Variant #0000008823 (NC_000011.10:g.534242A>G, HRAS(NM_005343.3):c.81T>C)

Individual ID 00001536
Chromosome 11
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Does not affect function
DNA change (genomic) (Relative to hg38 / GRCh38) g.534242A>G
Reference -
DB-ID HRAS_000001
dbSNP ID -
Variant remarks -
Average frequency (gnomAD v.2.1.1) 0.3157 View details
Owner Lina Nuñez-Private Practice
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Instituto Nacional del Cancer
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Protein     

Zygosity     

Co_ocurrence     

RNA change     

Review status     
HRAS NM_005343.3 -/- 2 c.81T>C p.(His27=) Hetero no r.(?) -



Screenings


AscendingScreening ID     

Template     

Technique     

Lab     

Remarks     

Date of test     

Type of test     

Genes screened     

Variants found     

Owner     
0000001809 DNA CNV;SEQ-NG Invitae (deriv. Genesia) Invitae Multi-Cancer Panel (84 genes) 27-nov-2019 Multigenetic panel - 116 Lina Nuñez-Private Practice