Variant #0000604676 (NC_000001.10:g.115258748C>T, NRAS(NM_002524.4):c.34G>A)

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.115258748C>T
DNA change (hg38) g.114716127C>T
Published as -
ISCN -
DB-ID NRAS_000005 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_Nijmegen
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NRAS NM_002524.4 +?/. - c.34G>A r.(?) p.(Gly12Ser)
CSDE1 NM_007158.5 +?/. - c.*2042G>A r.(=) p.(=)