Variant #0000254418 (NC_000001.10:g.115258746A>C, NRAS(NM_002524.4):c.36T>G)

Chromosome 1
Allele Unknown
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.115258746A>C
DNA change (hg38) g.114716125A>C
Published as NRAS(NM_002524.3):c.36T>G (p.G12=)
ISCN -
DB-ID NRAS_000018
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (large NGS studies) Variant not found in online data sets
Owner VKGL-NL_Rotterdam
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NRAS NM_002524.4 -?/. - c.36T>G r.(?) p.(Gly12=)
CSDE1 NM_007158.5 -?/. - c.*2044T>G r.(=) p.(=)