List of variants in gene BRAF reported as likely benign by Women's Health and Genetics/Laboratory Corporation of America, LabCorp

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: 19

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HGVS	dbSNP	gnomAD frequency
NM_004333.6(BRAF):c.1141-12A>G	rs375704079	0.00014
NM_004333.6(BRAF):c.1433-5T>C	rs587780861	0.00006
NM_004333.6(BRAF):c.1667T>C (p.Ile556Thr)	rs760524720	0.00004
NM_004333.6(BRAF):c.622A>G (p.Ile208Val)	rs727504571	0.00003
NM_004333.6(BRAF):c.193T>C (p.Leu65=)	rs866875749	0.00001
NM_004333.6(BRAF):c.2082A>G (p.Ala694=)	rs375174370	0.00001
NM_004333.6(BRAF):c.2229T>C (p.Phe743=)	rs397516901	0.00001
NM_004333.6(BRAF):c.750T>C (p.Phe250=)	rs754568893	0.00001
NM_004333.6(BRAF):c.111G>A (p.Ser37=)	rs727502906
NM_004333.6(BRAF):c.1206C>T (p.Pro402=)	rs201758035
NM_004333.6(BRAF):c.1245C>T (p.Ala415=)
NM_004333.6(BRAF):c.2064C>T (p.Ala688=)	rs1554389847
NM_004333.6(BRAF):c.2128-16_2128-15delinsTC	rs2130870208
NM_004333.6(BRAF):c.213G>A (p.Glu71=)
NM_004333.6(BRAF):c.279A>G (p.Gln93=)	rs150050723
NM_004333.6(BRAF):c.612G>A (p.Glu204=)	rs1202874043
NM_004333.6(BRAF):c.669T>C (p.His223=)	rs2129047893
NM_004333.6(BRAF):c.83GCGCCG[2] (p.28GA[2])	rs397507458
NM_004333.6(BRAF):c.83GCGCCG[4] (p.28GA[4])	rs397507458

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