QTRT2[gene] and "single gene"[properties] - ClinVar - NCBI

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Items: 4

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2398719	NM_024638.4(QTRT2):c.113A>G (p.Lys38Arg)	QTRT2 (K38R +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2386673	NM_024638.4(QTRT2):c.700C>T (p.Arg234Cys)	QTRT2 (R111C +3 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2333876	NM_024638.4(QTRT2):c.1216T>A (p.Leu406Met)	QTRT2 (L300M +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2205711	NM_024638.4(QTRT2):c.1233C>G (p.His411Gln)	QTRT2 (H288Q +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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