Variant #0000927947 (NC_000007.13:g.55249007G>A, NM_005228.3:c.2305G>A (EGFR))

Chromosome 7
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.55249007G>A
DNA change (hg38) -
Published as -
ISCN -
DB-ID EGFR_000048
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs147149347
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 3.0E-5 View details
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2023-07-04 09:42:01 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
EGFR NM_005228.3 ?/. - c.2305G>A r.(?) p.(Val769Met)


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