Variants in gene RAF1 with conflicting interpretations "likely pathogenic" and "pathogenic"

Submission 1 (likely pathogenic) minimum review status:		Submission 1 (likely pathogenic) method:
Submission 2 (pathogenic) minimum review status:		Submission 2 (pathogenic) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 15

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HGVS	dbSNP	gnomAD frequency
NM_002880.4(RAF1):c.1082G>C (p.Gly361Ala)	rs397516813
NM_002880.4(RAF1):c.1472C>T (p.Thr491Ile)	rs80338799
NM_002880.4(RAF1):c.1837C>G (p.Leu613Val)	rs80338797
NM_002880.4(RAF1):c.524A>G (p.His175Arg)	rs397516822
NM_002880.4(RAF1):c.770C>T (p.Ser257Leu)	rs80338796
NM_002880.4(RAF1):c.775T>A (p.Ser259Thr)	rs3730271
NM_002880.4(RAF1):c.775T>C (p.Ser259Pro)	rs3730271
NM_002880.4(RAF1):c.776C>G (p.Ser259Cys)	rs397516827
NM_002880.4(RAF1):c.779C>T (p.Thr260Ile)	rs869025501
NM_002880.4(RAF1):c.781C>G (p.Pro261Ala)	rs121434594
NM_002880.4(RAF1):c.781C>T (p.Pro261Ser)	rs121434594
NM_002880.4(RAF1):c.782C>G (p.Pro261Arg)	rs397516828
NM_002880.4(RAF1):c.782C>T (p.Pro261Leu)	rs397516828
NM_002880.4(RAF1):c.788T>C (p.Val263Ala)	rs397516830
NM_002880.4(RAF1):c.788T>G (p.Val263Gly)	rs397516830

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