ClinVar Miner

List of variants in gene EGFR reported as likely benign by CeGaT Center for Human Genetics Tuebingen

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 22
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HGVS dbSNP gnomAD frequency
NM_005228.5(EGFR):c.3015A>G (p.Glu1005=) rs55737335 0.00247
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.3225C>T (p.Gly1075=) rs140117937 0.00032
NM_005228.5(EGFR):c.1851C>T (p.Cys617=) rs143422127 0.00010
NM_005228.5(EGFR):c.2457G>A (p.Val819=) rs56183713 0.00010
NM_005228.5(EGFR):c.3087G>A (p.Thr1029=) rs141489713 0.00009
NM_005228.5(EGFR):c.1774G>A (p.Val592Ile) rs144943614 0.00007
NM_005228.5(EGFR):c.2019C>T (p.Ile673=) rs763193362 0.00005
NM_005228.5(EGFR):c.768C>T (p.Asp256=) rs146098757 0.00004
NM_005228.5(EGFR):c.339C>T (p.Tyr113=) rs374582814 0.00003
NM_005228.5(EGFR):c.21C>T (p.Ala7=) rs369581368 0.00002
NM_005228.5(EGFR):c.30G>T (p.Ala10=) rs757936561 0.00001
NM_005228.5(EGFR):c.1881-658G>A
NM_005228.5(EGFR):c.1881-670T>G
NM_005228.5(EGFR):c.2223C>T (p.Pro741=) rs372772241
NM_005228.5(EGFR):c.2496C>T (p.Arg832=)
NM_005228.5(EGFR):c.2946+371G>A
NM_005228.5(EGFR):c.2976T>C (p.Pro992=)
NM_005228.5(EGFR):c.3057A>C (p.Pro1019=)
NM_005228.5(EGFR):c.3271+26C>T
NM_005228.5(EGFR):c.828G>A (p.Gln276=) rs2128935031

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