"Labcorp Genetics (formerly Invitae), Labcorp"[submitter] AND "TLR5"[g - ClinVar - NCBI

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Items: 12

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 785793	NM_003268.6(TLR5):c.2493A>G (p.Lys831=)	TLR5	Single nucleotide variant (synonymous variant)	not provided	GBenign/Likely benign
Select item 791835	NM_003268.6(TLR5):c.2254A>G (p.Arg752Gly)	TLR5 (R752G)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 723575	NM_003268.6(TLR5):c.1661A>G (p.Asp554Gly)	TLR5 (D554G)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 723576	NM_003268.6(TLR5):c.1643C>T (p.Ala548Val)	TLR5 (A548V)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 252617	NM_003268.6(TLR5):c.1459C>A (p.Leu487Ile)	TLR5 (L487I)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign/Likely benign
Select item 780807	NM_003268.6(TLR5):c.1368T>C (p.Asn456=)	TLR5	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 775671	NM_003268.6(TLR5):c.1332C>T (p.Leu444=)	TLR5	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 709716	NM_003268.6(TLR5):c.867A>C (p.Ser289=)	TLR5	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 775672	NM_003268.6(TLR5):c.428A>C (p.Asn143Thr)	TLR5 (N143T)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 709717	NM_003268.6(TLR5):c.334C>G (p.Pro112Ala)	TLR5 (P112A)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 791521	NM_003268.6(TLR5):c.245C>T (p.Thr82Ile)	TLR5 (T82I)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 1003645	NC_000001.10:g.(?_130980840)_(248900000_?)dup	ARL8A, CNIH4 +956 more	Duplication	Gastrointestinal stromal tumor +2 more	GUncertain significance