7-140828517-A-G

Position:

• chr7-140828517-A-G

Variant summary

Our verdict is Benign. Variant got -12 ACMG points: 0P and 12B. BP4_Strong BA1

The NM_004333.6(BRAF):​c.504+6092T>C variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.412 in 152,078 control chromosomes in the GnomAD database, including 18,135 homozygotes. In-silico tool predicts a benign outcome for this variant. No clinical diagnostic laboratories have submitted clinical-significance assessments for this variant to ClinVar.

• Frequency: Genomes: 𝑓 0.41 (18135 hom., cov: 32)
• Consequence: BRAF NM_004333.6 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.0620

Genes affected

BRAF (HGNC:1097): (B-Raf proto-oncogene, serine/threonine kinase) This gene encodes a protein belonging to the RAF family of serine/threonine protein kinases. This protein plays a role in regulating the MAP kinase/ERK signaling pathway, which affects cell division, differentiation, and secretion. Mutations in this gene, most commonly the V600E mutation, are the most frequently identified cancer-causing mutations in melanoma, and have been identified in various other cancers as well, including non-Hodgkin lymphoma, colorectal cancer, thyroid carcinoma, non-small cell lung carcinoma, hairy cell leukemia and adenocarcinoma of lung. Mutations in this gene are also associated with cardiofaciocutaneous, Noonan, and Costello syndromes, which exhibit overlapping phenotypes. A pseudogene of this gene has been identified on the X chromosome. [provided by RefSeq, Aug 2017]

BRAF (HGNC:):

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-1.01).
• BA1: GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.82 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	Protein	UniProt
BRAF	NM_001374258.1	c.504+6092T>C		intron_variant		ENST00000644969.2	NP_001361187.1
BRAF	NM_004333.6	c.504+6092T>C		intron_variant		ENST00000646891.2	NP_004324.2

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Protein	Appris	UniProt
BRAF	ENST00000644969.2	c.504+6092T>C		intron_variant			NM_001374258.1	ENSP00000496776.1
BRAF	ENST00000646891.2	c.504+6092T>C		intron_variant			NM_004333.6	ENSP00000493543.1

Frequencies

GnomAD3 genomes AF: 0.412 AC: 62617 AN: 151962 Hom.: 18069 Cov.: 32

Gnomad AFR AF: 0.827

Gnomad AMI AF: 0.206

Gnomad AMR AF: 0.309

Gnomad ASJ AF: 0.334

Gnomad EAS AF: 0.179

Gnomad SAS AF: 0.388

Gnomad FIN AF: 0.205

Gnomad MID AF: 0.434

Gnomad NFE AF: 0.242

Gnomad OTH AF: 0.390

We have no GnomAD4 exomes data on this position. Probably position not covered by the project.

GnomAD4 genome AF: 0.412 AC: 62732 AN: 152078 Hom.: 18135 Cov.: 32 AF XY: 0.407 AC XY: 30269 AN XY: 74342

Gnomad4 AFR AF: 0.827

Gnomad4 AMR AF: 0.308

Gnomad4 ASJ AF: 0.334

Gnomad4 EAS AF: 0.180

Gnomad4 SAS AF: 0.388

Gnomad4 FIN AF: 0.205

Gnomad4 NFE AF: 0.242

Gnomad4 OTH AF: 0.389

Alfa AF: 0.288 Hom.: 3524

Bravo AF: 0.435

Asia WGS AF: 0.326 AC: 1134 AN: 3476

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-1.0
CADD	Benign	2.3
DANN	Benign	0.56

Splicing

Name	Calibrated prediction	Score	Prediction
SpliceAI score (max)		0.0		Details are displayed if max score is > 0.2

Find out detailed SpliceAI scores and Pangolin per-transcript scores at spliceailookup.broadinstitute.org

Publications

LitVar

Other links and lift over

dbSNP: rs1267622; hg19: chr7-140528317;