All variants in the EGFR gene

Information The variants shown are described using the NM_005228.3 transcript reference sequence.

3 entries on 1 page. Showing entries 1 - 3.
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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

Classification method     

Clinical classification     

DNA change (genomic) (hg19)     

DNA change (hg38)     

Published as     

ISCN     

DB-ID     

Variant remarks     

Reference     

ClinVar ID     

dbSNP ID     

Origin     

Segregation     

Frequency     

Re-site     

VIP     

Methylation     

Owner     
-?/. - c.3015A>G r.(?) p.(Glu1005=) - likely benign g.55268949A>G g.55201256A>G EGFR(NM_001346899.1):c.2880A>G (p.E960=), EGFR(NM_005228.3):c.3015A>G (p.(=), p.E1005=) - EGFR_000023 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - 0 - VKGL-NL_VUmc
-?/. - c.3015A>G r.(?) p.(Glu1005=) - likely benign g.55268949A>G g.55201256A>G EGFR(NM_001346899.1):c.2880A>G (p.E960=), EGFR(NM_005228.3):c.3015A>G (p.(=), p.E1005=) - EGFR_000023 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - VKGL-NL_Rotterdam
-?/. - c.3015A>G r.(?) p.(Glu1005=) - likely benign g.55268949A>G g.55201256A>G EGFR(NM_001346899.1):c.2880A>G (p.E960=), EGFR(NM_005228.3):c.3015A>G (p.(=), p.E1005=) - EGFR_000023 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - VKGL-NL_Leiden
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