"Ambry Genetics"[submitter] AND "LOC117038775"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3284674	NM_153633.3(HOXC4):c.14C>G (p.Ser5Trp)	HOXC4, LOC117038775 (S5W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2480085	NM_153633.3(HOXC4):c.77A>G (p.Asn26Ser)	HOXC4, LOC117038775 (N26S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2301657	NM_153633.3(HOXC4):c.83A>G (p.Tyr28Cys)	HOXC4, LOC117038775 (Y28C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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