Variant #0000300432 (NC_000001.10:g.115252280C>T, NRAS(NM_002524.4):c.360G>A)

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.115252280C>T
DNA change (hg38) g.114709659C>T
Published as NRAS(NM_002524.3):c.360G>A (p.L120=)
ISCN -
DB-ID NRAS_000015 See all 2 reported entries
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) 0.00038 View details
Owner VKGL-NL_Utrecht
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NRAS NM_002524.4 -?/. - c.360G>A r.(?) p.(Leu120=)