Variant #0000787502 (NC_000012.11:g.25362805C>T, KRAS(NM_004985.3):c.491G>A)

Individual ID 00374403
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.25362805C>T
DNA change (hg38) g.25209871C>T
Published as -
ISCN -
DB-ID KRAS_000042
Variant remarks -
Reference 0
ClinVar ID -
dbSNP ID rs758575947
Origin Germline
Segregation -
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (gnomAD v.2.1.1) 2.0E-5 View details
Owner LOVD
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
KRAS NM_004985.3 ?/. 5 c.491G>A r.(?) p.(Arg164Gln)



Screenings


AscendingScreening ID     

Template     

Technique     

Tissue     

Remarks     

Genes screened     

Variants found     

Owner     
0000375597 DNA SEQ-NG - TruSight One panel MTHFR 2 Johan den Dunnen