List of variants in gene RAF1 reported as uncertain significance by Fulgent Genetics, Fulgent Genetics

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: 13

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HGVS	dbSNP	gnomAD frequency
NM_002880.4(RAF1):c.-209G>A	rs727504351	0.00035
NM_002880.4(RAF1):c.-181T>C	rs886057920	0.00022
NM_002880.4(RAF1):c.834+598G>A	rs375404697	0.00009
NM_002880.4(RAF1):c.-264C>G	rs894363344	0.00008
NM_002880.4(RAF1):c.1814C>T (p.Ser605Phe)	rs730881004	0.00006
NM_002880.4(RAF1):c.*643C>G	rs932173134	0.00004
NM_002880.4(RAF1):c.482A>G (p.Asn161Ser)	rs775781057	0.00001
NM_002880.4(RAF1):c.601A>G (p.Ile201Val)	rs757700986	0.00001
NM_002880.4(RAF1):c.-59C>G	rs201603517
NM_002880.4(RAF1):c.1463G>A (p.Gly488Asp)	rs865862568
NM_002880.4(RAF1):c.1770G>C (p.Lys590Asn)	rs773583951
NM_002880.4(RAF1):c.1867C>T (p.Pro623Ser)	rs373596121
NM_002880.4(RAF1):c.438C>A (p.Phe146Leu)	rs794727717

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