"Invitae"[submitter] AND "TESC"[gene] - ClinVar - NCBI

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Items: 11

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 720006	NM_017899.4(TESC):c.609C>T (p.Arg203=)	TESC	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 731115	NM_017899.4(TESC):c.603C>T (p.His201=)	TESC	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 768589	NM_017899.4(TESC):c.502G>A (p.Val168Met)	TESC (V141M +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GBenign
Select item 742597	NM_017899.4(TESC):c.495G>A (p.Ala165=)	TESC	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 787934	NM_017899.4(TESC):c.447C>T (p.Ile149=)	TESC	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 756914	NM_017899.4(TESC):c.432G>A (p.Ser144=)	TESC	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 731885	NM_017899.4(TESC):c.381C>T (p.Asp127=)	TESC	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 791322	NM_017899.4(TESC):c.350-9C>A	TESC	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 715914	NM_017899.4(TESC):c.297C>T (p.Asp99=)	TESC	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 745672	NM_017899.4(TESC):c.249C>A (p.Ile83=)	TESC	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 735733	NM_017899.4(TESC):c.195C>T (p.Ala65=)	TESC	Single nucleotide variant (synonymous variant +2 more)	not provided	GLikely benign