List of variants in gene SUCLA2 reported as likely benign by PreventionGenetics, part of Exact Sciences

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_003850.3(SUCLA2):c.236C>T (p.Ser79Leu)	rs142289138	0.00062
NM_003850.3(SUCLA2):c.660C>T (p.Leu220=)	rs148794726	0.00051
NM_003850.3(SUCLA2):c.255A>G (p.Ala85=)	rs149108442	0.00048
NM_003850.3(SUCLA2):c.372-6T>C	rs139004670	0.00045
NM_003850.3(SUCLA2):c.1350G>A (p.Ala450=)	rs144969057	0.00036
NM_003850.3(SUCLA2):c.942C>T (p.Leu314=)	rs368442407	0.00017
NM_003850.3(SUCLA2):c.-3_-2del	rs570547911
NM_003850.3(SUCLA2):c.1002A>C (p.Ile334=)
NM_003850.3(SUCLA2):c.1011T>A (p.Leu337=)
NM_003850.3(SUCLA2):c.1017A>C (p.Gly339=)
NM_003850.3(SUCLA2):c.1020G>T (p.Gly340=)
NM_003850.3(SUCLA2):c.1029C>A (p.Ala343=)
NM_003850.3(SUCLA2):c.1108-9T>C
NM_003850.3(SUCLA2):c.225T>C (p.Tyr75=)
NM_003850.3(SUCLA2):c.900G>A (p.Arg300=)
NM_003850.3(SUCLA2):c.990C>A (p.Ala330=)
NM_003850.3(SUCLA2):c.993A>C (p.Thr331=)

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