List of variants reported as likely benign for cardiofaciocutaneous syndrome 1 by Fulgent Genetics, Fulgent Genetics

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Total variants: 24

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HGVS	dbSNP	gnomAD frequency
NM_004333.6(BRAF):c.1141-19C>T	rs71645959	0.00360
NM_004333.6(BRAF):c.981-20C>T	rs374896031	0.00066
NM_004333.6(BRAF):c.2127+3A>G	rs371976102	0.00043
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.1993-11T>C	rs750297886	0.00009
NM_004333.6(BRAF):c.399A>G (p.Ser133=)	rs397507463	0.00009
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.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.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

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