List of variants in gene SDHA reported as not provided for nervous system cancer

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: 9

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HGVS	dbSNP	gnomAD frequency
NM_004168.4(SDHA):c.91C>T (p.Arg31Ter)	rs142441643	0.00025
NM_004168.4(SDHA):c.1055G>A (p.Arg352Gln)	rs199844384	0.00009
NM_004168.4(SDHA):c.313-7T>C	rs201972549	0.00004
NM_004168.4(SDHA):c.1652C>T (p.Thr551Met)	rs181238392	0.00002
NM_004168.4(SDHA):c.1679C>T (p.Thr560Met)	rs775350508	0.00002
NM_004168.4(SDHA):c.1099C>G (p.Gln367Glu)	rs780941330	0.00001
NM_004168.4(SDHA):c.1012del (p.Ala338fs)	rs1295239305
NM_004168.4(SDHA):c.245_252del (p.Glu82fs)	rs1734890180
NM_004168.4(SDHA):c.456+3_456+4delinsCT	rs1734966566

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