"Ambry Genetics"[submitter] AND "MFAP4"[gene] - ClinVar - NCBI

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Items: 17

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3125666	NM_002404.3(MFAP4):c.761G>A (p.Arg254Gln)	MFAP4 (R254Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2212017	NM_002404.3(MFAP4):c.569G>A (p.Arg190Gln)	MFAP4 (R214Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2322435	NM_002404.3(MFAP4):c.565G>A (p.Asp189Asn)	MFAP4 (D189N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2604738	NM_002404.3(MFAP4):c.466G>A (p.Ala156Thr)	MFAP4 (A180T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2272672	NM_002404.3(MFAP4):c.412A>T (p.Asn138Tyr)	MFAP4 (N162Y +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2605749	NM_002404.3(MFAP4):c.404T>C (p.Phe135Ser)	MFAP4 (F135S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2410508	NM_002404.3(MFAP4):c.229G>A (p.Gly77Arg)	MFAP4 (G77R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2606824	NM_002404.3(MFAP4):c.217A>C (p.Thr73Pro)	MFAP4 (T97P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2239759	NM_002404.3(MFAP4):c.70G>A (p.Gly24Arg)	MFAP4 (G24R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2458140	NM_002404.3(MFAP4):c.26T>C (p.Leu9Pro)	MFAP4 (L33P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2349750	NM_002404.3(MFAP4):c.17C>G (p.Ala6Gly)	MFAP4 (A30G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3125665	NM_002404.3(MFAP4):c.6+103G>C	MFAP4 (L24F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2557055	NM_002404.3(MFAP4):c.6+102T>C	MFAP4 (L24S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2360052	NM_002404.3(MFAP4):c.6+93G>T	MFAP4 (G21V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3125664	NM_002404.3(MFAP4):c.6+75G>A	MFAP4 (G15D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2531635	NM_002404.3(MFAP4):c.6+50C>T	MFAP4 (L7F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2340917	NM_002404.3(MFAP4):c.6+41C>G	MFAP4 (L4V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance