Variant #0000610874 (NC_000007.13:g.140624420_140624425dup, NM_004333.4:c.95_100dup (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.140624420_140624425dup
DNA change (hg38) g.140924620_140924625dup
Published as BRAF(NM_004333.4):c.100_101insGCGCCG (p.(Gly32_Ala33dup))
ISCN -
DB-ID BRAF_000073
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) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
BRAF NM_004333.4 -?/. - c.95_100dup r.(?) p.(Gly32_Ala33dup)


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