List of variants in gene TSEN34 reported as benign for central nervous system malformation

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: 17

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HGVS	dbSNP	gnomAD frequency
NM_001077446.4(TSEN34):c.795= (p.Pro265=)	rs7595	0.80164
NM_001077446.4(TSEN34):c.*497=	rs36621	0.80151
NM_001077446.4(TSEN34):c.*928A>G	rs144441443	0.02975
NM_001077446.4(TSEN34):c.*1128G>T	rs79447697	0.02881
NM_001077446.4(TSEN34):c.*29G>A	rs2289145	0.02347
NM_001077446.4(TSEN34):c.688C>A (p.Arg230=)	rs11879943	0.02345
NM_001077446.4(TSEN34):c.*688T>A	rs115025822	0.01302
NM_001077446.4(TSEN34):c.*815G>A	rs36620	0.00944
NM_001077446.4(TSEN34):c.*175T>C	rs77548142	0.00549
NM_001077446.4(TSEN34):c.334C>G (p.Leu112Val)	rs17849378	0.00493
NM_001077446.4(TSEN34):c.*109A>G	rs181231588	0.00482
NM_001077446.4(TSEN34):c.39G>A (p.Val13=)	rs184898622	0.00426
NM_001077446.4(TSEN34):c.*865A>G	rs187570218	0.00272
NM_001077446.4(TSEN34):c.*1163C>G	rs115093373
NM_001077446.4(TSEN34):c.*245A>C	rs4042
NM_001077446.4(TSEN34):c.*385=	rs1156850349
NM_001077446.4(TSEN34):c.*385A>C	rs36622

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