Chr Mutation (hg38) CAid Gene Transcript Linkouts
7g.55181321_55181322insGATACAACCCCCACGTGTGCA2714511593EGFR,EGFR-AS1c.2153_2154insGATACAACCCCCACGTGTG (p.Asn718LysfsTer?)
c.661_662insGATACAACCCCCACGTGTG
c.2312_2313insGATACAACCCCCACGTGTG (p.Asn771LysfsTer?)
c.*28+8393_*28+8394insGATACAACCCCCACGTGTG (n.*28+8393_*28+8394insGATACAACCCCCACGTGTG)
c.2177_2178insGATACAACCCCCACGTGTG (p.Asn726LysfsTer?)
n.1249_1250insCACACGTGGGGGTTGTATC
c.1511_1512insGATACAACCCCCACGTGTG (p.Asn504LysfsTer?)
 dbSNP
7g.55181321_55181322insACTCA645561599EGFR,EGFR-AS1c.2153_2154insACT (p.Asn718delinsLysLeu)
c.661_662insACT
c.2312_2313insACT (p.Asn771delinsLysLeu)
c.*28+8393_*28+8394insACT (n.*28+8393_*28+8394insACT)
c.2177_2178insACT (p.Asn726delinsLysLeu)
n.1249_1250insAGT
c.1511_1512insACT (p.Asn504delinsLysLeu)
 dbSNP COSMIC
7g.55181321_55181322insGCCCCACGTGTGCA2714511591EGFR,EGFR-AS1c.2153_2154insGCCCCACGTGTG (p.Asn718delinsLysProHisValCys)
c.661_662insGCCCCACGTGTG
c.2312_2313insGCCCCACGTGTG (p.Asn771delinsLysProHisValCys)
c.*28+8393_*28+8394insGCCCCACGTGTG (n.*28+8393_*28+8394insGCCCCACGTGTG)
c.2177_2178insGCCCCACGTGTG (p.Asn726delinsLysProHisValCys)
n.1249_1250insCACACGTGGGGC
c.1511_1512insGCCCCACGTGTG (p.Asn504delinsLysProHisValCys)
 dbSNP
7g.55181321_55181322insTGTCA176017EGFR,EGFR-AS1c.2153_2154insTGT (p.Asn718_Pro719insVal)
c.661_662insTGT
c.2312_2313insTGT (p.Asn771_Pro772insVal)
c.*28+8393_*28+8394insTGT (n.*28+8393_*28+8394insTGT)
c.2177_2178insTGT (p.Asn726_Pro727insVal)
n.1249_1250insACA
c.1511_1512insTGT (p.Asn504_Pro505insVal)
 ClinVar dbSNP
7g.55181321_55181322insTCCCCACGTGTGCA2714511592EGFR,EGFR-AS1c.2153_2154insTCCCCACGTGTG (p.Asn718_Pro719insProHisValCys)
c.661_662insTCCCCACGTGTG
c.2312_2313insTCCCCACGTGTG (p.Asn771_Pro772insProHisValCys)
c.*28+8393_*28+8394insTCCCCACGTGTG (n.*28+8393_*28+8394insTCCCCACGTGTG)
c.2177_2178insTCCCCACGTGTG (p.Asn726_Pro727insProHisValCys)
n.1249_1250insCACACGTGGGGA
c.1511_1512insTCCCCACGTGTG (p.Asn504_Pro505insProHisValCys)
 dbSNP

Number of alleles fetched