rs17695623

Variant names:

• chr7-140856757-C-A
• rs17695623
• NM_001374258.1:c.139-6545G>T

Variant summary

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

The NM_004333.6(BRAF):​c.139-6545G>T variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.0557 in 152,116 control chromosomes in the GnomAD database, including 279 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 0.056 (279 hom., cov: 32)
• Consequence: BRAF NM_004333.6 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -2.16

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=-1.01).
• BA1: GnomAd4 highest subpopulation (SAS) allele frequency at 95% confidence interval = 0.106 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
BRAF	NM_001374258.1	c.139-6545G>T		intron_variant	Intron 1 of 19	ENST00000644969.2	NP_001361187.1
BRAF	NM_004333.6	c.139-6545G>T		intron_variant	Intron 1 of 17	ENST00000646891.2	NP_004324.2

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
BRAF	ENST00000644969.2	c.139-6545G>T		intron_variant	Intron 1 of 19		NM_001374258.1	ENSP00000496776.1
BRAF	ENST00000646891.2	c.139-6545G>T		intron_variant	Intron 1 of 17		NM_004333.6	ENSP00000493543.1

Frequencies

GnomAD3 genomes AF: 0.0558 AC: 8477 AN: 151998 Hom.: 278 Cov.: 32

Gnomad AFR AF: 0.0222

Gnomad AMI AF: 0.0373

Gnomad AMR AF: 0.0530

Gnomad ASJ AF: 0.0735

Gnomad EAS AF: 0.0836

Gnomad SAS AF: 0.113

Gnomad FIN AF: 0.0584

Gnomad MID AF: 0.114

Gnomad NFE AF: 0.0692

Gnomad OTH AF: 0.0590

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

GnomAD4 genome AF: 0.0557 AC: 8476 AN: 152116 Hom.: 279 Cov.: 32 AF XY: 0.0565 AC XY: 4201 AN XY: 74366

Gnomad4 AFR AF: 0.0222

Gnomad4 AMR AF: 0.0529

Gnomad4 ASJ AF: 0.0735

Gnomad4 EAS AF: 0.0834

Gnomad4 SAS AF: 0.114

Gnomad4 FIN AF: 0.0584

Gnomad4 NFE AF: 0.0692

Gnomad4 OTH AF: 0.0583

Alfa AF: 0.0643 Hom.: 42

Bravo AF: 0.0522

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-1.0
CADD	Benign	0.076
DANN	Benign	0.75

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: rs17695623; hg19: chr7-140556557;