Variant #0000614041 (NC_000012.11:g.25398229G>A, KRAS(NM_004985.3):c.90C>T)
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.25398229G>A |
DNA change (hg38) |
g.25245295G>A |
Published as |
KRAS(NM_033360.4):c.90C>T (p.D30=) |
ISCN |
- |
DB-ID |
LYRM5_000014 |
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) |
0.0002 View details |
Owner |
VKGL-NL_AMC |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_AMC |

Variant on transcripts
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