Genomic variant #0000061747

Individual ID 00034559
Chromosome 1
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification -
DNA change (genomic) (Relative to hg19 / GRCh37) g.115258748C>A
DNA change (hg38) g.114716127C>A
Published as -
ISCN -
DB-ID NRAS_000003
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID -
Origin Somatic
Segregation -
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (large NGS studies) 1268 View details
Owner Phil Chambers
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NRAS NM_002524.4 ?/. 2 c.34G>T r.(?) p.(Gly12Cys)



Screenings


AscendingScreening ID     

Template     

Technique     

Tissue     

Remarks     

Genes screened     

Variants found     

Owner     
0000034630 DNA SEQ-NG-I - - NRAS 1 Phil Chambers