List of variants in gene NT5C2 reported as benign for complex hereditary spastic paraplegia

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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: 8

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HGVS	dbSNP	gnomAD frequency
NM_001351169.2(NT5C2):c.7A>G (p.Thr3Ala)	rs10883841	0.10846
NM_001351169.2(NT5C2):c.1211+20C>A	rs17094683	0.08793
NM_001351169.2(NT5C2):c.921+18T>G	rs17115449	0.00452
NM_001351169.2(NT5C2):c.1077A>G (p.Lys359=)	rs141391492	0.00083
NM_001351169.2(NT5C2):c.634-14T>G	rs200522283	0.00022
NM_001351169.2(NT5C2):c.540-4G>A	rs201261415	0.00019
NM_001351169.2(NT5C2):c.634-13dup
NM_001351169.2(NT5C2):c.772-5del

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