List of variants in gene BRAF reported as benign for RASopathy

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 33

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HGVS	dbSNP	gnomAD frequency
NM_004333.6(BRAF):c.1929A>G (p.Gly643=)	rs9648696	0.30796
NM_004333.6(BRAF):c.-19C>T	rs71645935	0.01115
NM_004333.6(BRAF):c.78G>T (p.Glu26Asp)	rs371877084	0.01088
NM_004333.6(BRAF):c.1315-18T>G	rs6959000	0.00840
NM_004333.6(BRAF):c.1383A>G (p.Gln461=)	rs56216404	0.00399
NM_004333.6(BRAF):c.1141-19C>T	rs71645959	0.00360
NM_004333.6(BRAF):c.1227A>G (p.Ser409=)	rs145035762	0.00318
NM_004333.6(BRAF):c.1517+20T>C	rs71645980	0.00273
NM_004333.6(BRAF):c.1433-19A>G	rs369635503	0.00114
NM_004333.6(BRAF):c.1332G>A (p.Arg444=)	rs56101602	0.00068
NM_004333.6(BRAF):c.2127+3A>G	rs371976102	0.00043
NM_004333.6(BRAF):c.2235A>G (p.Leu745=)	rs56046546	0.00030
NM_004333.6(BRAF):c.64G>A (p.Asp22Asn)	rs397507456	0.00025
NM_004333.6(BRAF):c.504+17A>G	rs201797624	0.00013
NM_004333.6(BRAF):c.968C>T (p.Ser323Leu)	rs397516907	0.00012
NM_004333.6(BRAF):c.36G>A (p.Ala12=)	rs397507454	0.00011
NM_004333.6(BRAF):c.375T>G (p.Ser125=)	rs201507202	0.00008
NM_004333.6(BRAF):c.-18C>G	rs397507453	0.00006
NM_004333.6(BRAF):c.504+19C>T	rs780617193	0.00006
NM_004333.6(BRAF):c.1150A>G (p.Arg384Gly)	rs545495379	0.00004
NM_004333.6(BRAF):c.1694+14G>A	rs184144181	0.00003
NM_004333.6(BRAF):c.708C>T (p.Asn236=)	rs138333692	0.00003
NM_004333.6(BRAF):c.712-18T>C	rs535496777	0.00001
NM_004333.6(BRAF):c.976A>G (p.Ile326Val)	rs775040765	0.00001
NM_004333.6(BRAF):c.1178-12dup
NM_004333.6(BRAF):c.1992+16G>A	rs3789806
NM_004333.6(BRAF):c.1992+16G>C	rs3789806
NM_004333.6(BRAF):c.1993-10dup
NM_004333.6(BRAF):c.1993-11del	rs759069424
NM_004333.6(BRAF):c.1993-11dup	rs759069424
NM_004333.6(BRAF):c.2128-26dup	rs370332827
NM_004333.6(BRAF):c.2128-5del	rs373442098
NM_004333.6(BRAF):c.2128-5dup	rs373442098

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