chr7:140781602:C>A Detail (hg38) (BRAF)

Information

Genome

Assembly Position
hg19 chr7:140,481,402-140,481,402 View the variant detail on this assembly version.
hg38 chr7:140,781,602-140,781,602

HGVS

Type Transcript Protein
RefSeq NM_004333.4:c.1526G>T NP_004324.2:p.Gly509Val
Ensemble ENST00000288602.11:c.1526G>T ENST00000288602.11:p.Gly509Val
ENST00000496384.7:c.1406G>T ENST00000496384.7:p.Gly469Val
Summary

MGeND

Clinical significance
Variant entry
GWAS entry
Disease area statistics Show details

Frequency

[No Data.]

Prediction

ClinVar

Clinical Significance Pathogenic
Review star
Show details
Links
Type Database ID Link
Gene MIM 164757 OMIM
HGNC 1097 HGNC
Ensembl ENSG00000157764 Ensembl
NCBI NCBI
Gene Cards Gene Cards
OncoKB OncoKB
Type Database ID Link
Variant TogoVar
COSMIC COSM459 COSMIC
MONDO
Disease area statistics
[No Data.]
MGeND
[No Data.]
ClinVar
Clinical significance Last evaluated Review status Condition Origin Links
Pathogenic 2011-12-30 criteria provided, single submitter Non-small cell lung carcinoma somatic Detail
Likely pathogenic 2016-05-31 no assertion criteria provided multiple myeloma somatic Detail
Pathogenic 2014-10-02 no assertion criteria provided Neoplasm of the large intestine somatic Detail
Likely pathogenic 2016-05-31 no assertion criteria provided prostate adenocarcinoma somatic Detail
Likely pathogenic 2016-05-31 no assertion criteria provided lung adenocarcinoma somatic Detail
Likely pathogenic 2015-07-14 no assertion criteria provided Neoplasm somatic Detail
Likely pathogenic 2016-05-31 no assertion criteria provided somatic Detail
Likely pathogenic 2016-05-31 no assertion criteria provided somatic Detail
Likely pathogenic 2016-05-31 no assertion criteria provided Malignant melanoma of skin somatic Detail
Likely pathogenic 2016-05-31 no assertion criteria provided Squamous cell lung carcinoma somatic Detail
CIViC
[No Data.]
DisGeNET
Score Disease name Description Source Pubmed Links
0.242 Lymphoma, Non-Hodgkin NA CLINVAR Detail
0.567 Cardio-facio-cutaneous syndrome NA CLINVAR Detail
0.049 Metastatic melanoma Thus, the mutation BRAF G469A in MM might be related to a weak effectiveness of ... BeFree 26070258 Detail
0.015 Malignant neoplasm of lung The three most common BRAF mutations in lung cancers accounted for only 41% of t... BeFree 26386083 Detail
0.125 Carcinoma of lung The three most common BRAF mutations in lung cancers accounted for only 41% of t... BeFree 26386083 Detail
0.131 Non-small cell lung carcinoma NA CLINVAR Detail
Annotation

Annotations

DescrptionSourceLinks
NM_004333.6(BRAF):c.1406G>T (p.Gly469Val) AND Non-small cell lung carcinoma ClinVar Detail
NM_004333.6(BRAF):c.1406G>T (p.Gly469Val) AND Multiple myeloma ClinVar Detail
NM_004333.6(BRAF):c.1406G>T (p.Gly469Val) AND Neoplasm of the large intestine ClinVar Detail
NM_004333.6(BRAF):c.1406G>T (p.Gly469Val) AND Prostate adenocarcinoma ClinVar Detail
NM_004333.6(BRAF):c.1406G>T (p.Gly469Val) AND Lung adenocarcinoma ClinVar Detail
NM_004333.6(BRAF):c.1406G>T (p.Gly469Val) AND Neoplasm ClinVar Detail
NM_004333.6(BRAF):c.1406G>T (p.Gly469Val) AND Transitional cell carcinoma of the bladder ClinVar Detail
NM_004333.6(BRAF):c.1406G>T (p.Gly469Val) AND Squamous cell carcinoma of the skin ClinVar Detail
NM_004333.6(BRAF):c.1406G>T (p.Gly469Val) AND Malignant melanoma of skin ClinVar Detail
NM_004333.6(BRAF):c.1406G>T (p.Gly469Val) AND Squamous cell lung carcinoma ClinVar Detail
NA DisGeNET Detail
NA DisGeNET Detail
Thus, the mutation BRAF G469A in MM might be related to a weak effectiveness of therapy with BRAF in... DisGeNET Detail
The three most common BRAF mutations in lung cancers accounted for only 41% of the observed BRAF mut... DisGeNET Detail
The three most common BRAF mutations in lung cancers accounted for only 41% of the observed BRAF mut... DisGeNET Detail
NA DisGeNET Detail

Overlapped Transcript Coordinates

Gene Transcript ID Exon Number Chromosome Start Stop Type Amino Mutation Transcript Position Links

Overlapped Transcript

Gene Transcript ID Chromosome Start Stop Links
Gene
-
dbSNP
rs121913355 dbSNP
Genome
hg38
Position
chr7:140,781,602-140,781,602
Variant Type
snv
Reference Allele
C
Alternative Allele
A
Variant (CIViC) (CIViC Variant)
G469V
Transcript 1 (CIViC Variant)
ENST00000288602.6
Variant URL (CIViC Variant)
https://civic.genome.wustl.edu/links/variants/841
Genome browser