Related gene-specific medical variations for Gene (Select 27067) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3323200	NM_001164380.2(STAU2):c.1599C>G (p.Ile533Met)	STAU2, STAU2-AS1 (I467M +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3171147	NM_001164380.2(STAU2):c.1663C>T (p.Pro555Ser)	STAU2, STAU2-AS1 (P489S +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3171146	NM_001164380.2(STAU2):c.1538T>C (p.Leu513Ser)	STAU2, STAU2-AS1 (L447S +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2616086	NM_001164380.2(STAU2):c.1678G>A (p.Ala560Thr)	STAU2, STAU2-AS1 (A388T +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2590662	NM_001164380.2(STAU2):c.1607G>T (p.Gly536Val)	STAU2, STAU2-AS1 (G536V +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2339376	NM_001164380.2(STAU2):c.1675A>G (p.Ile559Val)	STAU2, STAU2-AS1 (I493V +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1690318	NM_001164380.2(STAU2):c.226C>T (p.Pro76Ser)	STAU2 (P38S +2 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 979239	GRCh37/hg19 8q21.11(chr8:74275902-74626066)x3	STAU2	Copy number gain	not provided	GUncertain significance

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