Related gene-specific medical variations for Gene (Select 7074) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3065611	NM_001353694.2(TIAM1):c.2357C>T (p.Thr786Ile)	TIAM1 (T761I +1 more)	Single nucleotide variant (missense variant)	Neurodevelopmental disorder with language delay and seizures	GUncertain significance
Select item 2685661	GRCh37/hg19 21q22.11(chr21:32528117-32806507)x1	TIAM1	Copy number loss	not provided	GUncertain significance
Select item 1809218	GRCh37/hg19 21q22.11(chr21:32736169-33013841)x1	TIAM1	Copy number loss	not provided	GUncertain significance
Select item 1807904	GRCh37/hg19 21q22.11(chr21:32472185-32600181)x1	TIAM1	Copy number loss	not provided	GUncertain significance
Select item 980233	GRCh37/hg19 21q22.11(chr21:32740461-32920742)x1	TIAM1	Copy number loss	not provided	GUncertain significance
Select item 816160	GRCh37/hg19 21q22.11(chr21:32586741-32840433)x1	TIAM1	Copy number loss	not provided	GUncertain significance
Select item 443576	GRCh37/hg19 21q22.11(chr21:32499143-32709435)x1	TIAM1	Copy number loss	See cases	GLikely benign

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