chr7:140801503:G>T Detail (hg38) (BRAF)

Information

Genome

Assembly Position
hg19 chr7:140,501,303-140,501,303 View the variant detail on this assembly version.
hg38 chr7:140,801,503-140,801,503

HGVS

Type Transcript Protein
RefSeq NM_004333.4:c.769C>A NP_004324.2:p.Gln257Lys
Ensemble ENST00000288602.11:c.769C>A ENST00000288602.11:p.Gln257Lys
ENST00000496384.7:c.769C>A ENST00000496384.7:p.Gln257Lys
Summary

MGeND

Clinical significance Pathogenic
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 COSM6005619 COSMIC
MONDO
Disease area statistics
MGeND
Clinical significance Last evaluated Condition Origin Submission ID Submitter Institute Citation Comment Image
Pathogenic 2017/03/30 cardiofaciocutaneous syndrome germline MGS000001
(TMGS000137) 		Kenjiro Kosaki Keio University
ClinVar
Clinical significance Last evaluated Review status Condition Origin Links
Likely pathogenic 2015-01-02 criteria provided, single submitter Cardio-facio-cutaneous syndrome,Noonan syndrome germline Detail
Likely pathogenic 2015-01-02 criteria provided, single submitter Cardio-facio-cutaneous syndrome,Noonan syndrome germline Detail
Pathogenic 2013-05-07 criteria provided, single submitter not provided germline Detail
Likely pathogenic 2017-10-11 criteria provided, single submitter Inborn genetic diseases germline Detail
Pathogenic 2023-03-08 criteria provided, single submitter RASopathy germline Detail
CIViC
[No Data.]
DisGeNET
Score Disease name Description Source Pubmed Links
0.567 Cardio-facio-cutaneous syndrome NA CLINVAR Detail
Annotation

Annotations

DescrptionSourceLinks
NM_004333.6(BRAF):c.769C>A (p.Gln257Lys) AND multiple conditions ClinVar Detail
NM_004333.6(BRAF):c.769C>A (p.Gln257Lys) AND multiple conditions ClinVar Detail
NM_004333.6(BRAF):c.769C>A (p.Gln257Lys) AND not provided ClinVar Detail
NM_004333.6(BRAF):c.769C>A (p.Gln257Lys) AND Inborn genetic diseases ClinVar Detail
NM_004333.6(BRAF):c.769C>A (p.Gln257Lys) AND RASopathy ClinVar 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
rs397507469 dbSNP
Genome
hg38
Position
chr7:140,801,503-140,801,503
Variant Type
snv
Reference Allele
G
Alternative Allele
T
Genome browser