"Labcorp Genetics (formerly Invitae), Labcorp"[submitter] AND "LOC1084 - ClinVar

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

Search results

Items: 25

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1778113	NM_001371904.1(APOA5):c.168G>C (p.Leu56=)	APOA5, LOC108491825	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 1187967	NM_001371904.1(APOA5):c.168G>A (p.Leu56=)	APOA5, LOC108491825	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype +1 more	GLikely benign
Select item 779436	NM_001371904.1(APOA5):c.165C>G (p.Thr55=)	APOA5, LOC108491825	Single nucleotide variant (synonymous variant)	not specified +2 more	GBenign/Likely benign
Select item 2023733	NM_001371904.1(APOA5):c.162-5T>A	APOA5, LOC108491825	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 2076102	NM_001371904.1(APOA5):c.162-8T>G	APOA5, LOC108491825	Single nucleotide variant (intron variant)	not provided +1 more	GBenign/Likely benign
Select item 1642388	NM_001371904.1(APOA5):c.161+19G>A	APOA5, LOC108491825	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2798990	NM_001371904.1(APOA5):c.161+15dup	APOA5, LOC108491825	Duplication (intron variant)	not provided	GBenign
Select item 1923334	NM_001371904.1(APOA5):c.161+14G>C	APOA5, LOC108491825	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1338538	NM_001371904.1(APOA5):c.161+5G>C	APOA5, LOC108491825	Single nucleotide variant (intron variant)	not provided +1 more	GUncertain significance
Select item 1776373	NM_001371904.1(APOA5):c.161+3G>A	APOA5, LOC108491825	Single nucleotide variant (intron variant)	not provided +1 more	GUncertain significance
Select item 1426712	NM_001371904.1(APOA5):c.153C>T (p.Arg51=)	APOA5, LOC108491825	Single nucleotide variant (synonymous variant)	not provided	GUncertain significance
Select item 1772233	NM_001371904.1(APOA5):c.141G>T (p.Gln47His)	APOA5, LOC108491825 (Q47H)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 496495	NM_001371904.1(APOA5):c.132C>A (p.Ile44=)	APOA5, LOC108491825	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign
Select item 2049432	NM_001371904.1(APOA5):c.119G>T (p.Arg40Met)	APOA5, LOC108491825 (R40M)	Single nucleotide variant (missense variant)	Cardiovascular phenotype +2 more	GConflicting classifications of pathogenicity
Select item 1428390	NM_001371904.1(APOA5):c.111del (p.Asp37fs)	APOA5, LOC108491825 (D37fs)	Deletion (frameshift variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 496494	NM_001371904.1(APOA5):c.111C>A (p.Asp37Glu)	APOA5, LOC108491825 (D37E)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign/Likely benign
Select item 1764008	NM_001371904.1(APOA5):c.85G>A (p.Asp29Asn)	LOC108491825, APOA5 (D29N)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 1604153	NM_001371904.1(APOA5):c.70C>A (p.Arg24=)	APOA5, LOC108491825	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype +1 more	GLikely benign
Select item 1749156	NM_001371904.1(APOA5):c.56C>T (p.Ser19Leu)	APOA5, LOC108491825 (S19L)	Single nucleotide variant (missense variant)	Cardiovascular phenotype +1 more	GUncertain significance
Select item 4403	NM_001371904.1(APOA5):c.56C>G (p.Ser19Trp)	APOA5, LOC108491825 (S19W)	Single nucleotide variant (missense variant)	not provided +4 more	GBenign/Likely benign
Select item 733372	NM_001371904.1(APOA5):c.50-9dup	APOA5, LOC108491825	Duplication (intron variant)	not provided	GLikely benign
Select item 1609167	NM_001371904.1(APOA5):c.49+10C>T	APOA5, LOC108491825	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2710449	NM_001371904.1(APOA5):c.49+5G>T	APOA5, LOC108491825	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 1965965	NM_001371904.1(APOA5):c.49+5G>A	APOA5, LOC108491825	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 2813598	NM_001371904.1(APOA5):c.43C>T (p.Leu15Phe)	APOA5, LOC108491825 (L15F)	Single nucleotide variant (missense variant)	not provided	GUncertain significance

ClinVar

Result Filters

Classification type

Germline classification

Types of conflicts

Molecular consequence

Variation type

Variation size

Variant length

Review status

Additional filters

Search results

Items: 25