Variant #0000000279 (NC_000012.11:g.25359841T>C, NM_004985.3:c.*2888A>G (KRAS))
Individual ID |
00000029 |
Chromosome |
12 |
Allele |
Parent #1 |
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.25359841T>C |
DNA change (hg38) |
g.25206907T>C |
Published as |
- |
ISCN |
- |
DB-ID |
KRAS_000011 |
Variant remarks |
- |
Reference |
PubMed: Almomani 2011 |
ClinVar ID |
- |
dbSNP ID |
rs13096 |
Origin |
Germline |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
Retrieve |
Owner |
Gerard C.P. Schaafsma |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
Gerard C.P. Schaafsma |
Date created |
2012-05-01 14:55:35 +02:00 (CEST) |
Date last edited |
2018-08-25 03:31:14 +02:00 (CEST) |

Variant on transcripts
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