"CeGaT Center for Human Genetics Tuebingen"[submitter] AND "ANLN"[gene - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1572693	NM_018685.5(ANLN):c.598G>A (p.Gly200Ser)	ANLN (G200S)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 3026006	NM_018685.5(ANLN):c.795C>T (p.Gly265=)	ANLN	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1014004	NM_018685.5(ANLN):c.1139G>A (p.Arg380His)	ANLN (R380H)	Single nucleotide variant (missense variant)	not provided	GConflicting classifications of pathogenicity
Select item 721054	NM_018685.5(ANLN):c.2193G>A (p.Gln731=)	ANLN	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 810084	NM_018685.5(ANLN):c.2476+4T>C	ANLN	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 720307	NM_018685.5(ANLN):c.2817C>T (p.Phe939=)	ANLN	Single nucleotide variant (synonymous variant)	ANLN-related condition +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)	not provided +2 more	GBenign/Likely benign

ClinVar