"ITMI"[submitter] AND "LOC126859807"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 135335	NM_001270508.2(TNFAIP3):c.619A>C (p.Ile207Leu)	LOC126859807, TNFAIP3 (I207L)	Single nucleotide variant (missense variant)	not provided +2 more	GBenign/Likely benign
Select item 135336	NM_001270508.2(TNFAIP3):c.742A>G (p.Ile248Val)	LOC126859807, TNFAIP3 (I248V)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance