Variant #0000811016 (NC_000011.9:g.533885_533893dup, HRAS(NM_005343.2):c.164_172dup)

Individual ID 00383171
Chromosome 11
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.533885_533893dup
DNA change (hg38) g.533885_533893dup
Published as -
ISCN -
DB-ID HRAS_000021
Variant remarks -
Reference 2021, submitted
ClinVar ID -
dbSNP ID -
Origin Germline
Segregation -
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (gnomAD v.2.1.1) Variant not found in online data sets
Owner Yoko Aoki
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Yoko Aoki
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HRAS NM_005343.2 +/. - c.164_172dup r.(?) p.(Ile55_Asp57dup)



Screenings


AscendingScreening ID     

Template     

Technique     

Tissue     

Remarks     

Genes screened     

Variants found     

Owner     
0000384396 DNA SEQ - - HRAS 1 Yoko Aoki