Variant #0000502580 (NC_000001.10:g.115256530G>T, NRAS(NM_002524.4):c.181C>A)

Chromosome 1
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.115256530G>T
DNA change (hg38) g.114713909G>T
Published as NRAS(NM_002524.3):c.181C>A (p.Q61K)
ISCN -
DB-ID NRAS_000002 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 -
Methylation -
Average frequency (large NGS studies) Variant not found in online data sets
Owner VKGL-NL_AMC
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NRAS NM_002524.4 +/. - c.181C>A r.(?) p.(Gln61Lys)
CSDE1 NM_007158.5 +/. - c.*4260C>A r.(=) p.(=)