List of variants in gene BRAF reported as uncertain significance by Eurofins NTD LLC (GA)

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 8

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HGVS	dbSNP	gnomAD frequency
NM_004333.6(BRAF):c.138+17C>G	rs756400234	0.00002
NM_004333.6(BRAF):c.1518-9T>G	rs758498850	0.00002
NM_004333.6(BRAF):c.113C>T (p.Ala38Val)	rs886042293	0.00001
NM_004333.6(BRAF):c.1305G>A (p.Arg435=)	rs763771673	0.00001
NM_004333.6(BRAF):c.1317A>G (p.Lys439=)	rs569455230
NM_004333.6(BRAF):c.131C>T (p.Pro44Leu)	rs794726917
NM_004333.6(BRAF):c.83GCGCCG[4] (p.28GA[4])	rs397507458
NM_004333.6(BRAF):c.918C>G (p.Ser306=)	rs794727865

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