Variant #0000853351 (NC_000012.11:g.25398279C>T, NM_004985.3:c.40G>A (KRAS))

Chromosome 12
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.25398279C>T
DNA change (hg38) -
Published as KRAS(NM_004985.5):c.40G>A (p.(Val14Ile)), KRAS(NM_033360.3):c.40G>A (p.V14I)
ISCN -
DB-ID KRAS_000032 See all 7 reported entries
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) Retrieve
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2022-05-09 15:40:45 +02:00 (CEST)
Date last edited 2024-04-19 20:27:30 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
LYRM5 NM_001001660.2 +/. - c.*41033C>T r.(=) p.(=)
KRAS NM_004985.3 +/. - c.40G>A r.(?) p.(Val14Ile)


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