Variant #0000163496 (NC_000001.10:g.115256532C>T, NRAS(NM_002524.4):c.179G>A)

Individual ID 00100630
Chromosome 1
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.115256532C>T
DNA change (hg38) g.114713911C>T
Published as -
ISCN -
DB-ID NRAS_000010 See all 5 reported entries
Variant remarks -
Reference Altmüller et al, submitted
ClinVar ID -
dbSNP ID -
Origin Germline
Segregation yes
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (large NGS studies) Variant not found in online data sets
Owner Christina Lissewski
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NRAS NM_002524.4 +?/. 3 c.179G>A r.(?) p.(Gly60Glu)



Screenings


AscendingScreening ID     

Template     

Technique     

Tissue     

Remarks     

Genes screened     

Variants found     

Owner     
0000101046 DNA SEQ - - NRAS 1 Christina Lissewski