Variant #0000343933 (NC_000012.11:g.25362838T>A, KRAS(NM_004985.3):c.458A>T)

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.25362838T>A
DNA change (hg38) g.25209904T>A
Published as -
ISCN -
DB-ID KRAS_000019
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) Variant not found in online data sets
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
LYRM5 NM_001001660.2 +/. - c.*5592T>A r.(=) p.(=)
KRAS NM_004985.3 +/. - c.458A>T r.(?) p.(Asp153Val)