Variant #0000547653 (NC_000012.11:g.25380244T>G, KRAS(NM_004985.3):c.214A>C)

Chromosome 12
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.25380244T>G
DNA change (hg38) g.25227310T>G
Published as -
ISCN -
DB-ID LYRM5_000008
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_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.*22998T>G r.(=) p.(=)
KRAS NM_004985.3 +?/. - c.214A>C r.(?) p.(Met72Leu)