Chr Mutation (hg38) CAid Gene Transcript Linkouts
14g.28767968G>TCA10606123FOXG1c.689G>T (p.Arg230Leu)
 ClinVar dbSNP
14g.28767968G>ACA199440FOXG1c.689G>A (p.Arg230His)
 ClinVar dbSNP COSMIC
14g.28767968G=CA2125999994FOXG1c.689G= (p.Arg230=)
 dbSNP

Number of alleles fetched