W07E6.2
SNP - dbSNP
dbSNPTypeAllelesHetSe(het)Fxn-classGene NameAssemblyChr-posSequenceEntrez Gene
rs193323464snpG/T0.4012350.199068intron-variant?WS195II:481136GAAAATCGTTCGAAA[G/T]TTGTAGATTGTAGTC173439
rs193323465snpC/T0.3996850.200236intron-variant?WS195II:483333CTGCTAGACTACAAA[C/T]TACAAATTTCGATTT173439
rs193323466snpA/C0.01036240.0712308intron-variant?WS195II:483339GACTACAAATTACAA[A/C]TTTCGATTTAGCAGA173439
rs193580166snpA/Tintron-variant?WS195II:481274AGGCTCAAAGTAGGT[A/T]ATTCTGACTGAAAAT173439
rs193580167snpC/Tmissense?WS195II:481626CGCCGCCGGCAATTT[C/T]CAGAGCTGCTTCATA173439
rs193580168snpA/Cintron-variant?WS195II:481790GCATGGCGTCCGCGT[A/C]CCCGGTGACAAATGT173439
rs193580169snpA/Tintron-variant?WS195II:482225CCGCATGAAAACCTA[A/T]AGATGTAGACTAGTC173439
rs193580170snpC/Tintron-variant?WS195II:482370AGAGTAGGAAATTGA[C/T]GTTTCCAGTAGAAAA173439
rs193580171snpA/Cmissense?WS195II:483013CTACAGTACCCTGTA[A/C]GGTATCCCAAATGAA173439
rs193580172snpA/Cintron-variant?WS195II:484069ATTTTAAATTTTTTA[A/C]AAAGTTTTCTATCTT173439
rs193580173snpC/Tsynonymous-codon?WS195II:484282AATTTGCAGCTCATT[C/T]GTGGAGATGTCCACT173439
rs353096952snpA/Gintron-variant?WS195II:482065CTGCGTTTAAATAGA[A/G]ACAACAATCTGCTAA173439
rs353109658snpC/Tmissense?WS195II:483806CAACTTTTATGGGAT[C/T]TACACGTGTGGAGAG173439
rs353126200snpC/Tintron-variant?WS195II:482348AATTACAATTTTTCT[C/T]GTTTTTAGAGTAGGA173439
rs353132227in-del-/Aintron-variant?WS195II:482684TGAAATTTATGTTTT[-/A]AAAAAATTCGAAATT173439
rs353134624snpA/Gintron-variant?WS195II:482104TTCGAAATTTTGGAA[A/G]AATCTGACCAAAAGT173439
rs353137201snpA/Tintron-variant?WS195II:482432ATGGAAAAAAAACGG[A/T]AAACTCCAAATTTTC173439
rs353139240snpA/Cintron-variant?WS195II:483957TTTAAATGCGTCAAA[A/C]CGATCAAAAAATTAC173439
rs353142898snpA/Gintron-variant?WS195II:482144GCATATTCTGAATAG[A/G]AAATTAAAATTTTTA173439
rs353167018snpA/Tintron-variant?WS195II:482684TGAAATTTATGTTTT[A/T]AAAAAATTCGAAATT173439
rs353167740in-del-/Tintron-variant?WS195II:483202AGAGAAAAACTCGGG[-/T]TTTCTGAAGCTTTCT173439
Full records
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