7-140826083-C-T

Variant names:

• chr7-140826083-C-T
• rs1267610
• NM_001374258.1:c.504+8526G>A

Variant summary

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

The NM_004333.6(BRAF):​c.504+8526G>A 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 152,012 control chromosomes in the GnomAD database, including 18,081 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 (18081 hom., cov: 32)
• Consequence: BRAF NM_004333.6 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.521

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]

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.99).
• BA1: GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.819 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
BRAF	NM_001374258.1	c.504+8526G>A		intron_variant	Intron 3 of 19	ENST00000644969.2	NP_001361187.1
BRAF	NM_004333.6	c.504+8526G>A		intron_variant	Intron 3 of 17	ENST00000646891.2	NP_004324.2

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
BRAF	ENST00000644969.2	c.504+8526G>A		intron_variant	Intron 3 of 19		NM_001374258.1	ENSP00000496776.1
BRAF	ENST00000646891.2	c.504+8526G>A		intron_variant	Intron 3 of 17		NM_004333.6	ENSP00000493543.1

Frequencies

GnomAD3 genomes AF: 0.412 AC: 62511 AN: 151894 Hom.: 18014 Cov.: 32

Gnomad AFR AF: 0.826

Gnomad AMI AF: 0.206

Gnomad AMR AF: 0.307

Gnomad ASJ AF: 0.334

Gnomad EAS AF: 0.178

Gnomad SAS AF: 0.387

Gnomad FIN AF: 0.206

Gnomad MID AF: 0.434

Gnomad NFE AF: 0.242

Gnomad OTH AF: 0.389

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

GnomAD4 genome AF: 0.412 AC: 62628 AN: 152012 Hom.: 18081 Cov.: 32 AF XY: 0.407 AC XY: 30223 AN XY: 74308

Gnomad4 AFR AF: 0.826

Gnomad4 AMR AF: 0.307

Gnomad4 ASJ AF: 0.334

Gnomad4 EAS AF: 0.179

Gnomad4 SAS AF: 0.387

Gnomad4 FIN AF: 0.206

Gnomad4 NFE AF: 0.242

Gnomad4 OTH AF: 0.388

Alfa AF: 0.180 Hom.: 413

Bravo AF: 0.436

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.99
CADD	Benign	1.2
DANN	Benign	0.15
RBP_binding_hub_radar		0.0
RBP_regulation_power_radar		1.1

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: rs1267610; hg19: chr7-140525883;