"PreventionGenetics, part of Exact Sciences"[submitter] AND "SMG8"[gen - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2634400	NM_018149.7(SMG8):c.70G>A (p.Gly24Arg)	SMG8 (G24R)	Single nucleotide variant (missense variant)	SMG8-related disorder	GUncertain significance
Select item 3032972	NM_018149.7(SMG8):c.857C>G (p.Ala286Gly)	SMG8 (A286G)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GUncertain significance
Select item 3033024	NM_018149.7(SMG8):c.1057G>C (p.Asp353His)	SMG8 (D353H)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GUncertain significance
Select item 2633686	NM_018149.7(SMG8):c.1259T>C (p.Leu420Pro)	SMG8 (L420P)	Single nucleotide variant (missense variant)	SMG8-related disorder	GUncertain significance
Select item 3048743	NM_018149.7(SMG8):c.2209G>A (p.Val737Ile)	SMG8 (V737I)	Single nucleotide variant (missense variant)	SMG8-related disorder	GLikely benign
Select item 2632402	NM_018149.7(SMG8):c.2729T>G (p.Leu910Arg)	SMG8 (L910R)	Single nucleotide variant (missense variant)	SMG8-related disorder	GUncertain significance
Select item 2632723	NM_018149.7(SMG8):c.2779-10T>A	SMG8	Single nucleotide variant (intron variant)	SMG8-related disorder	GUncertain significance
Select item 3053941	NM_018149.7(SMG8):c.*1G>T	SMG8	Single nucleotide variant (3 prime UTR variant)	SMG8-related disorder	GLikely benign

ClinVar