"Labcorp Genetics (formerly Invitae), Labcorp"[submitter] AND "LOC1019 - ClinVar

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Search results

Items: 21

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 708992	NM_005357.4(LIPE):c.3172G>C (p.Gly1058Arg)	LOC101930071, LIPE +1 more (G1058R)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 795997	NM_005357.4(LIPE):c.3165C>T (p.Ala1055=)	LIPE, LIPE-AS1 +1 more	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 719524	NM_005357.4(LIPE):c.2880C>T (p.Tyr960=)	LIPE, LIPE-AS1 +1 more	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 778844	NM_005357.4(LIPE):c.2812C>A (p.Arg938Ser)	LIPE-AS1, LIPE +1 more (R938S)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 708271	NM_005357.4(LIPE):c.2662T>C (p.Ser888Pro)	LIPE, LIPE-AS1 +1 more (S888P)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 729455	NM_005357.4(LIPE):c.2655C>T (p.Ser885=)	LIPE, LIPE-AS1 +1 more	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 778845	NM_005357.4(LIPE):c.2262G>A (p.Pro754=)	LIPE, LIPE-AS1 +1 more	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 708902	NM_005357.4(LIPE):c.2224G>A (p.Gly742Arg)	LIPE, LIPE-AS1 +1 more (G742R)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign
Select item 790436	NM_005357.4(LIPE):c.2223C>T (p.Tyr741=)	LIPE, LIPE-AS1 +1 more	Single nucleotide variant (synonymous variant)	not specified +1 more	GBenign/Likely benign
Select item 731850	NM_005357.4(LIPE):c.1989C>T (p.His663=)	LIPE, LIPE-AS1 +1 more	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 736654	NM_005357.4(LIPE):c.1929G>A (p.Ser643=)	LIPE, LIPE-AS1 +1 more	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 778846	NM_005357.4(LIPE):c.1905G>A (p.Pro635=)	LIPE, LIPE-AS1 +1 more	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 738457	NM_005357.4(LIPE):c.1788A>G (p.Thr596=)	LIPE, LIPE-AS1 +1 more	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 784550	NM_005357.4(LIPE):c.1677G>A (p.Ser559=)	LIPE, LIPE-AS1 +1 more	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 708847	NM_005357.4(LIPE):c.1638C>T (p.Thr546=)	LIPE, LIPE-AS1 +1 more	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 723327	NM_005357.4(LIPE):c.1626C>T (p.Phe542=)	LIPE, LIPE-AS1 +1 more	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 737169	NM_005357.4(LIPE):c.1561G>A (p.Glu521Lys)	LIPE, LIPE-AS1 +1 more (E521K)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 728899	NM_005357.4(LIPE):c.1555G>A (p.Asp519Asn)	LIPE-AS1, LIPE +1 more (D519N)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign/Likely benign
Select item 797360	NM_005357.4(LIPE):c.1510+8C>T	LIPE, LIPE-AS1 +1 more	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 778601	NM_005357.4(LIPE):c.1495A>C (p.Asn499His)	LIPE, LIPE-AS1 +1 more (N499H)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 708000	NM_005357.4(LIPE):c.1491A>T (p.Lys497Asn)	LIPE, LIPE-AS1 +1 more (K497N)	Single nucleotide variant (missense variant)	not provided	GBenign/Likely benign

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Items: 21