"Illumina Laboratory Services, Illumina"[submitter] AND "APOA2"[gene] - ClinVar - NCBI

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Items: 9

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 293291	NM_001643.2(APOA2):c.243G>A (p.Thr81=)	APOA2	Single nucleotide variant (synonymous variant)	Apolipoprotein A-II deficiency	GUncertain significance
Select item 876338	NM_001643.2(APOA2):c.229A>C (p.Lys77Gln)	APOA2 (K77Q)	Single nucleotide variant (missense variant)	Apolipoprotein A-II deficiency +1 more	GUncertain significance
Select item 293292	NM_001643.2(APOA2):c.186-4C>T	APOA2	Single nucleotide variant (intron variant)	APOA2-related condition +1 more	GBenign
Select item 874371	NM_001643.2(APOA2):c.121G>A (p.Val41Met)	APOA2 (V41M)	Single nucleotide variant (missense variant)	Apolipoprotein A-II deficiency +1 more	GUncertain significance
Select item 293293	NM_001643.2(APOA2):c.53-43TG[21]	APOA2	Microsatellite (intron variant)	not specified +2 more	GConflicting classifications of pathogenicity
Select item 293295	NM_001643.2(APOA2):c.53-43TG[16]	APOA2	Microsatellite (intron variant)	not specified +2 more	GConflicting classifications of pathogenicity
Select item 293294	NM_001643.2(APOA2):c.53-43TG[17]	APOA2	Microsatellite (intron variant)	not specified +2 more	GConflicting classifications of pathogenicity
Select item 293296	NM_001643.2(APOA2):c.-21G>A	APOA2	Single nucleotide variant (5 prime UTR variant)	Apolipoprotein A-II deficiency	GUncertain significance
Select item 293297	NM_001643.2(APOA2):c.-47C>T	APOA2	Single nucleotide variant (5 prime UTR variant)	Apolipoprotein A-II deficiency	GUncertain significance