"Ambry Genetics"[submitter] AND "LOC130004089"[gene] - ClinVar

Warning: The NCBI web site requires JavaScript to function. more...

Format

Sort by

Choose Destination

Search results

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3280184	NM_173540.3(FUT11):c.454A>G (p.Asn152Asp)	FUT11, LOC130004089 (N152D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3097473	NM_173540.3(FUT11):c.499C>G (p.Leu167Val)	FUT11, LOC130004089 (L167V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance