"Fulgent Genetics, Fulgent Genetics"[submitter] AND "ANLN"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 599127	NM_018685.5(ANLN):c.31C>T (p.Arg11Ter)	ANLN (R11*)	Single nucleotide variant (nonsense)	not provided +1 more	GUncertain significance
Select item 1612035	NM_018685.5(ANLN):c.173-16A>G	ANLN	Single nucleotide variant (intron variant)	not provided +1 more	GBenign/Likely benign
Select item 1524609	NM_018685.5(ANLN):c.1127G>A (p.Arg376His)	ANLN (R376H)	Single nucleotide variant (missense variant)	not specified +2 more	GUncertain significance
Select item 960990	NM_018685.5(ANLN):c.1171C>T (p.Arg391Cys)	ANLN (R391C)	Single nucleotide variant (missense variant)	Focal segmental glomerulosclerosis 8 +1 more	GUncertain significance
Select item 1170048	NM_018685.5(ANLN):c.1686G>A (p.Ser562=)	ANLN	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign/Likely benign
Select item 1026642	NM_018685.5(ANLN):c.2440A>G (p.Lys814Glu)	ANLN (K776E +2 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 1168523	NM_018685.5(ANLN):c.2971-12T>G	ANLN	Single nucleotide variant (intron variant)	not provided +1 more	GBenign/Likely benign
Select item 1154941	NM_018685.5(ANLN):c.3325A>G (p.Ile1109Val)	ANLN (I1071V +2 more)	Single nucleotide variant (missense variant)	Focal segmental glomerulosclerosis 8 +1 more	GBenign/Likely benign

ClinVar