"Ambry Genetics"[submitter] AND "LOC101928540"[gene] - ClinVar - NCBI

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Items: 8

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3278889	NM_015687.5(FILIP1):c.242T>A (p.Ile81Asn)	FILIP1, LOC101928540 (I81N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3278886	NM_015687.5(FILIP1):c.200G>C (p.Arg67Pro)	FILIP1, LOC101928540 (R70P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2370935	NM_015687.5(FILIP1):c.169C>G (p.Arg57Gly)	FILIP1, LOC101928540 (R57G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2340539	NM_015687.5(FILIP1):c.164T>A (p.Val55Asp)	FILIP1, LOC101928540 (V55D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2283060	NM_015687.5(FILIP1):c.157G>C (p.Gly53Arg)	FILIP1, LOC101928540 (G53R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2404437	NM_015687.5(FILIP1):c.131G>A (p.Arg44Lys)	FILIP1, LOC101928540 (R47K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3095234	NM_015687.5(FILIP1):c.73G>A (p.Gly25Ser)	FILIP1, LOC101928540 (G25S +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2537175	NM_015687.5(FILIP1):c.31G>A (p.Ala11Thr)	FILIP1, LOC101928540 (A11T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance