6210174 | snp | A/T | 0.359862 | 0.224567 | intron-variant | Pard6g | Mm_Celera | 18:80083515 | TCGCGCCGTCCTTGT[A/T]CCTGCCAGCATCTNT | 93737 |
rs6210209 | snp | A/G | 0.492188 | 0.0620098 | intron-variant | Pard6g | GRCm38.p3 | 18:80083529 | TNCCTGCCAGCATCT[A/G]TCTCTCACACCCTCT | 93737 |
rs29537608 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Pard6g | Mm_Celera | 18:80072723 | CAGAAAGTAGATTAG[C/T]TGATGATCTATATTA | 93737 |
rs29539018 | snp | C/T | 0.375 | 0.216506 | intron-variant | Pard6g | GRCm38.p3 | 18:80060524 | AGCCAGGTGTCCACA[C/T]CCCTTCGAGGTCCAG | 93737 |
rs29540647 | snp | G/T | 0.33241 | 0.236027 | intron-variant | Pard6g | GRCm38.p3 | 18:80058509 | ACAGGAAAGGACCAA[G/T]CACCACCCTGTCTGA | 93737 |
rs29545019 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Pard6g | GRCm38.p3 | 18:80071997 | GCTCCATGTTTGTGG[A/G]GCTTGTTTGGCTTCC | 93737 |
rs29546561 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Pard6g | GRCm38.p3 | 18:80086363 | GTCCTGCCCTGCCCT[A/G]GTGTGTACAGAGATA | 93737 |
rs29552950 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Pard6g | GRCm38.p3 | 18:80072041 | TTGAGCAATGGCCAG[A/G]CTCATCTCACATGTT | 93737 |
rs29555049 | snp | A/C | 0.375 | 0.216506 | intron-variant | Pard6g | GRCm38.p3 | 18:80085812 | AGTGAGAGAACAGAG[A/C]GGAGACCAGGAGGGA | 93737 |
rs29558490 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Pard6g | GRCm38.p3 | 18:80071949 | GCTTGGCCACTGGCA[C/G]GTTTCCCGGTTGGTT | 93737 |
rs29560176 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Pard6g | GRCm38.p3 | 18:80078891 | CTGTGAATGCAATGG[C/T]CGTGTATTGGCCATA | 93737 |
rs29561776 | snp | C/T | 0.5 | 0 | intron-variant | Pard6g | GRCm38.p3 | 18:80092759 | TGGTAGCTGCCACTG[C/T]AAACAGTTCTTGATG | 93737 |
rs29562518 | snp | G/T | 0.33241 | 0.236027 | intron-variant | Pard6g | GRCm38.p3 | 18:80065593 | TGTGTGCTGGCAAAT[G/T]CGAGACCCCAGTGTC | 93737 |
rs29562708 | snp | A/C | 0.375 | 0.216506 | intron-variant | Pard6g | GRCm38.p3 | 18:80049303 | TCCCGCTCTCCTCCC[A/C]CTCGGTAGCTGATGT | 93737 |
rs29574437 | snp | C/T | 0.415225 | 0.187619 | intron-variant | Pard6g | GRCm38.p3 | 18:80062720 | GTAGGTCGCTTGCTA[C/T]TGTTGTTTGGAGAAG | 93737 |
rs29576807 | snp | A/G | 0.375 | 0.216506 | intron-variant | Pard6g | GRCm38.p3 | 18:80066165 | TCTGGGTATAAGCCC[A/G]TACCCTACTTCCTTT | 93737 |
rs29576975 | snp | A/G | 0.5 | 0 | intron-variant | Pard6g | GRCm38.p3 | 18:80088232 | GAACGGATGGTTGAG[A/G]GAGGCCTCCTGAGAG | 93737 |
rs29578564 | snp | C/T | 0.455 | 0.143091 | utr-variant-3-prime, nc-transcript-variant | Pard6g | Mm_Celera | 18:80118480 | GGCGGTCACTGCTGT[C/T]GGCGGCTCCAGTGGA | 93737 |
rs29578678 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Pard6g | GRCm38.p3 | 18:80091478 | GGGCTCACCCTGGGT[A/G]GACTTTATGAAATTA | 93737 |
rs29580147 | snp | A/G | 0.5 | 0 | intron-variant | Pard6g | Mm_Celera | 18:80108460 | TGGGCTGGGGCGCAC[A/G]GCCCCGTATACCTCA | 93737 |
rs29588987 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Pard6g | GRCm38.p3 | 18:80066601 | CTGTCGTGAGGCAGC[A/G]GATAAAGGCAGGCGC | 93737 |
rs29621421 | snp | G/T | 0.32 | 0.24 | intron-variant | Pard6g | GRCm38.p3 | 18:80085040 | TTGTTTGGAAGTTTG[G/T]TTTTTTTAATTACCT | 93737 |
rs29621994 | snp | C/T | 0.484429 | 0.0868505 | intron-variant | Pard6g | GRCm38.p3 | 18:80064405 | CCATGTGTCAATAAT[C/T]GCCTTTTATCAAGTG | 93737 |
rs29627939 | snp | A/G | 0.375 | 0.216506 | intron-variant | Pard6g | GRCm38.p3 | 18:80060422 | CTAGTTCAAGACAGC[A/G]AGTCGGGCCTCTGTT | 93737 |
rs29629572 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Pard6g | GRCm38.p3 | 18:80077230 | AGGAGACCCAAGCAA[A/G]GACAGGAGAGAAAGT | 93737 |
rs29675988 | snp | G/T | 0.48 | 0.0979796 | upstream-variant-2KB | Pard6g | GRCm38.p3 | 18:80046181 | CACAATTCTGTAATG[G/T]ATATTACAATGTACA | 93737 |
rs29677102 | snp | A/G | 0.375 | 0.216506 | intron-variant | Pard6g | GRCm38.p3 | 18:80065397 | GGAGTGAGAGGGAAA[A/G]GCAGGTTCCACCCTG | 93737 |
rs29679321 | snp | C/T | 0.46875 | 0.121031 | intron-variant | Pard6g | GRCm38.p3 | 18:80064640 | CCCTACGAAGGAACG[C/T]TCTCAATGATTGGTT | 93737 |
rs29683131 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Pard6g | GRCm38.p3 | 18:80066614 | GCAGATAAAGGCAGG[A/C]GCACGTGGCAGAGTA | 93737 |
rs29715917 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Pard6g | GRCm38.p3 | 18:80091546 | TTTATAAAACTTGTG[C/G]TGTGGATGTATCATC | 93737 |
rs29719860 | snp | G/T | 0.375 | 0.216506 | intron-variant | Pard6g | GRCm38.p3 | 18:80060767 | GGCTTTCCTACACCT[G/T]CCTACTGTAGAGCCC | 93737 |
rs29721117 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Pard6g | Mm_Celera | 18:80115058 | GCTGCTTGGCAGATG[C/T]TGCCTCAGTGTGGTG | 93737 |
rs29725515 | snp | G/T | 0.493827 | 0.0552116 | intron-variant | Pard6g | Mm_Celera | 18:80073871 | TTACGATCAGAAAAA[G/T]CTACATAATTCCTTT | 93737 |
rs29765959 | snp | C/T | 0.5 | 0 | intron-variant | Pard6g | GRCm38.p3 | 18:80064571 | AAGTTGCTCACTTTA[C/T]GGCAGCTAGGAAGCA | 93737 |
rs29766463 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Pard6g | GRCm38.p3 | 18:80090524 | AGGAGAGAGAGCTGA[C/G]GAAGCCATCTGGAGC | 93737 |
rs29767281 | snp | A/G | 0.48 | 0.0979796 | upstream-variant-2KB | Pard6g | GRCm38.p3 | 18:80046261 | GTTGTTAAAGCCTGT[A/G]AGTTTCGTCCTAACT | 93737 |
rs29774302 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Pard6g | GRCm38.p3 | 18:80055405 | ATTTAGCAGTGAAAG[G/T]GATATTAGTATCCTG | 93737 |
rs29808987 | snp | C/T | 0.5 | 0 | intron-variant | Pard6g | GRCm38.p3 | 18:80091024 | TATATAACCTGGGTT[C/T]GCCTCAGCTCTCAGC | 93737 |
rs29813494 | snp | G/T | 0.375 | 0.216506 | intron-variant | Pard6g | GRCm38.p3 | 18:80070008 | CTTAAAAATTTATTT[G/T]AGGTTGATGAACTAT | 93737 |
rs29819783 | snp | C/G | 0.32 | 0.24 | intron-variant | Pard6g | GRCm38.p3 | 18:80061184 | GGGCTGAAGTGCGGG[C/G]CATAGGTTGGGAAGT | 93737 |
rs29820492 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Pard6g | GRCm38.p3 | 18:80092336 | TCAGAGACCACCCAG[A/G]AAAATACCCTTAGTT | 93737 |
rs29820503 | snp | C/T | 0.375 | 0.216506 | intron-variant | Pard6g | GRCm38.p3 | 18:80066163 | AGTCTGGGTATAAGC[C/T]CATACCCTACTTCCT | 93737 |
rs29824538 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Pard6g | GRCm38.p3 | 18:80071959 | TGGCACGTTTCCCGG[A/T]TGGTTCCTGTCCCCT | 93737 |
rs29826378 | snp | C/T | 0.32 | 0.24 | intron-variant | Pard6g | GRCm38.p3 | 18:80061755 | CCAAAGGACATCCCA[C/T]GACAGTGTCCTGGCC | 93737 |
rs29829322 | snp | C/T | 0.359862 | 0.224567 | intron-variant | Pard6g | GRCm38.p3 | 18:80086209 | TCACAGTGTTTCTCC[C/T]GGATACTTAGGGTTG | 93737 |
rs29831723 | snp | A/T | 0.5 | 0 | intron-variant | Pard6g | Mm_Celera | 18:80073220 | CCTTTAAAAAAAAAT[A/T]ATTGATTATGTCTCT | 93737 |
rs29859800 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Pard6g | GRCm38.p3 | 18:80091314 | CTGCCTCCCCTGTGG[A/G]AAAGTGGGTCAGCAC | 93737 |
rs29868104 | snp | C/T | 0.375 | 0.216506 | intron-variant | Pard6g | GRCm38.p3 | 18:80060802 | TGGCTACCTCAGCTC[C/T]GCCATCTTAGTCCTC | 93737 |
rs29874905 | snp | A/G | 0.359862 | 0.224567 | intron-variant | Pard6g | GRCm38.p3 | 18:80085098 | GGTGTTTCTTCGGGT[A/G]TGTGCTGGGCCCAGC | 93737 |
rs29875583 | snp | C/T | 0.387812 | 0.208586 | intron-variant | Pard6g | GRCm38.p3 | 18:80063542 | CAGAGAGTGACGGAT[C/T]AAGGGTAAGTCCTTC | 93737 |
rs29881907 | snp | A/G | 0.375 | 0.216506 | intron-variant | Pard6g | GRCm38.p3 | 18:80066437 | TGGTGTGCCTTTAGC[A/G]TTTTTATCATGGCCT | 93737 |
rs29913656 | snp | C/T | 0.359862 | 0.224567 | intron-variant | Pard6g | GRCm38.p3 | 18:80084982 | ATTCTCATCTTTAAA[C/T]GTGGGTCATCCTGCC | 93737 |
rs29919903 | snp | C/T | 0.375 | 0.216506 | intron-variant | Pard6g | Mm_Celera | 18:80070108 | ACATGTAGGATTTTT[C/T]CTTCTGAGCCAGGGT | 93737 |
rs29934230 | snp | A/G | 0.475309 | 0.108333 | intron-variant | Pard6g | GRCm38.p3 | 18:80085318 | GCTTATGGTTCATAC[A/G]GATTCAGGGTCCCCA | 93737 |
rs29935438 | snp | C/T | 0.48 | 0.0979796 | upstream-variant-2KB | Pard6g | GRCm38.p3 | 18:80046238 | AATGCATGAGACATT[C/T]TAAGATAGTTGTTAA | 93737 |
rs29951388 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Pard6g | Mm_Celera | 18:80065652 | CCCAAGCCTCCATGT[A/G]CAGCACCTGTCCAGC | 93737 |
rs29973503 | snp | G/T | 0.375 | 0.216506 | intron-variant | Pard6g | GRCm38.p3 | 18:80061088 | TGTGAGCTACACCCC[G/T]TCCCAGACGGGAGAA | 93737 |
rs30008737 | snp | A/G | 0.375 | 0.216506 | intron-variant | Pard6g | GRCm38.p3 | 18:80083064 | TCAAGATACACAAGG[A/G]CAGAATGATAAAATG | 93737 |
rs30019097 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Pard6g | GRCm38.p3 | 18:80079114 | AGGGAGCCTTCTCTG[A/G]TTGAGGCTTAGAGTA | 93737 |
rs30024521 | snp | C/T | 0.375 | 0.216506 | intron-variant | Pard6g | GRCm38.p3 | 18:80107219 | TCCAAAGATTTCCAC[C/T]TGGGTCCTTAAGATC | 93737 |
rs30030560 | snp | C/T | 0.415225 | 0.187619 | intron-variant | Pard6g | GRCm38.p3 | 18:80073421 | TTTCTTTGATAAGTG[C/T]ACTTCCGGTAAAGTG | 93737 |
rs30049731 | snp | A/G | 0.345679 | 0.230967 | intron-variant | Pard6g | GRCm38.p3 | 18:80106051 | CTGGGGACTGGGAAC[A/G]TGCAGCAGTGTGCAT | 93737 |
rs30060187 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Pard6g | Mm_Celera | 18:80084919 | CTGACTGTGTGTGAG[C/T]ACTTTGACTTTTTTT | 93737 |
rs30060975 | snp | G/T | 0.375 | 0.216506 | intron-variant | Pard6g | GRCm38.p3 | 18:80083067 | AGATACACAAGGACA[G/T]AATGATAAAATGAAA | 93737 |
rs30065496 | snp | G/T | 0.345679 | 0.230967 | intron-variant | Pard6g | Mm_Celera | 18:80073795 | CTTTTCAATGTAGAC[G/T]GTGAATTCTGAATGG | 93737 |
rs30069336 | snp | A/G | 0.375 | 0.216506 | intron-variant | Pard6g | GRCm38.p3 | 18:80060371 | AGTTATTCTTGTGTA[A/G]AAAGATGGGAGAGCT | 93737 |
rs30073878 | snp | C/T | 0.48 | 0.0979796 | upstream-variant-2KB | Pard6g | GRCm38.p3 | 18:80046332 | TTCTCCCCCCTCTTT[C/T]TAAGTGCTCTATCTA | 93737 |
rs30103795 | snp | G/T | 0.33241 | 0.236027 | intron-variant | Pard6g | Mm_Celera | 18:80058336 | TCTGTGAGCCAGGGT[G/T]CAGGCCTTCCCTCAG | 93737 |
rs30109173 | snp | C/T | 0.32 | 0.24 | intron-variant | Pard6g | Mm_Celera | 18:80065646 | GCAGAGCCCAAGCCT[C/T]CATGTACAGCACCTG | 93737 |
rs30111515 | snp | A/T | 0.475309 | 0.108333 | intron-variant | Pard6g | GRCm38.p3 | 18:80073744 | GCACGCTCACTGGCG[A/T]TCCTGCCTGTGTGCA | 93737 |
rs30112388 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Pard6g | GRCm38.p3 | 18:80061647 | ACCATGTTCTTGTAG[A/G]ACCCTGAAGCACAGC | 93737 |
rs30115391 | snp | G/T | 0.375 | 0.216506 | intron-variant | Pard6g | GRCm38.p3 | 18:80066322 | GTGACAGGGTCCTTC[G/T]TATAGCAACTCTGTT | 93737 |
rs30116911 | snp | A/C | 0.375 | 0.216506 | intron-variant | Pard6g | Mm_Celera | 18:80070130 | AGCCAGGGTTACCTT[A/C]TATAATATTTTCAGT | 93737 |
rs30118667 | snp | C/T | 0.5 | 0 | intron-variant | Pard6g | Mm_Celera | 18:80050827 | TCCATAGCACGCGCA[C/T]GCACATACACACACA | 93737 |
rs30149710 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Pard6g | GRCm38.p3 | 18:80077234 | GACCCAAGCAAAGAC[A/G]GGAGAGAAAGTCTCC | 93737 |
rs30159282 | snp | A/G | 0.375 | 0.216506 | intron-variant | Pard6g | GRCm38.p3 | 18:80085941 | GACACCCATGATCTT[A/G]TCCATCTCCAGCCCC | 93737 |
rs30170628 | snp | C/T | 0.487535 | 0.077957 | intron-variant | Pard6g | GRCm38.p3 | 18:80060663 | CTTAGATCCAGGTGG[C/T]TGAATCTAGGTAAAG | 93737 |
rs30171017 | snp | A/G | 0.5 | 0 | intron-variant | Pard6g | GRCm38.p3 | 18:80092800 | GTACCTGGCACACCC[A/G]TCCTTAAGACCGCAT | 93737 |
rs30171786 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Pard6g | GRCm38.p3 | 18:80079170 | TTTAGAAAGGAGCTC[A/G]CTGTGTTGTCAGTTT | 93737 |
rs30176007 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Pard6g | GRCm38.p3 | 18:80073728 | GCGCACATGCGCATG[C/T]GCACGCTCACTGGCG | 93737 |
rs30178427 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Pard6g | GRCm38.p3 | 18:80090523 | AAGGAGAGAGAGCTG[A/G]GGAAGCCATCTGGAG | 93737 |
rs30205617 | snp | G/T | 0.375 | 0.216506 | intron-variant | Pard6g | GRCm38.p3 | 18:80078948 | TCTTCCAGCAATTCC[G/T]TTCCTTCTGTCCTCT | 93737 |
rs30207723 | snp | C/T | 0.375 | 0.216506 | intron-variant | Pard6g | Mm_Celera | 18:80069902 | TTAAATAAGTTCTTA[C/T]AGTTTGTTTCTTCCT | 93737 |
rs30212206 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Pard6g | GRCm38.p3 | 18:80091469 | GTCGGGGGTGGGCTC[A/G]CCCTGGGTGGACTTT | 93737 |
rs30212352 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Pard6g | GRCm38.p3 | 18:80078835 | TGCCGAAGGACCCAC[A/T]CCAGTGCAGACCCAG | 93737 |
rs30215244 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Pard6g | GRCm38.p3 | 18:80106355 | GGGGTACAGCTGCTC[C/T]TCCCTATGGCTGTGG | 93737 |
rs30215575 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Pard6g | GRCm38.p3 | 18:80066553 | TTTCAGCTTGTGATT[C/T]TGGAAGTTCTGGTCC | 93737 |
rs30216738 | snp | C/T | 0.375 | 0.216506 | intron-variant | Pard6g | GRCm38.p3 | 18:80049306 | CGCTCTCCTCCCACT[C/T]GGTAGCTGATGTGTA | 93737 |
rs30220677 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Pard6g | GRCm38.p3 | 18:80087677 | AGCTGTAAATGTCAT[C/T]TTGTTTCGTTTCTTT | 93737 |
rs30246883 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Pard6g | GRCm38.p3 | 18:80091495 | ACTTTATGAAATTAT[A/G]AAGGATAGTAGTGAC | 93737 |
rs30257505 | snp | G/T | 0.408163 | 0.193609 | intron-variant | Pard6g | GRCm38.p3 | 18:80060812 | AGCTCTGCCATCTTA[G/T]TCCTCTGGTACTTTG | 93737 |
rs30258910 | snp | A/T | 0.5 | 0 | intron-variant | Pard6g | GRCm38.p3 | 18:80088361 | GGCTTTGTTATCCAA[A/T]GGTATCCAGCGGGGG | 93737 |
rs30260330 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Pard6g | GRCm38.p3 | 18:80101953 | GCCATCTGCCTCCTG[C/T]GAGCTGAGGAGGCCA | 93737 |
rs30261158 | snp | C/T | 0.48 | 0.0979796 | upstream-variant-2KB | Pard6g | Mm_Celera | 18:80046298 | CAAACTCCTAAGGAG[C/T]CAGGTTCCATCTTGG | 93737 |