Variant #0000531000 (NC_000007.13:g.140494246C>T, BRAF(NM_004333.4):c.1002G>A)

Chromosome 7
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.140494246C>T
DNA change (hg38) g.140794446C>T
Published as BRAF(NM_004333.4):c.1002G>A (p.P334=)
ISCN -
DB-ID BRAF_000061
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_Rotterdam
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
BRAF NM_004333.4 -?/. - c.1002G>A r.(?) p.(Pro334=)