K02C4.3
SNP - dbSNP
dbSNPTypeAllelesHetSe(het)Fxn-classGene NameAssemblyChr-posSequenceEntrez Gene
rs193326751snpA/G0.07716980.180637missense?WS195II:8082132CATTTTTCGATAAAT[A/G]GAATTCCATGTCAAT174300
rs193326752snpC/T0.44880.151587synonymous-codon?WS195II:8082340CATCGCACAATACGT[C/T]ACTTCGATTTGTTCA174300
rs193326753snpA/G0.02150280.101435intron-variant?WS195II:8082451AGTTTTCCTTTTTAA[A/G]TATAGATTTTTTTGT174300
rs193587769snpC/Tsynonymous-codon?WS195II:8083767CGTATACTTTCGAGG[C/T]GCAATCTTTGTAATC174300
rs353097144snpG/Tintron-variant?WS195II:8082466ATATAGATTTTTTTG[G/T]TTTTTTTTTCATTTT174300
rs353115842snpG/Tintron-variant?WS195II:8081989AACTATTAGGAAATG[G/T]AGATTACTCAGAAAA174300
rs353118099snpA/Gintron-variant?WS195II:8083289GATGAATGAGAAAAG[A/G]CGTGCGCCTTTAAAG174300
rs353120350snpA/Gsynonymous-codon?WS195II:8086114CGGTTGTTCGTGCCA[A/G]CTTAATGGAGCACAG174300
rs353120868in-del-/Tintron-variant?WS195II:8082457CTTTTTAAATATAGA[-/T]TTTTTTTGTTTTTTT174300
rs353145727snpA/Tintron-variant?WS195II:8083029ATACAAAATAAAATT[A/T]AAAAAAAACTTTTTT174300
rs353150137snpA/Cmissense?WS195II:8086978GAAAACGGCGCCAAG[A/C]CTGAAATGTACAAAA174300
rs353160237snpG/Tintron-variant?WS195II:8082465AATATAGATTTTTTT[G/T]TTTTTTTTTTCATTT174300
rs353162535snpA/Gmissense?WS195II:8081833CGTTCTAGGTCCATC[A/G]CGGTGTTCACAACCA174300
rs353175796snpA/Tintron-variant?WS195II:8083030TACAAAATAAAATTA[A/T]AAAAAAACTTTTTTA174300
rs353178013snpA/Cintron-variant?WS195II:8084409TTCATCAAAACTTCA[A/C]ACATAAGGCAGAAAT174300
Full records
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