List of variants in gene FGF14 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: 16

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_001321940.1(FGF14):c.2T>C (p.Met1Thr)	rs61965280	0.00943
NM_004115.4(FGF14):c.*1259C>T	rs535930764	0.00357
NM_004115.4(FGF14):c.*414T>C	rs557390242	0.00200
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.1220_1223dup	rs546246953	0.00062
NM_004115.4(FGF14):c.123C>T (p.Asn41=)	rs372705140	0.00033
NM_004115.4(FGF14):c.351G>A (p.Gln117=)	rs1555301901	0.00001
NM_004115.4(FGF14):c.919_922dup	rs768342824
NM_004115.4(FGF14):c.352G>A (p.Gly118Arg)	rs779936498
NM_004115.4(FGF14):c.408+40847T>C
NM_004115.4(FGF14):c.408+40859G>C
NM_004115.4(FGF14):c.423del (p.Glu142fs)
NM_004115.4(FGF14):c.439G>T (p.Glu147Ter)	rs865878627
NM_004115.4(FGF14):c.520G>A (p.Gly174Arg)	rs1594043304
NM_004115.4(FGF14):c.693G>T (p.Ala231=)	rs34397704

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.