"Mayo Clinic Laboratories, Mayo Clinic"[submitter] AND "LOC100130987"[ - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1694057	NM_013246.3(CLCF1):c.392G>A (p.Arg131His)	CLCF1, LOC100130987 (R121H +1 more)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 3145390	NM_013246.3(CLCF1):c.389G>A (p.Arg130His)	CLCF1, LOC100130987 (R120H +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 1694058	NM_013246.3(CLCF1):c.164G>A (p.Arg55His)	CLCF1, LOC100130987 (R45H +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1694059	NM_013246.3(CLCF1):c.143G>A (p.Arg48His)	CLCF1, LOC100130987 (R38H +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1163927	NM_013246.3(CLCF1):c.112C>T (p.Pro38Ser)	CLCF1, LOC100130987 (P28S +1 more)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 1163928	NM_013246.3(CLCF1):c.89G>A (p.Arg30His)	CLCF1, LOC100130987 (R20H +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance

ClinVar