List of variants in gene EGFR reported as uncertain significance for cancer

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 26

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HGVS	dbSNP	gnomAD frequency
NM_005228.5(EGFR):c.3629C>T (p.Ala1210Val)	rs35918369	0.00034
NM_005228.5(EGFR):c.3271+49del	rs17337514	0.00016
NM_005228.5(EGFR):c.3139G>A (p.Val1047Met)	rs142442994	0.00008
NM_005228.5(EGFR):c.1532C>A (p.Ser511Tyr)	rs371114444	0.00007
NM_005228.5(EGFR):c.3092G>A (p.Arg1031Gln)	rs570295933	0.00005
NM_005228.5(EGFR):c.1936A>C (p.Ile646Leu)	rs140516819	0.00004
NM_005228.5(EGFR):c.2270A>G (p.Lys757Arg)	rs397517102	0.00002
NM_005228.5(EGFR):c.116C>T (p.Thr39Met)	rs375919121	0.00001
NM_005228.5(EGFR):c.2305G>A (p.Val769Met)	rs147149347	0.00001
NM_005228.5(EGFR):c.3352G>A (p.Ala1118Thr)	rs770749711	0.00001
NM_005228.5(EGFR):c.59C>A (p.Pro20Gln)	rs1028735720	0.00001
NM_005228.5(EGFR):c.*2368G>T
NM_005228.5(EGFR):c.1661A>G (p.Glu554Gly)	rs779741928
NM_005228.5(EGFR):c.1916A>C (p.Asn639Thr)	rs952307505
NM_005228.5(EGFR):c.2126A>C (p.Glu709Ala)	rs397517085
NM_005228.5(EGFR):c.2126A>G (p.Glu709Gly)	rs397517085
NM_005228.5(EGFR):c.2469+8G>A	rs760763801
NM_005228.5(EGFR):c.2485G>C (p.Glu829Gln)	rs1489158055
NM_005228.5(EGFR):c.2504A>T (p.His835Leu)	rs397517128
NM_005228.5(EGFR):c.2512C>G (p.Leu838Val)	rs864621996
NM_005228.5(EGFR):c.2701+77T>G
NM_005228.5(EGFR):c.3114+101A>G
NM_005228.5(EGFR):c.3272A>C (p.Glu1091Ala)	rs1788061731
NM_005228.5(EGFR):c.3320A>G (p.Asn1107Ser)	rs918187279
NM_005228.5(EGFR):c.676A>C (p.Lys226Gln)	rs2128933753
NM_005228.5(EGFR):c.88+24313G>C

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