Variant #0000547650 (NC_000012.11:g.25368405A>T, NC_000012.11(NM_004985.3):c.451-5560T>A (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.25368405A>T
DNA change (hg38) g.25215471A>T
Published as KRAS(NM_033360.2):c.540T>A (p.(Cys180*)), KRAS(NM_033360.4):c.540T>A (p.C180*)
ISCN -
DB-ID LYRM5_000005 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 -
Methylation -
Average frequency (gnomAD v.2.1.1) 8.0E-5 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-07-07 10:10:56 +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.*11159A>T r.(=) p.(=)
KRAS NM_004985.3 ?/. - c.451-5560T>A r.(=) p.(=)


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