"ITMI"[submitter] AND "LOC130005443"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 134352	NM_022725.4(FANCF):c.1041G>T (p.Trp347Cys)	FANCF, LOC130005443 (W347C)	Single nucleotide variant (missense variant)	not specified	Gnot provided
Select item 134351	NM_022725.4(FANCF):c.959C>T (p.Pro320Leu)	FANCF, LOC130005443 (P320L)	Single nucleotide variant (missense variant)	not specified +3 more	GBenign/Likely benign
Select item 134350	NM_022725.4(FANCF):c.955C>T (p.Pro319Ser)	FANCF, LOC130005443 (P319S)	Single nucleotide variant (missense variant)	not specified	Gnot provided

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