Variant #0000263742 (NC_000007.13:g.140482908T>C, NM_004333.4:c.1227A>G (BRAF))

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.140482908T>C
DNA change (hg38) g.140783108T>C
Published as BRAF(NM_004333.4):c.1227A>G (p.S409=), BRAF(NM_004333.6):c.1227A>G (p.S409=)
ISCN -
DB-ID BRAF_000043 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 (gnomAD v.2.1.1) 0.00319 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-04-16 21:50:28 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
BRAF NM_004333.4 -?/. - c.1227A>G r.(?) p.(Ser409=)


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