"PreventionGenetics, part of Exact Sciences"[submitter] AND "TECTB"[ge - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3058168	NM_058222.3(TECTB):c.76+10C>T	TECTB	Single nucleotide variant (intron variant)	TECTB-related disorder	GLikely benign
Select item 3053331	NM_058222.3(TECTB):c.77-10C>T	TECTB	Single nucleotide variant (intron variant)	TECTB-related disorder	GLikely benign
Select item 3035636	NM_058222.3(TECTB):c.462A>G (p.Gln154=)	TECTB	Single nucleotide variant (synonymous variant)	TECTB-related disorder	GLikely benign
Select item 3035523	NM_058222.3(TECTB):c.463C>T (p.Leu155=)	TECTB	Single nucleotide variant (synonymous variant)	TECTB-related disorder	GLikely benign
Select item 3059723	NM_058222.3(TECTB):c.534C>G (p.Ser178=)	TECTB	Single nucleotide variant (synonymous variant)	TECTB-related disorder	GBenign
Select item 3049709	NM_058222.3(TECTB):c.627G>A (p.Ser209=)	TECTB	Single nucleotide variant (synonymous variant)	TECTB-related disorder	GLikely benign
Select item 3045814	NM_058222.3(TECTB):c.967T>C (p.Leu323=)	TECTB	Single nucleotide variant (synonymous variant)	TECTB-related disorder	GLikely benign

ClinVar