List of variants in gene FGF14 reported as uncertain significance by Athena Diagnostics Inc

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: 10

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HGVS	dbSNP	gnomAD frequency
NM_004115.4(FGF14):c.256C>A (p.His86Asn)	rs758950207	0.00001
NM_175929.3(FGF14):c.142A>T (p.Ser48Cys)	rs756852215	0.00001
NM_004115.4(FGF14):c.126C>T (p.Gly42=)
NM_004115.4(FGF14):c.154C>T (p.Arg52Cys)
NM_004115.4(FGF14):c.304+5G>A
NM_004115.4(FGF14):c.311T>C (p.Phe104Ser)	rs1555301921
NM_004115.4(FGF14):c.369G>C (p.Leu123Phe)	rs746040831
NM_004115.4(FGF14):c.552G>C (p.Gly184=)	rs1204741145
NM_175929.3(FGF14):c.177C>T (p.Gly59=)
NM_175929.3(FGF14):c.46T>A (p.Leu16Ile)	rs773941026

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