button p codon - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2540	NM_000243.3(MEFV):c.2177T>C (p.Val726Ala)	MEFV (V726A)	Single nucleotide variant (missense variant +1 more)	Familial Mediterranean fever +5 more	GPathogenic/Likely pathogenic
Select item 97467	NM_000243.3(MEFV):c.1894G>A (p.Gly632Ser)	LOC126862264, MEFV (G632S)	Single nucleotide variant (missense variant +1 more)	Acute febrile neutrophilic dermatosis +3 more	GConflicting classifications of pathogenicity
Select item 97545	NM_000243.3(MEFV):c.775A>G (p.Ile259Val)	MEFV (I259V)	Single nucleotide variant (missense variant +1 more)	Familial Mediterranean fever, autosomal dominant +6 more	GConflicting classifications of pathogenicity
Select item 2554	NM_000243.3(MEFV):c.443A>T (p.Glu148Val)	MEFV (E148V)	Single nucleotide variant (missense variant +1 more)	Acute febrile neutrophilic dermatosis +5 more	GConflicting classifications of pathogenicity
Select item 2542	NM_000243.3(MEFV):c.442G>C (p.Glu148Gln)	MEFV	Single nucleotide variant (missense variant +1 more)	Familial Mediterranean fever +7 more	GConflicting classifications of pathogenicity
Select item 97515	NM_000243.3(MEFV):c.322A>C (p.Ser108Arg)	MEFV (S108R)	Single nucleotide variant (missense variant +1 more)	not specified +6 more	GConflicting classifications of pathogenicity

ClinVar