List of variants in gene GGN reported by CeGaT Center for Human Genetics Tuebingen

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 8

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HGVS	dbSNP	gnomAD frequency
NM_152657.4(GGN):c.593C>T (p.Pro198Leu)	rs183879202	0.00792
NM_152657.4(GGN):c.1177C>T (p.Pro393Ser)	rs202082712	0.00462
NM_152657.4(GGN):c.1104G>A (p.Gly368=)	rs148446446	0.00073
NM_152657.4(GGN):c.1334_1345del (p.441PPPT[1])
NM_152657.4(GGN):c.147C>T (p.Val49=)
NM_152657.4(GGN):c.1939C>T (p.Gln647Ter)	rs62123481
NM_152657.4(GGN):c.362G>A (p.Arg121Gln)
NM_152657.4(GGN):c.492T>C (p.Phe164=)

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