Variant #0000655853 (NC_000007.13:g.55259429G>A, NM_005228.3:c.2487G>A (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.55259429G>A |
DNA change (hg38) |
g.55191736G>A |
Published as |
EGFR(NM_001346899.1):c.2352G>A (p.E784=) |
ISCN |
- |
DB-ID |
EGFR_000034 |
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) |
0.00059 View details |
Owner |
VKGL-NL_Rotterdam |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Rotterdam |
Date created |
2020-03-23 16:13:27 +01:00 (CET) |
Date last edited |
2020-06-22 17:27:58 +02:00 (CEST) |

Variant on transcripts
|