List of variants in gene CTC1 reported as likely benign for not specified

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 19

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HGVS	dbSNP	gnomAD frequency
NM_025099.6(CTC1):c.2458A>G (p.Ile820Val)	rs3027238	0.94552
NM_025099.6(CTC1):c.3013A>G (p.Ile1005Val)	rs3826543	0.77529
NM_025099.6(CTC1):c.990C>T (p.Asp330=)	rs74506939	0.15238
NM_025099.6(CTC1):c.1383G>A (p.Gln461=)	rs145192682	0.01148
NM_025099.6(CTC1):c.1720C>T (p.Pro574Ser)	rs200440641	0.00117
NM_025099.6(CTC1):c.147C>T (p.Val49=)	rs201492796	0.00114
NM_025099.6(CTC1):c.1728G>A (p.Pro576=)	rs78320653	0.00083
NM_025099.6(CTC1):c.189C>G (p.Leu63=)	rs188658691	0.00044
NM_025099.6(CTC1):c.1207-4C>T	rs369904656	0.00031
NM_025099.6(CTC1):c.1795C>T (p.Pro599Ser)	rs183556317	0.00029
NM_025099.6(CTC1):c.2895C>T (p.Ala965=)	rs373530008	0.00019
NM_025099.6(CTC1):c.597G>A (p.Thr199=)	rs373023392	0.00019
NM_025099.6(CTC1):c.1479A>G (p.Gln493=)	rs188654013	0.00018
NM_025099.6(CTC1):c.2472C>T (p.Pro824=)	rs558802130	0.00006
NM_025099.6(CTC1):c.258G>A (p.Ser86=)	rs369789111	0.00004
NM_025099.6(CTC1):c.3504C>T (p.Ile1168=)	rs760547081	0.00003
NM_025099.6(CTC1):c.105T>C (p.Asn35=)	rs775601506	0.00001
NM_025099.6(CTC1):c.1467C>T (p.His489=)	rs755429023	0.00001
NM_025099.6(CTC1):c.3276T>C (p.His1092=)

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