ClinVar Miner

List of variants in gene FGF14 reported by Athena Diagnostics Inc

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Gene type:
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Total variants: 22
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HGVS dbSNP gnomAD frequency
NM_004115.4(FGF14):c.481T>C (p.Leu161=) rs77082831 0.01311
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.373A>G (p.Ile125Val) rs34073982 0.00135
NM_004115.4(FGF14):c.579A>T (p.Ala193=) rs138607344 0.00044
NM_004115.4(FGF14):c.123C>T (p.Asn41=) rs372705140 0.00033
NM_004115.4(FGF14):c.153G>A (p.Val51=) rs148687898 0.00028
NM_004115.4(FGF14):c.564G>A (p.Lys188=) rs556509693 0.00004
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_175929.3(FGF14):c.69C>T (p.Leu23=) rs775136913 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_004115.4(FGF14):c.564del (p.Thr190fs) rs2035456443
NM_004115.4(FGF14):c.608-9del rs558457368
NM_004115.4(FGF14):c.693G>A (p.Ala231=) rs34397704
NM_175929.3(FGF14):c.177C>T (p.Gly59=)
NM_175929.3(FGF14):c.46T>A (p.Leu16Ile) rs773941026

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