Variant #0000345689 (NC_000001.10:g.115258747C>A, NRAS(NM_002524.4):c.35G>T)

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.115258747C>A
DNA change (hg38) g.114716126C>A
Published as -
ISCN -
DB-ID NRAS_000006 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) 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.35G>T r.(?) p.(Gly12Val)
CSDE1 NM_007158.5 +/. - c.*2043G>T r.(=) p.(=)