Variant #0001045030 (NC_000007.13:g.55249013_55249014insGTC, NM_005228.3:c.2311_2312insGTC (EGFR))

Chromosome 7
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.55249013_55249014insGTC
DNA change (hg38) -
Published as -
ISCN -
DB-ID EGFR_000062
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs1554350351
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2025-05-22 15:38:01 +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.2311_2312insGTC r.(?) p.(Asn771delinsSerHis)


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