Variant #0000258696 (NC_000007.13:g.140624426C>A, BRAF(NM_004333.4):c.78G>T)

Chromosome 7
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.140624426C>A
DNA change (hg38) g.140924626C>A
Published as BRAF(NM_004333.4):c.78G>T (p.E26D)
ISCN -
DB-ID BRAF_000019 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) 0.00494 View details
Owner VKGL-NL_AMC
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
BRAF NM_004333.4 -/. - c.78G>T r.(?) p.(Glu26Asp)