Variant #0000339763 (NC_000012.11:g.25398295T>C, KRAS(NM_004985.3):c.24A>G)
Chromosome |
12 |
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.25398295T>C |
DNA change (hg38) |
g.25245361T>C |
Published as |
KRAS(NM_033360.3):c.24A>G (p.V8=), KRAS(NM_033360.4):c.24A>G (p.V8=) |
ISCN |
- |
DB-ID |
KRAS_000033 See all 4 reported entries |
Variant remarks |
VKGL data sharing initiative Nederland |
Reference |
- |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
CLASSIFICATION record |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
0 |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
0.00024 View details |
Owner |
VKGL-NL_Nijmegen |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Nijmegen |

Variant on transcripts
|
|