C16C8.16
SNP - dbSNP
dbSNPTypeAllelesHetSe(het)Fxn-classGene NameAssemblyChr-posSequenceEntrez Gene
rs193325016snpA/G0.4183760.184796missense?WS195II:3445984GATGAGATGAAGCAA[A/G]TTCAGCAGAACGTGA173688
rs193325017snpG/T0.0199980.0979748synonymous-codon?WS195II:3446019GGAGTTGAAATCTGT[G/T]AAAAAAGAACTGAAA173688
rs193325018snpA/G0.02009840.0982103missense?WS195II:3446143CAAAACAAATCGATC[A/G]AAAATTTGAATTCGG173688
rs193325019snpC/T0.03108030.120724intron-variant?WS195II:3446932AATTATCAAAAAGCT[C/T]TTTTTTTTCAGATTT173688
rs193325020snpA/G0.05935030.161718missense?WS195II:3446965AAATGTCGGAGACAA[A/G]CAGTTTGATGTCTCA173688
rs193325021snpC/T0.02019990.0984476missense?WS195II:3447013TTGAAACTTCCAAGA[C/T]ATACAATGAATTCAC173688
rs193325022snpC/T0.2365430.249638synonymous-codon?WS195II:3447588AATTCGAATAATAAT[C/T]TGAAAATGATGCTGA173688
rs193584757snpG/Tmissense?WS195II:3447449ATTGATCGAAAAGTT[G/T]ATGTCGGAATTGAAA173688
rs193584758snpC/Tintron-variant?WS195II:3447910AAATAAAATTTGCAT[C/T]TCAGATAAAATTCTC173688
rs193584759snpA/Tmissense?WS195II:3448412AAGCCCCAATTGAAG[A/T]TAAAAAATTGGATAA173688
rs353101000snpC/Tintron-variant?WS195II:3446686TATTCTAATTTTCAT[C/T]CACTTTTTTCAAGAT173688
rs353102884snpC/Tsplice-donor-variant?WS195II:3447829GCATCAATTCACTTG[C/T]AGGAATAGACATCGG173688
rs353113968in-del-/Gframeshift-variant?WS195II:3447449ATTGATCGAAAAGTT[-/G]ATGTCGGAATTGAAA173688
rs353115031snpA/Gmissense?WS195II:3447681GTCCCAATTGAATCT[A/G]GAGAATTGGCAAAGA173688
rs353119370snpA/Gsynonymous-codon?WS195II:3448356AGGAGAATTTGCGAA[A/G]AAGATCGAAGAATCA173688
rs353122124in-del-/Cframeshift-variant?WS195II:3448706TATCGCTTATTACAA[-/C]ATTCAAGAAGGCTCA173688
rs353122349in-del-/Tintron-variant?WS195II:3446756TTCGCTTTTCACAGA[-/T]TTTTTTTAAAAATGA173688
rs353132296in-del-/Tintron-variant?WS195II:3448103ATAATTTTTTATCGA[-/T]TTTTTTTAAATTATT173688
rs353142065snpA/Gintron-variant?WS195II:3446715ATATTGTTATTTTGC[A/G]AATAAATAATTGTTA173688
rs353142350in-del-/ATintron-variant?WS195II:3447037ATTCACAGAGGTGAG[-/AT]AATAATAATAATAAT173688
rs353146728in-del-/CCintron-variant?WS195II:3448631TTTGTTAGTTTAAAT[-/CC]CCCTTTCTTCATAAT173688
rs353169282in-del-/Tintron-variant?WS195II:3446816CAAAAATAAAAGCAA[-/T]CTTTCTTGGTTTTCG173688
rs353171701in-del-/Aintron-variant?WS195II:3446764TCACAGATTTTTTTT[-/A]AAAATGATTCTGCAA173688
rs353172125snpC/Gmissense?WS195II:3447431CCAGGAAAATGAAAA[C/G]AAATTGATCGAAAAG173688