Related gene-specific medical variations for Gene (Select 7099) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2613884	NM_138554.5(TLR4):c.22G>T (p.Ala8Ser)	LOC126860749, TLR4 (A8S)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2431158	NM_138554.5(TLR4):c.6G>T (p.Met2Ile)	LOC126860749, TLR4 (M2I)	Single nucleotide variant (5 prime UTR variant +1 more)	Lung adenocarcinoma	GUncertain significance
Select item 2409803	NM_138554.5(TLR4):c.61G>A (p.Val21Met)	LOC126860749, TLR4 (V21M)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2354214	NM_138554.5(TLR4):c.64A>G (p.Arg22Gly)	LOC126860749, TLR4 (R22G)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 1809467	GRCh37/hg19 9q33.1(chr9:120197413-120521544)x3	TLR4	Copy number gain	not provided	GUncertain significance
Select item 100604	NM_138554.5(TLR4):c.842G>A (p.Cys281Tyr)	TLR4 (C281Y +2 more)	Single nucleotide variant (missense variant)	not provided	Gnot provided

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