Chr Mutation (hg38) CAid Gene Transcript Linkouts
7g.55181402T>CCA367578906EGFR,EGFR-AS1c.2234T>C (p.Leu745Pro)
c.742T>C
c.2393T>C (p.Leu798Pro)
c.*28+8474T>C (n.*28+8474T>C)
c.2258T>C (p.Leu753Pro)
n.1169A>G
c.1592T>C (p.Leu531Pro)
dbSNP
7g.55181402T>ACA151175EGFR,EGFR-AS1c.2234T>A (p.Leu745His)
c.742T>A
c.2393T>A (p.Leu798His)
c.*28+8474T>A (n.*28+8474T>A)
c.2258T>A (p.Leu753His)
n.1169A>T
c.1592T>A (p.Leu531His)
ClinVar dbSNP COSMIC

Number of alleles fetched