List of variants in gene EGFR reported as likely pathogenic for nervous system cancer

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 13

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HGVS	dbSNP	gnomAD frequency
NM_005228.5(EGFR):c.1793G>C (p.Gly598Ala)	rs139236063
NM_005228.5(EGFR):c.1793G>T (p.Gly598Val)	rs139236063
NM_005228.5(EGFR):c.2155G>T (p.Gly719Cys)	rs28929495
NM_005228.5(EGFR):c.2156G>A (p.Gly719Asp)	rs121913428
NM_005228.5(EGFR):c.2156G>C (p.Gly719Ala)	rs121913428
NM_005228.5(EGFR):c.322A>G (p.Arg108Gly)	rs1057519888
NM_005228.5(EGFR):c.323G>A (p.Arg108Lys)	rs1057519828
NM_005228.5(EGFR):c.787A>C (p.Thr263Pro)	rs1057519829
NM_005228.5(EGFR):c.865G>A (p.Ala289Thr)	rs769696078
NM_005228.5(EGFR):c.865_866delinsAA (p.Ala289Asn)	rs1057519887
NM_005228.5(EGFR):c.865_866delinsAT (p.Ala289Ile)	rs1057519887
NM_005228.5(EGFR):c.866C>A (p.Ala289Asp)	rs149840192
NM_005228.5(EGFR):c.866C>T (p.Ala289Val)	rs149840192

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