List of variants in gene BRAF reported as likely benign for immune system disorder

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: 36

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HGVS	dbSNP	gnomAD frequency
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.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.2127+3A>G	rs371976102	0.00043
NM_004333.6(BRAF):c.2235A>G (p.Leu745=)	rs56046546	0.00030
NM_004333.6(BRAF):c.-5A>G	rs71645936	0.00024
NM_004333.6(BRAF):c.240+18A>G	rs368584855	0.00017
NM_004333.6(BRAF):c.1860+16A>G	rs368859030	0.00016
NM_004333.6(BRAF):c.36G>A (p.Ala12=)	rs397507454	0.00011
NM_004333.6(BRAF):c.1993-11T>C	rs750297886	0.00009
NM_004333.6(BRAF):c.399A>G (p.Ser133=)	rs397507463	0.00009
NM_004333.6(BRAF):c.375T>G (p.Ser125=)	rs201507202	0.00008
NM_004333.6(BRAF):c.1694+13C>T	rs368578780	0.00007
NM_004333.6(BRAF):c.504+19C>T	rs780617193	0.00006
NM_004333.6(BRAF):c.915G>A (p.Ala305=)	rs145675911	0.00004
NM_004333.6(BRAF):c.1314+17T>C	rs1057524397	0.00003
NM_004333.6(BRAF):c.2128-10_2128-9insC	rs758588300	0.00003
NM_004333.6(BRAF):c.2136C>T (p.Ala712=)	rs377165711	0.00003
NM_004333.6(BRAF):c.1433-18G>A	rs763267814	0.00002
NM_004333.6(BRAF):c.101C>T (p.Ala34Val)	rs1424449802	0.00001
NM_004333.6(BRAF):c.1338G>A (p.Ser446=)	rs765215499	0.00001
NM_004333.6(BRAF):c.1848C>A (p.Ser616=)	rs752115982	0.00001
NM_004333.6(BRAF):c.1992+15C>T	rs766089848	0.00001
NM_004333.6(BRAF):c.298T>C (p.Leu100=)	rs761709697	0.00001
NM_004333.6(BRAF):c.712-18T>C	rs535496777	0.00001
NM_004333.6(BRAF):c.*111C>T	rs539860876
NM_004333.6(BRAF):c.1206C>A (p.Pro402=)	rs201758035
NM_004333.6(BRAF):c.1432+17_1432+19del	rs777363183
NM_004333.6(BRAF):c.1719C>A (p.Ile573=)	rs2128999629
NM_004333.6(BRAF):c.1992+16G>C	rs3789806
NM_004333.6(BRAF):c.2128-27_2128-19del	rs761539834
NM_004333.6(BRAF):c.2128-5del	rs373442098
NM_004333.6(BRAF):c.83GCGCCG[1] (p.28GA[1])	rs397507458
NM_004333.6(BRAF):c.83GCGCCG[4] (p.28GA[4])	rs397507458

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