List of variants in gene RAF1 reported as uncertain significance by Eurofins NTD LLC (GA)

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: 10

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HGVS	dbSNP	gnomAD frequency
NM_002880.4(RAF1):c.122G>A (p.Arg41Gln)	rs145611571	0.00016
NM_002880.4(RAF1):c.1668+4A>G	rs771344560	0.00002
NM_002880.4(RAF1):c.639T>C (p.Thr213=)	rs397516823	0.00002
NM_002880.4(RAF1):c.683C>G (p.Ser228Cys)	rs766437069	0.00001
NM_002880.4(RAF1):c.1178A>C (p.Glu393Ala)	rs886042569
NM_002880.4(RAF1):c.121C>T (p.Arg41Trp)	rs1480507957
NM_002880.4(RAF1):c.124_125delinsAT (p.Ala42Ile)	rs876657965
NM_002880.4(RAF1):c.321-13dup	rs2125421223
NM_002880.4(RAF1):c.325_327del (p.Lys109del)	rs1418886913
NM_002880.4(RAF1):c.438C>A (p.Phe146Leu)	rs794727717

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