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

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 769973	NM_152657.4(GGN):c.1939C>T (p.Gln647Ter)	GGN (Q647*)	Single nucleotide variant (nonsense)	GGN-related condition +1 more	GBenign/Likely benign
Select item 3026019	NM_152657.4(GGN):c.1334_1345del (p.441PPPT[1])	GGN	Deletion (inframe_deletion)	not provided	GUncertain significance
Select item 769453	NM_152657.4(GGN):c.1177C>T (p.Pro393Ser)	GGN (P393S)	Single nucleotide variant (missense variant)	not provided	GBenign/Likely benign
Select item 774957	NM_152657.4(GGN):c.1104G>A (p.Gly368=)	GGN	Single nucleotide variant (synonymous variant)	not provided	GBenign/Likely benign
Select item 775410	NM_152657.4(GGN):c.593C>T (p.Pro198Leu)	GGN (P198L)	Single nucleotide variant (missense variant)	not provided	GBenign/Likely benign
Select item 2649789	NM_152657.4(GGN):c.492T>C (p.Phe164=)	GGN	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3026402	NM_152657.4(GGN):c.362G>A (p.Arg121Gln)	GGN (R121Q)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2649790	NM_152657.4(GGN):c.147C>T (p.Val49=)	GGN	Single nucleotide variant (synonymous variant)	not provided	GLikely benign

ClinVar