ClinVar Miner

List of variants in gene FSCN2 reported by Eurofins NTD LLC (GA)

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Gene type:
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Total variants: 28
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HGVS dbSNP gnomAD frequency
NM_012418.4(FSCN2):c.738T>C (p.Pro246=) rs34567655 0.08398
NM_012418.4(FSCN2):c.1446C>T (p.Asp482=) rs143561119 0.04578
NM_012418.4(FSCN2):c.453C>T (p.Tyr151=) rs73367596 0.02072
NM_012418.4(FSCN2):c.381G>A (p.Pro127=) rs34454351 0.01717
NM_012418.4(FSCN2):c.333C>T (p.Phe111=) rs117946784 0.01608
NM_012418.4(FSCN2):c.309G>A (p.Arg103=) rs34126129 0.00952
NM_012418.4(FSCN2):c.732G>A (p.Thr244=) rs34797307 0.00864
NM_012418.4(FSCN2):c.412C>T (p.His138Tyr) rs143796236 0.00609
NM_012418.4(FSCN2):c.1106-6C>T rs11870517 0.00525
NM_012418.4(FSCN2):c.1425C>A (p.Gly475=) rs398123553 0.00488
NM_012418.4(FSCN2):c.150C>G (p.Pro50=) rs184519759 0.00391
NM_012418.4(FSCN2):c.1092C>T (p.Ile364=) rs188142101 0.00195
NM_012418.4(FSCN2):c.48C>T (p.Leu16=) rs199668780 0.00166
NM_012418.4(FSCN2):c.357C>T (p.Ser119=) rs189437871 0.00165
NM_012418.4(FSCN2):c.1230C>T (p.Asp410=) rs182593453 0.00148
NM_012418.4(FSCN2):c.492C>T (p.Asp164=) rs370382419 0.00080
NM_012418.4(FSCN2):c.984-7C>T rs139335460 0.00071
NM_012418.4(FSCN2):c.1274-3C>T rs201054437 0.00064
NM_012418.4(FSCN2):c.446G>A (p.Arg149Gln) rs181961770 0.00057
NM_012418.4(FSCN2):c.867C>T (p.His289=) rs368687488 0.00024
NM_012418.4(FSCN2):c.130C>T (p.Gln44Ter) rs200925863 0.00020
NM_012418.4(FSCN2):c.718G>A (p.Ala240Thr) rs370156011 0.00019
NM_012418.4(FSCN2):c.364G>A (p.Ala122Thr) rs782798108 0.00006
NM_012418.4(FSCN2):c.1277G>A (p.Arg426His) rs769242340 0.00005
NM_012418.4(FSCN2):c.349C>G (p.Gln117Glu) rs886044892 0.00004
NM_012418.4(FSCN2):c.*4C>T rs794727711 0.00003
NM_012418.4(FSCN2):c.1274-6C>T rs1048819854 0.00001
NM_012418.4(FSCN2):c.1312_1329del (p.Ser438_Gly443del) rs753094983

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