List of variants in gene FGF14 reported as likely benign 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
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 7

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HGVS	dbSNP	gnomAD frequency
NM_004115.4(FGF14):c.124G>T (p.Gly42Cys)	rs141304687	0.00191
NM_004115.4(FGF14):c.636T>C (p.His212=)	rs41281644	0.00149
NM_004115.4(FGF14):c.123C>T (p.Asn41=)	rs372705140	0.00033
NM_004115.4(FGF14):c.408+40847T>C
NM_004115.4(FGF14):c.408+40859G>C
NM_004115.4(FGF14):c.693G>T (p.Ala231=)	rs34397704
NM_004115.4(FGF14):c.88C>T (p.Arg30Trp)

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