List of variants in gene TSEN54 reported as benign for not specified

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: 25

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HGVS	dbSNP	gnomAD frequency
NM_207346.3(TSEN54):c.1122G>C (p.Arg374=)	rs6501820	0.89534
NM_207346.3(TSEN54):c.285+32C>A	rs7218675	0.64612
NM_207346.3(TSEN54):c.1310C>T (p.Ala437Val)	rs8064529	0.63819
NM_207346.3(TSEN54):c.1041G>C (p.Lys347Asn)	rs9911502	0.58492
NM_207346.3(TSEN54):c.114T>G (p.His38Gln)	rs8079373	0.19277
NM_207346.3(TSEN54):c.285+3G>A	rs8074291	0.19227
NM_207346.3(TSEN54):c.333C>G (p.Arg111=)	rs6501818	0.19222
NM_207346.3(TSEN54):c.370-19C>A	rs56895494	0.12137
NM_207346.3(TSEN54):c.409A>C (p.Ile137Leu)	rs11559205	0.09934
NM_207346.3(TSEN54):c.1166A>C (p.Gln389Pro)	rs77247739	0.09564
NM_207346.3(TSEN54):c.521+39C>T	rs57636645	0.06538
NM_207346.3(TSEN54):c.624-37A>C	rs73998306	0.06523
NM_207346.3(TSEN54):c.1573G>C (p.Gly525Arg)	rs11870627	0.05898
NM_207346.3(TSEN54):c.1447C>G (p.Pro483Ala)	rs62088470	0.04801
NM_207346.3(TSEN54):c.568G>A (p.Val190Met)	rs79508780	0.04141
NM_207346.3(TSEN54):c.222-18C>T	rs113255333	0.02242
NM_207346.3(TSEN54):c.624-9G>A	rs138719855	0.01485
NM_207346.3(TSEN54):c.1468C>T (p.Arg490Trp)	rs144662042	0.01362
NM_207346.3(TSEN54):c.1328C>G (p.Ser443Cys)	rs150169668	0.01002
NM_207346.3(TSEN54):c.624-31A>G	rs191600766	0.00080
NM_207346.3(TSEN54):c.1368C>T (p.Asp456=)	rs138560086	0.00075
NM_207346.3(TSEN54):c.325C>G (p.Arg109Gly)	rs148146916	0.00053
NM_207346.3(TSEN54):c.1120C>G (p.Arg374Gly)	rs201351319
NM_207346.3(TSEN54):c.1120_1122delinsGGC (p.Arg374Gly)	rs1555644694
NM_207346.3(TSEN54):c.285+30GCCCTCCCT[2]	rs58038334

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