Variant #0000547654 (NC_000012.11:g.25380247A>G, KRAS(NM_004985.3):c.211T>C)

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.25380247A>G
DNA change (hg38) g.25227313A>G
Published as KRAS(NM_004985.3):c.211T>C (p.(Tyr71His))
ISCN -
DB-ID LYRM5_000009
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) Variant not found in online data sets
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
LYRM5 NM_001001660.2 +/. - c.*23001A>G r.(=) p.(=)
KRAS NM_004985.3 +/. - c.211T>C r.(?) p.(Tyr71His)