"PreventionGenetics, part of Exact Sciences"[submitter] AND "TRIM36"[g - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 721327	NM_001300759.2(TRIM36):c.2137C>G (p.Gln713Glu)	TRIM36 (Q713E +2 more)	Single nucleotide variant (missense variant)	TRIM36-related disorder +1 more	GBenign
Select item 3060721	NM_001300759.2(TRIM36):c.1331A>G (p.Asn444Ser)	TRIM36 (N301S +2 more)	Single nucleotide variant (missense variant)	TRIM36-related disorder	GBenign
Select item 3059952	NM_001300759.2(TRIM36):c.1211-7C>T	TRIM36	Single nucleotide variant (intron variant)	TRIM36-related disorder	GBenign
Select item 3034195	NM_001300759.2(TRIM36):c.745T>A (p.Ser249Thr)	TRIM36 (S106T +2 more)	Single nucleotide variant (missense variant)	TRIM36-related disorder	GLikely benign
Select item 3060373	NM_001300759.2(TRIM36):c.666G>A (p.Leu222=)	TRIM36	Single nucleotide variant (synonymous variant)	TRIM36-related disorder	GBenign
Select item 3037329	NM_001300759.2(TRIM36):c.582A>G (p.Arg194=)	TRIM36	Single nucleotide variant (synonymous variant)	TRIM36-related disorder	GLikely benign
Select item 3039400	NM_001300759.2(TRIM36):c.372C>G (p.Phe124Leu)	TRIM36 (F124L +1 more)	Single nucleotide variant (5 prime UTR variant +1 more)	TRIM36-related disorder	GLikely benign
Select item 3038086	NM_001017397.2(TRIM36):c.78A>G (p.Arg26=)	TRIM36	Single nucleotide variant (synonymous variant +1 more)	TRIM36-related disorder	GBenign

ClinVar