List of variants in gene SMARCE1 reported as benign for central nervous system neoplasm

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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: 13

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HGVS	dbSNP	gnomAD frequency
NM_003079.5(SMARCE1):c.1231G>T (p.Glu411Ter)	rs62622817	0.00398
NM_003079.5(SMARCE1):c.369+12G>T	rs58739414	0.00232
NM_003079.5(SMARCE1):c.1101G>A (p.Lys367=)	rs148666451	0.00066
NM_003079.5(SMARCE1):c.1028-18A>G	rs202149619	0.00048
NM_003079.5(SMARCE1):c.351C>T (p.Asn117=)	rs149613910	0.00041
NM_003079.5(SMARCE1):c.894A>G (p.Lys298=)	rs759780963	0.00016
NM_003079.5(SMARCE1):c.369+10G>C	rs199790447	0.00012
NM_003079.5(SMARCE1):c.954C>T (p.Ile318=)	rs376628666	0.00005
NM_003079.5(SMARCE1):c.963G>A (p.Glu321=)	rs753203502	0.00005
NM_003079.5(SMARCE1):c.238-4dup
NM_003079.5(SMARCE1):c.541+14del	rs766497450
NM_003079.5(SMARCE1):c.817-15dup	rs747318581
NM_003079.5(SMARCE1):c.817-9del

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