"CeGaT Center for Human Genetics Tuebingen"[submitter] AND "ATP11C"[ge - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2661532	NM_001353812.2(ATP11C):c.3357A>G (p.Leu1119=)	ATP11C	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2661533	NM_001353812.2(ATP11C):c.2871A>G (p.Leu957=)	ATP11C	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2661534	NM_001353812.2(ATP11C):c.762C>T (p.Thr254=)	ATP11C	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2661535	NM_001353812.2(ATP11C):c.585A>G (p.Ala195=)	ATP11C	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2266203	NM_001353812.2(ATP11C):c.559C>A (p.His187Asn)	ATP11C (H187N +1 more)	Single nucleotide variant (missense variant)	ATP11C-related condition +2 more	GConflicting classifications of pathogenicity
Select item 2661536	NM_001353812.2(ATP11C):c.90G>A (p.Ser30=)	ATP11C	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2661537	NM_001353812.2(ATP11C):c.28-5335C>T	ATP11C (S11F)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 3024654	GRCh37/hg19 Xq12-28(chrX:67292994-155240074)x3	ALG13, AMMECR1 +488 more	Copy number gain	not provided	GPathogenic

ClinVar