Genomic variant #0000346651

Chromosome 1
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.115258711A>T
DNA change (hg38) -
Published as -
ISCN -
DB-ID NRAS_000007 See all 5 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)     

ClassClinical     

RNA change     

Protein     
NRAS NM_002524.4 +/. - c.71T>A pathogenic r.(?) p.(Ile24Asn)
CSDE1 NM_007158.5 +/. - c.*2079T>A pathogenic r.(=) p.(=)