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 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.*41049T>C r.(=) p.(=)
KRAS NM_004985.3 -?/. - c.24A>G r.(?) p.(Val8=)