chr7:140481403:C>T Detail (hg19) (BRAF)

Information

Genome

Assembly Position
hg19 chr7:140,481,403-140,481,403
hg38 chr7:140,781,603-140,781,603 View the variant detail on this assembly version.

HGVS

Type Transcript Protein
RefSeq NM_004333.4:c.1525G>A NP_004324.2:p.Gly509Arg
Ensemble ENST00000288602.11:c.1525G>A ENST00000288602.11:p.Gly509Arg
ENST00000496384.7:c.1405G>A ENST00000496384.7:p.Gly469Arg
Summary

MGeND

Clinical significance not provided
Variant entry 1
GWAS entry
Disease area statistics Show details

Frequency

[No Data.]

Prediction

ClinVar

Clinical Significance Pathogenic Likely 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 COSM457 COSMIC
MONDO
Disease area statistics
MGeND
Clinical significance Last evaluated Condition Origin Submission ID Submitter Institute Citation Comment Image
not provided descending colon not provided MGS000041
(TMGS000094)
Hitoshi Nakagama National Cancer Center Japan
ClinVar
Clinical significance Last evaluated Review status Condition Origin Links
Likely pathogenic 2013-10-10 criteria provided, single submitter Non-small cell lung carcinoma somatic Detail
Likely pathogenic 2015-07-14 no assertion criteria provided melanoma somatic Detail
Pathogenic 2020-07-01 criteria provided, single submitter Noonan syndrome and Noonan-related syndrome germline Detail
CIViC
[No Data.]
DisGeNET
Score Disease name Description Source Pubmed Links
0.242 Lymphoma, Non-Hodgkin NA CLINVAR Detail
0.131 Non-small cell lung carcinoma We present a case report of a patient with NSCLC and the BRAF G469R mutation who... BeFree 26237499 Detail
0.131 Non-small cell lung carcinoma NA CLINVAR Detail
Annotation

Annotations

DescrptionSourceLinks
NM_004333.6(BRAF):c.1405G>A (p.Gly469Arg) AND Non-small cell lung carcinoma ClinVar Detail
NM_004333.6(BRAF):c.1405G>A (p.Gly469Arg) AND Melanoma ClinVar Detail
NM_004333.6(BRAF):c.1405G>A (p.Gly469Arg) AND Noonan syndrome and Noonan-related syndrome ClinVar Detail
NA DisGeNET Detail
We present a case report of a patient with NSCLC and the BRAF G469R mutation who showed a dramatic r... 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
rs121913357 dbSNP
Genome
hg19
Position
chr7:140,481,403-140,481,403
Variant Type
snv
Reference Allele
C
Alternative Allele
T
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