Variant #0000999912 (NC_000012.11:g.25368369A>C, NC_000012.11(NM_004985.3):c.451-5524T>G (KRAS))

Chromosome 12
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.25368369A>C
DNA change (hg38) -
Published as KRAS(NM_033360.2):c.*4+2T>G (p.?)
ISCN -
DB-ID LYRM5_000027
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
LYRM5 NM_001001660.2 ?/. - c.*11123A>C r.(=) p.(=)
KRAS NM_004985.3 ?/. - c.451-5524T>G r.(=) p.(=)


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