"Revvity Omics, Revvity"[submitter] AND "TNRC6B"[gene] - ClinVar - NCBI

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Items: 7

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2437162	NM_001162501.2(TNRC6B):c.157G>A (p.Ala53Thr)	TNRC6B (A53T +1 more)	Single nucleotide variant (missense variant)	Global developmental delay with speech and behavioral abnormalities	GUncertain significance
Select item 2437164	NM_001162501.2(TNRC6B):c.1111G>A (p.Asp371Asn)	TNRC6B (D371N)	Single nucleotide variant (missense variant +1 more)	Global developmental delay with speech and behavioral abnormalities	GUncertain significance
Select item 2437161	NM_001162501.2(TNRC6B):c.1268G>T (p.Gly423Val)	TNRC6B (G423V)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 2437159	NM_001162501.2(TNRC6B):c.2420A>C (p.Asn807Thr)	TNRC6B (N807T)	Single nucleotide variant (missense variant +1 more)	Global developmental delay with speech and behavioral abnormalities	GUncertain significance
Select item 2690250	NM_001162501.2(TNRC6B):c.2888G>T (p.Gly963Val)	TNRC6B (G216V +1 more)	Single nucleotide variant (missense variant +1 more)	Global developmental delay with speech and behavioral abnormalities	GUncertain significance
Select item 2437160	NM_001162501.2(TNRC6B):c.2927G>A (p.Gly976Glu)	TNRC6B (G229E +1 more)	Single nucleotide variant (missense variant +1 more)	Global developmental delay with speech and behavioral abnormalities	GUncertain significance
Select item 2437163	NM_001162501.2(TNRC6B):c.4592C>G (p.Ser1531Cys)	TNRC6B (S1421C +2 more)	Single nucleotide variant (missense variant)	Global developmental delay with speech and behavioral abnormalities	GUncertain significance