ClinVar Miner

List of variants in gene EGFR reported as likely benign by Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine

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Gene type:
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Total variants: 22
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HGVS dbSNP gnomAD frequency
NM_005228.5(EGFR):c.2289C>G (p.Ala763=) rs117420095 0.00046
NM_005228.5(EGFR):c.2748C>T (p.Asp916=) rs41396448 0.00046
NM_005228.5(EGFR):c.2355C>T (p.Thr785=) rs148188503 0.00033
NM_005228.5(EGFR):c.2543C>T (p.Pro848Leu) rs148934350 0.00026
NM_005228.5(EGFR):c.2166G>A (p.Ala722=) rs367694667 0.00012
NM_005228.5(EGFR):c.2457G>A (p.Val819=) rs56183713 0.00010
NM_005228.5(EGFR):c.2572C>T (p.Leu858=) rs121913443 0.00003
NM_005228.5(EGFR):c.2280C>T (p.Leu760=) rs397517103 0.00002
NM_005228.5(EGFR):c.2592G>A (p.Ala864=) rs397517131 0.00002
NM_005228.5(EGFR):c.2329C>T (p.Leu777=) rs397517117 0.00001
NM_005228.5(EGFR):c.2484G>A (p.Leu828=) rs727504312 0.00001
NM_005228.5(EGFR):c.2862C>T (p.Asp954=) rs397517138 0.00001
NM_005228.5(EGFR):c.2166G>C (p.Ala722=) rs367694667
NM_005228.5(EGFR):c.2232C>T (p.Ile744=) rs397517093
NM_005228.5(EGFR):c.2310C>T (p.Asp770=) rs397517110
NM_005228.5(EGFR):c.2340C>T (p.Ile780=) rs397517121
NM_005228.5(EGFR):c.2349C>T (p.Thr783=) rs397517122
NM_005228.5(EGFR):c.2409G>A (p.Arg803=) rs397517123
NM_005228.5(EGFR):c.2439C>T (p.Tyr813=) rs397517124
NM_005228.5(EGFR):c.2598G>A (p.Glu866=) rs397517133
NM_005228.5(EGFR):c.2625+6G>T rs397517135
NM_005228.5(EGFR):c.2775C>T (p.Ser925=) rs727504306

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