SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs8239772 | snp | A/G | 0.18 | 0.24 | intron-variant | Gnb5 | GRCm38.p3 | 9:75327797 | TGAGACCTTAGTTAA[A/G]AAGAAACGACCACAA | 14697 |
rs8239773 | snp | A/G | 0.18 | 0.24 | intron-variant | Gnb5 | GRCm38.p3 | 9:75327780 | AGAAACGACCACAAC[A/G]AAACCAGACAAAAAC | 14697 |
rs8239774 | snp | C/T | 0.18 | 0.24 | intron-variant | Gnb5 | GRCm38.p3 | 9:75327765 | AAAACCAGACAAAAA[C/T]TAAAAAGCAAAAATA | 14697 |
rs8239775 | in-del | -/TA | 0.5 | 0 | intron-variant | Gnb5 | GRCm38.p3 | 9:75327709 | ATATTAAAAGAAAAA[-/TA]NAAAAGCCATTNNTG | 14697 |
rs8239776 | in-del | -/A | 0.493827 | 0.0552116 | intron-variant | Gnb5 | Mm_Celera | 9:75327710 | TATTAAAAGAAAAAN[-/A]AAAAGCCATTNNTGG | 14697 |
rs8239777 | snp | A/C | 0.18 | 0.24 | intron-variant | Gnb5 | GRCm38.p3 | 9:75327699 | AAAAAAAAAGCCATT[A/C]ATGGAATTTCAATCA | 14697 |
rs8239778 | snp | A/G | 0.475309 | 0.108333 | intron-variant | Gnb5 | GRCm38.p3 | 9:75327698 | AAAAAAAAGCCATTC[A/G]TGGAATTTCAATCAT | 14697 |
rs8239779 | snp | A/G | 0.21875 | 0.248039 | intron-variant | Gnb5 | GRCm38.p3 | 9:75327679 | AATTTCAATCATTAC[A/G]CCCTGCTGGAGGTAG | 14697 |
rs8239780 | snp | C/T | 0.226843 | 0.248925 | intron-variant | Gnb5 | GRCm38.p3 | 9:75327675 | TCAATCATTACGCCC[C/T]GCTGGAGGTAGGGAA | 14697 |
rs8239781 | in-del | -/G | 0.644636 | 0.0747315 | intron-variant | Gnb5 | Mm_Celera | 9:75327629 | TCCTTCACAAATNNN[-/G]CCTTGTAANNNNAGA | 14697 |
rs8254952 | snp | A/G | 0.345679 | 0.230967 | intron-variant | Gnb5 | Mm_Celera | 9:75327341 | TCAGGCGGCGAAGGA[A/G]GAAAGAGCCGTCCTG | 14697 |
rs8254953 | snp | A/G | 0.453686 | 0.144955 | intron-variant | Gnb5 | Mm_Celera | 9:75327436 | ATTCTCCTGCAATGT[A/G]GAAGTATATGGCAGT | 14697 |
rs8254954 | snp | C/T | 0.491493 | 0.0646602 | intron-variant | Gnb5 | Mm_Celera | 9:75327448 | TGTGGAAGTATATGG[C/T]AGTGTTTGCGCCCTT | 14697 |
rs8254955 | snp | A/T | 0.486111 | 0.0821678 | intron-variant | Gnb5 | Mm_Celera | 9:75327455 | GTATATGGCAGTGTT[A/T]GCGCCCTTGTCTGAC | 14697 |
rs8254956 | snp | A/G | 0.15879 | 0.232768 | intron-variant | Gnb5 | Mm_Celera | 9:75327458 | TATGGCAGTGTTTGC[A/G]CCCTTGTCTGACACG | 14697 |
rs8254957 | snp | C/T | 0.15879 | 0.232768 | intron-variant | Gnb5 | Mm_Celera | 9:75327472 | CGCCCTTGTCTGACA[C/T]GCACTGTGCCTTGGG | 14697 |
rs8254958 | snp | A/C | 0.496528 | 0.0415217 | intron-variant | Gnb5 | Mm_Celera | 9:75327489 | CACTGTGCCTTGGGG[A/C]TGACCCCAGCACTGG | 14697 |
rs8259460 | snp | A/C | 0.497041 | 0.0383476 | intron-variant | Gnb5 | Mm_Celera | 9:75327536 | CACCCTGGAGAATGT[A/C]ACTGATCTCGAATTA | 14697 |
rs8259461 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Gnb5 | GRCm38.p3 | 9:75327585 | TGGATTGTGTCTGAC[C/T]NCCTTTGATGANNNN | 14697 |
rs8259462 | in-del | -/C | 0.345679 | 0.230967 | intron-variant | Gnb5 | GRCm38.p3 | 9:75327586 | GGATTGTGTCTGACN[-/C]CCTTTGATGANNNNN | 14697 |
rs8259473 | in-del | -/C | 0.64 | 0.08 | intron-variant | Gnb5 | Mm_Celera | 9:75327630 | CTNNNNTTACAAGGN[-/C]NNATTTGTGAAGGAA | 14697 |
rs8260621 | snp | A/T | 0.48 | 0.0979796 | intron-variant | Gnb5 | Mm_Celera | 9:75328050 | ACCTCAATTTTGGAG[A/T]AATGTGTTATGCAGC | 14697 |
rs8260622 | snp | A/G | 0.165289 | 0.235211 | intron-variant | Gnb5 | GRCm38.p3 | 9:75328046 | CAATTTTGGAGTAAT[A/G]TGTTATGCAGCAATA | 14697 |
rs8260623 | snp | G/T | 0.152778 | 0.230321 | intron-variant | Gnb5 | GRCm38.p3 | 9:75328044 | ATTTTGGAGTAATGT[G/T]TTATGCAGCAATACA | 14697 |
rs8260624 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Gnb5 | Mm_Celera | 9:75327992 | AGATTAGCTGCATAG[A/G]CTATGCCAGAAGTTG | 14697 |
rs8260625 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Gnb5 | GRCm38.p3 | 9:75327980 | TAGACTATGCCAGAA[A/G]TTGTATATTCTAAAC | 14697 |
rs8260626 | in-del | -/G | 0.396694 | 0.202437 | intron-variant | Gnb5 | GRCm38.p3 | 9:75327954 | TAAACAGAGTTAAAT[-/G]TCTTCTTATTAAACA | 14697 |
rs29639498 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Gnb5 | Mm_Celera | 9:75307639 | TTTTGCCCACTTTTT[A/T]AAAAATTCATTGAGC | 14697 |
rs29640306 | snp | A/G | 0.375 | 0.216506 | intron-variant | Gnb5 | Mm_Celera | 9:75317054 | ACCTGAACCACCGAC[A/G]TGTTTGGTTTTTTTA | 14697 |
rs29687657 | snp | A/T | 0.5 | 0 | intron-variant | Gnb5 | Mm_Celera | 9:75316842 | ACCTTGTTTTTTTTT[A/T]AAATAGGTCTCTCAT | 14697 |
rs29695786 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Gnb5 | Mm_Celera | 9:75307500 | AGTTTTAGGAATTCT[C/T]GGGTATAGCTAATTG | 14697 |
rs29737091 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Gnb5 | Mm_Celera | 9:75337792 | TACACCTATATACCA[C/T]GGGGAGACAGAACAG | 14697 |
rs29738216 | snp | C/G | 0.5 | 0 | intron-variant | Gnb5 | Mm_Celera | 9:75323193 | ATAGATAGATAGATA[C/G]ATAGATAGATAGATA | 14697 |
rs29738846 | snp | A/C | 0.475309 | 0.108333 | utr-variant-3-prime, upstream-variant-2KB, intron-variant, nc-transcript-variant | Myo5c, Gnb5 | Mm_Celera | 9:75305259 | CCCTAGCAACCTGAC[A/C]ACCCTCCAGTCTGAT | 14697 |
rs29782302 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Gnb5 | Mm_Celera | 9:75317377 | AAGGTTATCCTCCAC[A/G]ACATAATGAGTTTGA | 14697 |
rs29879056 | snp | C/T | 0.432133 | 0.171253 | intron-variant, downstream-variant-500B | Gnb5, Myo5c | Mm_Celera | 9:75306529 | TCTCTACAACCTTTG[C/T]GACTTTATCTCAAAA | 14697 |
rs29887775 | snp | A/G | 0.5 | 0 | intron-variant | Gnb5 | Mm_Celera | 9:75330556 | CTGCCGAGAAGAGAT[A/G]CTGTGACCACAGCAA | 14697 |
rs29892234 | snp | A/C | 0.5 | 0 | intron-variant | Gnb5 | Mm_Celera | 9:75325798 | ACCATCAGCGCAGTG[A/C]CTGGGCTGTTAGTGT | 14697 |
rs30034372 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Gnb5 | Mm_Celera | 9:75330851 | GACCAAGCATTCACA[C/T]CCATGAGTCTATGGG | 14697 |
rs30037086 | snp | C/T | 0.444444 | 0.157135 | intron-variant, upstream-variant-2KB | Gnb5, LOC102636700 | Mm_Celera | 9:75312814 | AACATGACTTCTGGG[C/T]CAGCCTGCTCTACAA | 14697 |
rs30038864 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Gnb5 | Mm_Celera | 9:75320844 | TCACCGGGCAGTGGT[A/G]GCGCACGCCTTTAAT | 14697 |
rs30137837 | snp | C/T | 0.5 | 0 | intron-variant | Gnb5 | Mm_Celera | 9:75323049 | CACATGGCAGCTCAC[C/T]GGTCTGTAACTCCAG | 14697 |
rs30174053 | snp | C/G | 0.5 | 0 | intron-variant | Gnb5 | Mm_Celera | 9:75323189 | ATAGATAGATAGATA[C/G]ATAGATAGATAGATA | 14697 |
rs30183085 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Gnb5 | Mm_Celera | 9:75330949 | CCTTTTCCCTTTAAC[A/G]AAAGAGATTACTCAC | 14697 |
rs30183473 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Gnb5 | Mm_Celera | 9:75320850 | GGCAGTGGTAGCGCA[C/T]GCCTTTAATCCCAGC | 14697 |
rs30222952 | snp | C/G | 0.375 | 0.216506 | intron-variant, nc-transcript-variant | Gnb5, LOC102636700 | Mm_Celera | 9:75310407 | TACTGACCTCACCAA[C/G]GGGCCAAGACCTGGG | 14697 |
rs30241458 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Gnb5, LOC102636700 | Mm_Celera | 9:75310952 | GTTTAGTGGGCAAAG[A/G]CCCCTGCCATCAAGA | 14697 |
rs30262544 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Gnb5 | Mm_Celera | 9:75342117 | CCCCACACACCATAC[A/G]CATGCACACACACAG | 14697 |
rs30271217 | snp | A/T | 0.46875 | 0.121031 | utr-variant-3-prime, upstream-variant-2KB, intron-variant, nc-transcript-variant | Myo5c, Gnb5 | GRCm38.p3 | 9:75304834 | ATCTTTTTTCTGAAA[A/T]TTTTAAAACTTGTTA | 14697 |
rs30424888 | snp | C/T | 0.5 | 0 | intron-variant | Gnb5 | Mm_Celera | 9:75317321 | GGTAATGCAGGCCTC[C/T]TACGACTCCAGCACT | 14697 |
rs30436781 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Gnb5 | Mm_Celera | 9:75319183 | GCTGGGGGAGCTTTA[C/T]CCAGACTCTTCGCTC | 14697 |
rs30439314 | snp | A/G | 0.498615 | 0.0262793 | intron-variant | Gnb5 | Mm_Celera | 9:75309524 | GTTACCTTTTGTGCT[A/G]TAACTCGCTCTTCAT | 14697 |
rs30478992 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Gnb5 | Mm_Celera | 9:75330852 | ACCAAGCATTCACAC[A/C]CATGAGTCTATGGGG | 14697 |
rs30492405 | snp | C/T | 0.429688 | 0.173817 | intron-variant | Gnb5 | Mm_Celera | 9:75320161 | TCAAAAAGAACCTGC[C/T]GGCTTCCATGTGCTG | 14697 |
rs32951444 | snp | A/C | 0.32 | 0.24 | intron-variant | Gnb5 | Mm_Celera | 9:75309554 | TGCAAGCCTAGCAAT[A/C]GACATGATATCTCTG | 14697 |
rs32951446 | snp | A/T | 0.142012 | 0.225474 | intron-variant | Gnb5 | Mm_Celera | 9:75309783 | TGCAAGTCAACCCTT[A/T]GCCCAACTGCACAGC | 14697 |
rs32951448 | snp | C/T | 0.32 | 0.24 | intron-variant | Gnb5 | Mm_Celera | 9:75309807 | GCACAGCTTCTAGTT[C/T]CTTCTCTGGCCCTGT | 14697 |
rs32951450 | snp | A/G | 0.142012 | 0.225474 | intron-variant, downstream-variant-500B | Gnb5, LOC102636700 | Mm_Celera | 9:75309934 | CAGTCCAGCTCAGGG[A/G]TGATTTCCTTGAATC | 14697 |
rs32951452 | snp | A/C | 0.32 | 0.24 | intron-variant, downstream-variant-500B | Gnb5, LOC102636700 | Mm_Celera | 9:75309983 | GAGCAGCTATGAAAT[A/C]AGCAGGACAGAGCTG | 14697 |
rs32951974 | snp | C/T | 0.42 | 0.183303 | intron-variant | Gnb5 | Mm_Celera | 9:75321224 | ACTGTTGTATAAAGC[C/T]TTCCACCCATGCCAA | 14697 |
rs32951976 | snp | G/T | 0.489796 | 0.070696 | intron-variant | Gnb5 | Mm_Celera | 9:75321332 | AAAGAAGGGAGAGAG[G/T]TTCCCACCTGTCTTT | 14697 |
rs32951978 | snp | A/C | 0.375 | 0.216506 | intron-variant | Gnb5 | Mm_Celera | 9:75321368 | ACCCCTGTTCTTATG[A/C]CTCCTTTAAATTCAG | 14697 |
rs32951980 | snp | C/T | 0.473373 | 0.11227 | intron-variant | Gnb5 | Mm_Celera | 9:75321371 | CCTGTTCTTATGCCT[C/T]CTTTAAATTCAGGCT | 14697 |
rs32951982 | snp | A/G/T | 0.277778 | 0.248452 | intron-variant | Gnb5 | Mm_Celera | 9:75321392 | AATTCAGGCTCTCAT[A/G/T]GCCTGCCAGCCAGGA | 14697 |
rs32952274 | snp | A/G | 0.32 | 0.24 | intron-variant, downstream-variant-500B | Gnb5, LOC102636700 | Mm_Celera | 9:75310013 | GGCTGCTCCCTATTA[A/G]CCTCCCAGTCCTCCA | 14697 |
rs32952276 | snp | C/T | 0.124444 | 0.216185 | intron-variant, downstream-variant-500B | Gnb5, LOC102636700 | Mm_Celera | 9:75310207 | TGTCCTCTTCCTTCC[C/T]AAGGCTGCTGTTGCT | 14697 |
rs32952278 | snp | A/T | 0.32 | 0.24 | intron-variant | Gnb5, LOC102636700 | Mm_Celera | 9:75311158 | TCCAAGGATCCGTTG[A/T]AAGCATGATTTGTAA | 14697 |
rs32952280 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Gnb5, LOC102636700 | Mm_Celera | 9:75311318 | AAGAGAAGGAGGCTC[C/T]GGTCTCCAGAAGCAC | 14697 |
rs32952282 | snp | C/T | 0.32 | 0.24 | intron-variant | Gnb5, LOC102636700 | Mm_Celera | 9:75311790 | GGGGCTCTCTAAGGG[C/T]CATGTGAAGTCATGG | 14697 |
rs32952283 | snp | A/C | 0.32 | 0.24 | intron-variant | Gnb5, LOC102636700 | Mm_Celera | 9:75311870 | TTTTTGCATCTGTCT[A/C]CTCCCAGTCTACCTA | 14697 |
rs32952804 | snp | C/G | 0.46875 | 0.121031 | intron-variant | Gnb5 | Mm_Celera | 9:75321502 | TTGCCCTGTCTGATG[C/G]TTCCAGACTGTGCAC | 14697 |
rs32952806 | snp | C/T | 0.497041 | 0.0383476 | intron-variant | Gnb5 | Mm_Celera | 9:75321814 | TAGAGACACCGTGGG[C/T]GCAGGTCAGGGAACA | 14697 |
rs32952808 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Gnb5 | Mm_Celera | 9:75321940 | TGTTCTGCCAAAGAG[C/T]GGAGTCCCCTGACCG | 14697 |
rs32952810 | snp | C/T | 0.18 | 0.24 | intron-variant | Gnb5 | Mm_Celera | 9:75322073 | CCCGTGGAGAACAAC[C/T]GTTTTAGGTGTACAA | 14697 |
rs32952811 | snp | C/G | 0.459184 | 0.136902 | intron-variant | Gnb5 | Mm_Celera | 9:75322291 | CTCTGTGCCAGGCTT[C/G]AGTAGCTAGCAAGAA | 14697 |
rs32952812 | snp | A/T | 0.142012 | 0.225474 | intron-variant | Gnb5 | Mm_Celera | 9:75322411 | GCAGGTGGCTCAAGC[A/T]GAACACACCGCTATC | 14697 |
rs32952985 | snp | A/C | 0.260355 | 0.249785 | intron-variant, upstream-variant-2KB | Gnb5, LOC102636700 | Mm_Celera | 9:75312953 | ACAGAGACATAGGGA[A/C]TAAAGATGGTTGGTG | 14697 |
rs32952987 | snp | A/G | 0.165289 | 0.235211 | intron-variant, upstream-variant-2KB | Gnb5, LOC102636700 | Mm_Celera | 9:75313464 | GGAGGAGGCCTAAGT[A/G]GAAACCTATCTGTGA | 14697 |
rs32952988 | snp | G/T | 0.35503 | 0.226867 | intron-variant, upstream-variant-2KB | Gnb5, LOC102636700 | Mm_Celera | 9:75313536 | TGGAAGTGTGACACC[G/T]AGTGATCATGGCCCT | 14697 |
rs32952990 | snp | A/G | 0.132653 | 0.220748 | intron-variant, upstream-variant-2KB | Gnb5, LOC102636700 | Mm_Celera | 9:75313656 | ACTGTTGCTGGAGAG[A/G]AGCCGCTGGAGTTAT | 14697 |
rs32952992 | snp | G/T | 0.486111 | 0.0821678 | intron-variant, utr-variant-5-prime, nc-transcript-variant | Gnb5, LOC102636700 | Mm_Celera | 9:75314254 | TTGCGTTTCTCTCCC[G/T]GCTGCATCCGGACGA | 14697 |
rs32953574 | snp | C/T | 0.459184 | 0.136902 | synonymous-codon, nc-transcript-variant | Gnb5 | Mm_Celera | 9:75334190 | GGATAATAAGTGCTC[C/T]GTGTATCCACTGACA | 14697 |
rs32953576 | snp | C/T | 0.244898 | 0.249948 | synonymous-codon, nc-transcript-variant | Gnb5 | Mm_Celera | 9:75334208 | GTATCCACTGACATT[C/T]GACAAGAACGAGAAC | 14697 |
rs32953578 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Gnb5 | Mm_Celera | 9:75334480 | GTCGAGTTGAGACAA[A/G]CTCTGGCTGTTGGCT | 14697 |
rs32953580 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Gnb5 | Mm_Celera | 9:75334576 | ATGGCTGCTGAGCTG[C/T]AGGCCTGTGCActgc | 14697 |
rs32953582 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Gnb5 | Mm_Celera | 9:75335058 | CCACAGCAGGGGCAG[C/T]ACAGCTCCAACACTC | 14697 |
rs32953654 | snp | C/T | 0.495868 | 0.0452663 | intron-variant | Gnb5 | Mm_Celera | 9:75323423 | AGACATCTCAGTAGC[C/T]TGTGACAGTTGTTCC | 14697 |
rs32953656 | snp | G/T | 0.375 | 0.216506 | intron-variant | Gnb5 | Mm_Celera | 9:75323485 | CCGTATAGATTTCAT[G/T]TGTGCGTGGCTGCTT | 14697 |
rs32953658 | snp | A/C | 0.197531 | 0.244432 | intron-variant | Gnb5 | Mm_Celera | 9:75323648 | CACAGCACAGCACCA[A/C]GGGGCACAGCACAGC | 14697 |
rs32953660 | snp | C/G | 0.493827 | 0.0552116 | intron-variant | Gnb5 | Mm_Celera | 9:75323758 | TTAGTGTTTGACTTG[C/G]AAAGAAAGTTTGAAG | 14697 |
rs32953662 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Gnb5 | Mm_Celera | 9:75323807 | TAGAGCCAACATTGG[A/G]ACCCCAAGAAAGAAA | 14697 |
rs32953744 | snp | A/G | 0.165289 | 0.235211 | intron-variant, upstream-variant-2KB | Gnb5, LOC102636700 | Mm_Celera | 9:75314965 | AGGCCTCAGCCTTTT[A/G]AATTCCATTTGGAGA | 14697 |
rs32953746 | snp | G/T | 0.142012 | 0.225474 | intron-variant, upstream-variant-2KB | Gnb5, LOC102636700 | Mm_Celera | 9:75315045 | CTTGCTGGAAGTACA[G/T]AACCCTGGTTGTGTC | 14697 |
rs32953748 | snp | C/T | 0.375 | 0.216506 | intron-variant, upstream-variant-2KB | Gnb5, LOC102636700 | Mm_Celera | 9:75315188 | TAACAAGATAAGGTC[C/T]GGTGCAGCTAGATTG | 14697 |
rs32953750 | snp | C/T | 0.336735 | 0.234472 | intron-variant, upstream-variant-2KB | Gnb5, LOC102636700 | Mm_Celera | 9:75315458 | GTGACACAGGGTCTG[C/T]CTTCTCAGAGCCTTG | 14697 |
rs32953752 | snp | A/T | 0.42 | 0.183303 | intron-variant, upstream-variant-2KB | Gnb5, LOC102636700 | Mm_Celera | 9:75315518 | CAGGCTTGGTATCCC[A/T]GCCTTGGACTTCTCC | 14697 |
rs32954004 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Gnb5 | Mm_Celera | 9:75344108 | TTCCATGCCTTCCCC[A/G]GAAGACAATGACTAC | 14697 |
rs32954006 | snp | G/T | 0.336735 | 0.234472 | utr-variant-3-prime, nc-transcript-variant | Gnb5 | Mm_Celera | 9:75344979 | ATCTTCTGACAGCGT[G/T]CAAGAATGTGTGTCC | 14697 |
rs32954008 | snp | A/G | 0.231111 | 0.249285 | utr-variant-3-prime, nc-transcript-variant | Gnb5 | Mm_Celera | 9:75345318 | GTACCTTTTCTTGGC[A/G]TGGACTGTGGCTTCT | 14697 |
rs32954010 | snp | A/G | 0.231111 | 0.249285 | utr-variant-3-prime, nc-transcript-variant | Gnb5 | Mm_Celera | 9:75345609 | AATTCACTTGTGATC[A/G]ATGGCAGTCTAGGCT | 14697 |