chr7:140477861:T>G Detail (hg19) (BRAF)

Information

Genome

Assembly Position
hg19 chr7:140,477,861-140,477,861
hg38 chr7:140,778,061-140,778,061 View the variant detail on this assembly version.

HGVS

Type Transcript Protein
RefSeq NM_004333.4:c.1567A>C NP_004324.2:p.Lys523Gln
Ensemble ENST00000496384.7:c.1447A>C ENST00000496384.7:p.Lys483Gln
ENST00000288602.11:c.1567A>C ENST00000288602.11:p.Lys523Gln
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
MONDO
Disease area statistics
MGeND
Clinical significance Last evaluated Condition Origin Submission ID Submitter Institute Citation Comment Image
not provided bronchus or lung, unspecified not provided MGS000042
(TMGS000093) 		Hitoshi Nakagama National Cancer Center Japan
ClinVar
Clinical significance Last evaluated Review status Condition Origin Links
Likely pathogenic 2014-04-02 criteria provided, single submitter Cardio-facio-cutaneous syndrome germline unknown Detail
Pathogenic 2023-11-13 criteria provided, single submitter not provided 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.1447A>C (p.Lys483Gln) AND Cardio-facio-cutaneous syndrome ClinVar Detail
NM_004333.6(BRAF):c.1447A>C (p.Lys483Gln) AND not provided 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
rs397507474 dbSNP
Genome
hg19
Position
chr7:140,477,861-140,477,861
Variant Type
snv
Reference Allele
T
Alternative Allele
G
Genome browser