str-148
SNP - dbSNP
dbSNPTypeAllelesHetSe(het)Fxn-classGene NameAssemblyChr-posSequenceEntrez Gene
rs193323801snpC/T0.3077310.243243synonymous-codonstr-148WS195II:1047983GCCATTATTCGAGGT[C/T]TACGTTGGAAGCATT173486
rs193323802snpA/G0.105490.204002missensestr-148WS195II:1047994AGGTCTACGTTGGAA[A/G]CATTGCGAATTTTGT173486
rs193323803snpA/T0.3077310.243243missensestr-148WS195II:1047996GTCTACGTTGGAAGC[A/T]TTGCGAATTTTGTTG173486
rs193323804snpG/T0.4181920.184963synonymous-codonstr-148WS195II:1048025TGGTGCAAGTCTAGC[G/T]GTCTATCCATCACTT173486
rs193323805snpC/T0.300740.244797synonymous-codonstr-148WS195II:1048088ATTCAGGAAAACTGT[C/T]ACATGTGGGTACAGC173486
rs193323806snpG/T0.01111080.0737016intron-variantstr-148WS195II:1048131CAATTAATTGAACAT[G/T]TTTTAGGTCCCTCAC173486
rs193323807snpC/T0.300740.244797synonymous-codonstr-148WS195II:1048139TGAACATGTTTTAGG[C/T]CCCTCACTTCGAAAG173486
rs193323808snpC/T0.300740.244797missensestr-148WS195II:1048140GAACATGTTTTAGGT[C/T]CCTCACTTCGAAAGG173486
rs193580887snpA/Gintron-variantstr-148WS195II:1046993TTTAAATGTGAATTA[A/G]GGTCTCATGAGGTCG173486
rs193580888snpC/Tintron-variantstr-148WS195II:1047012CTCATGAGGTCGCCG[C/T]ATCGGCGCCCGCGCC173486
rs193580889snpA/Gintron-variantstr-148WS195II:1047260CGTAGTTCGCGCCTC[A/G]CTCAGCTGGGAGCGT173486
rs193580890snpC/Tmissensestr-148WS195II:1047298AATACATATTTCAGA[C/T]CGAATTTTCTGCAAA173486
rs193580892snpA/Gmissensestr-148WS195II:1047631GAACAAATGGTGAGA[A/G]GATTTGGAAGTTTTG173486
rs193580893snpA/Gmissensestr-148WS195II:1047667TTATGTCTTCTGTGG[A/G]ATGTGTTTGTATAAT173486
rs193580894snpC/Tintron-variantstr-148WS195II:1047695AATTGTAAGTACATA[C/T]TTCTGAAATTCATTT173486
rs193580895snpC/Gintron-variantstr-148WS195II:1047903AAATGAAACATGGTT[C/G]ACGATTTTCAGACAA173486
rs193580896snpA/Cintron-variantstr-148WS195II:1047904AATGAAACATGGTTG[A/C]CGATTTTCAGACAAT173486
rs193580897snpG/Tutr-variant-3-primestr-148WS195II:1048229CAAACCCATTAAAAA[G/T]AAATTAAATTGCTTA173486
rs353096173snpC/Tsynonymous-codonstr-148WS195II:1047844TCGCCAACTGTTTAT[C/T]ACTCTTACATTTCAA173486
rs353102119snpA/Gsynonymous-codonstr-148WS195II:1046534GCTGCATATCATACA[A/G]TATTCTGGGTTTTTT173486
rs353108470snpA/Tintron-variantstr-148WS195II:1047194AATGTGTCGGCCGCT[A/T]CAGATAACTAGCTTT173486
rs353110680snpA/Gintron-variantstr-148WS195II:1047173ACGTTAAGCTGCGGA[A/G]CCCTAAATGTGTCGG173486
rs353126113snpA/Tmissensestr-148WS195II:1047325CAAAACATTGAAGGC[A/T]TCAAGTTGACATTTA173486
rs353131844snpA/Gintron-variantstr-148WS195II:1047886TTTTGTGTGTTTTAT[A/G]AAAATGAAACATGGT173486
rs353134727snpA/Gintron-variantstr-148WS195II:1047862TCTTACATTTCAAGT[A/G]AAGTCATTTTTTGTG173486
rs353137139snpC/Tsynonymous-codonstr-148WS195II:1046931AGCTCAATTTTTCTA[C/T]CGTTATGTAGCCATG173486
rs353147076snpC/Tintron-variantstr-148WS195II:1047177TAAGCTGCGGAACCC[C/T]AAATGTGTCGGCCGC173486
rs353153426in-del-/GTintron-variantstr-148WS195II:1046858AACTTTAAAGAATAC[-/GT]AAATCTAATTTTAGG173486
rs353153976snpA/Tsynonymous-codonstr-148WS195II:1046531TTGGCTGCATATCAT[A/T]CAATATTCTGGGTTT173486
rs353159645in-del-/ATATAATintron-variantstr-148WS195II:1047514TGCAATGCAATTTTA[-/ATATAAT]ATAACGTAATGTAAT173486
rs353162022snpC/Tintron-variantstr-148WS195II:1046962TGCAGGTAGATTTTG[C/T]TCAGAAATGAAGTTT173486
rs353162533snpA/Tintron-variantstr-148WS195II:1047114CGCTTCCAAATAACT[A/T]TTTTTCGCACTATGT173486