Variant #0000278621 (NC_000012.11:g.25362854C>T, KRAS(NM_004985.3):c.451-9G>A)

Chromosome 12
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.25362854C>T
DNA change (hg38) g.25209920C>T
Published as KRAS(NM_004985.3):c.451-9G>A (p.(=)), KRAS(NM_033360.4):c.*5-9G>A
ISCN -
DB-ID KRAS_000034 See all 2 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) 0.02381 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
LYRM5 NM_001001660.2 -/. - c.*5608C>T r.(=) p.(=)
KRAS NM_004985.3 -/. - c.451-9G>A r.(=) p.(=)