C40A11.2
SNP - dbSNP
dbSNPTypeAllelesHetSe(het)Fxn-classGene NameAssemblyChr-posSequenceEntrez Gene
rs193582331snpC/Tsynonymous-codon?WS195II:2147014CGGTGGTACGGTATT[C/T]GAGACGTGTAAACTG183352
rs193582332snpA/Cmissense?WS195II:2147057TTTGATGGTTTCTTC[A/C]AAACTATGCTCACAA183352
rs193582333snpA/Cmissense?WS195II:2147381AAAATATCTGAAAGA[A/C]GGTGATGACGTGGAA183352
rs193582334snpC/Tsynonymous-codon?WS195II:2147510TCGGTCATATGAAAC[C/T]TCGGAGGAGCTTCTT183352
rs193582335snpC/Tsynonymous-codon?WS195II:2147534GCTTCTTCATATTAT[C/T]GCAAACTGCAAAAAG183352
rs193582336snpA/Gintron-variant?WS195II:2148454CTGATTGGTCGAAAA[A/G]TGGGCGTGGCCGGGC183352
rs193582337snpA/Gintron-variant?WS195II:2148485GCTGATTGGTCGAAT[A/G]ATTTACAAGTGATTT183352
rs193582338snpA/Cintron-variant?WS195II:2148753ATTTTCATTATAAAA[A/C]AAATGTAAAAAATTT183352
rs353097323snpC/Tmissense?WS195II:2148537GATGAATCTGATAAA[C/T]CTCGGCGTGAAGATG183352
rs353099182snpA/Gsynonymous-codon?WS195II:2148608CTCTCCGATTAAAGG[A/G]TTTAAAACATTTACA183352
rs353101656snpA/Gsynonymous-codon?WS195II:2147405CGTGGAACTTCCAAA[A/G]TTTGAACGAGAACTG183352
rs353101745snpC/Tintron-variant?WS195II:2148677GTGAAAATCGGGAAT[C/T]TATGAATAAAATGTT183352
rs353102695snpC/Tsynonymous-codon?WS195II:2147330ATCCGGGTGCATTTT[C/T]GTGGATCGGTCCCCG183352
rs353108681snpA/Tsynonymous-codon?WS195II:2148325TCAGACAGCAATTCT[A/T]GTGATCAGCTATACA183352
rs353109598snpA/Gintron-variant?WS195II:2148009TTTAAAATGTTTAGC[A/G]CGAAATTCAAAAATC183352
rs353111328in-del-/Tintron-variant?WS195II:2147238CTACAACTTTCGAAA[-/T]CTTTCTCAAAGCTTC183352
rs353115020snpC/Tsynonymous-codon?WS195II:2148397TTTTCAATATGTTCT[C/T]GAAAATCCAAAGTTG183352
rs353126869snpA/Gmissense?WS195II:2148559GTGAAGATGGAGTCA[A/G]TAAAGGTCACCAATC183352
rs353129140snpC/Gintron-variant?WS195II:2148131AAATGGGCGGGCGGG[C/G]TGAGCTCCGCCCACT183352
rs353129383snpA/Cmissense?WS195II:2148612CCGATTAAAGGATTT[A/C]AAACATTTACAAATT183352
rs353132907snpA/Cmissense?WS195II:2147349GATCGGTCCCCGAAA[A/C]ATTTCAGCCTGATTC183352
rs353134766snpA/Gintron-variant?WS195II:2147575CGTCATTGAGTGGGC[A/G]GGGCTTTAGAGGCCA183352
rs353137701snpA/Gsynonymous-codon?WS195II:2147456CGAATTTTACCTTTT[A/G]GACGGTCTAGTCGAC183352
rs353139197snpC/Gintron-variant?WS195II:2148093CCCACTAAAGAGGCG[C/G]GACGGGATTGGCTCC183352
rs353139500snpC/Tsynonymous-codon?WS195II:2148403ATATGTTCTCGAAAA[C/T]CCAAAGTTGGATGTC183352
rs353141983snpA/Gmissense?WS195II:2148350TATACAGTTCACAAT[A/G]ATCACCTCTGGAACT183352
rs353146905snpC/Tintron-variant?WS195II:2147770AAAAATTTTATAGAA[C/T]TTTCAGAAAAAATTT183352
rs353148226snpA/Gintron-variant?WS195II:2147832TGACAGTTTTCAGCT[A/G]ATTTTGTAATTTTTA183352
rs353151004in-del-/Aintron-variant?WS195II:2147961TTGTGGGCGGAGCTT[-/A]AATAAGCCACACCCA183352
rs353153755snpA/Gmissense?WS195II:2147388CTGAAAGAAGGTGAT[A/G]ACGTGGAACTTCCAA183352
rs353157222snpA/Tmissense?WS195II:2148563AGATGGAGTCAATAA[A/T]GGTCACCAATCATGG183352
rs353159553snpA/Tmissense?WS195II:2148632ATTTACAAATTTTGA[A/T]AAATTGGAGAAATAT183352
rs353162196snpG/Tsynonymous-codon?WS195II:2147489ATGTGATTCTTTTCT[G/T]AAAATTCGGTCATAT183352
rs353163041snpA/Tintron-variant?WS195II:2147759CTAAATGTTTAAAAA[A/T]TTTTATAGAATTTTC183352
rs353166991snpC/Tintron-variant?WS195II:2147839TTTCAGCTGATTTTG[C/T]AATTTTTATGAAATG183352
rs353169995snpG/Tmissense?WS195II:2148626TAAAACATTTACAAA[G/T]TTTGATAAATTGGAG183352
rs353171891snpA/Gintron-variant?WS195II:2147801CAGAAATGTTCTGGG[A/G]CTCATTGAAACTTTC183352
rs353175630snpC/Tintron-variant?WS195II:2148434TATTTCAGTGAGTTT[C/T]TGACCTGATTGGTCG183352
rs353177520snpA/Cmissense?WS195II:2148375GGAACTCTCCAGAAT[A/C]CTTCAATTTTCAATA183352
rs353180528snpA/Gintron-variant?WS195II:2148095CACTAAAGAGGCGGG[A/G]CGGGATTGGCTCCGC183352
Full records
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