All variants in the EGFR gene

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

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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.3551A>G r.(?) p.(Asn1184Ser) - VUS g.55273228A>G g.55205535A>G EGFR(NM_005228.3):c.3551A>G (p.N1184S) - EGFR_000030 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - VKGL-NL_Rotterdam
-?/. - c.3551A>G r.(?) p.(Asn1184Ser) - likely benign g.55273228A>G g.55205535A>G EGFR(NM_005228.3):c.3551A>G (p.N1184S) - EGFR_000030 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - VKGL-NL_VUmc
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