Variant #0000532254 (NC_000007.13:g.55268949A>G, NM_005228.3:c.3015A>G (EGFR))

Chromosome 7
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.55268949A>G
DNA change (hg38) g.55201256A>G
Published as EGFR(NM_001346899.1):c.2880A>G (p.E960=), EGFR(NM_005228.3):c.3015A>G (p.(=)), EGFR(NM_005228.5):c.3015A>G (p.E1005=)
ISCN -
DB-ID EGFR_000023 See all 3 reported entries
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00227 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-11-27 17:27:23 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
EGFR NM_005228.3 -?/. - c.3015A>G r.(?) p.(Glu1005=)


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