Variant #0000648528 (NC_000012.11:g.25360224A>C, KRAS(NM_004985.3):c.*2505T>G)

Individual ID 00290671
Chromosome 12
Allele Parent #1
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.25360224A>C
DNA change (hg38) g.25207290A>C
Published as -
ISCN -
DB-ID KRAS_000038 See all 2 reported entries
Variant remarks 102 heterozygous; Clinindb (India)
Reference PubMed: Narang 2020, Journal: Narang 2020
ClinVar ID -
dbSNP ID rs61764370
Origin Germline
Segregation -
Frequency 102/2749 individuals
Re-site -
VIP 0
Methylation -
Average frequency (gnomAD v.2.1.1) Variant not found in online data sets
Owner Mohammed Faruq
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 -?/. - c.*2505T>G r.(=) p.(=)



Screenings


AscendingScreening ID     

Template     

Technique     

Tissue     

Remarks     

Genes screened     

Variants found     

Owner     
0000291839 DNA arraySNP - Infinium Global Screening Array v1.0 - 1 Mohammed Faruq