Related gene-specific medical variations for Gene (Select 22839) - ClinVar - NCBI

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Items: 9

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3082863	NM_001365621.2(DLGAP4):c.2749G>C (p.Glu917Gln)	DLGAP4, DLGAP4-AS1 (E210Q +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2652299	NM_001365621.2(DLGAP4):c.2814G>A (p.Pro938=)	DLGAP4, DLGAP4-AS1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2540047	NM_001365621.2(DLGAP4):c.2785G>T (p.Val929Phe)	DLGAP4, DLGAP4-AS1 (V929F +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2524571	NM_001365621.2(DLGAP4):c.2783C>T (p.Pro928Leu)	DLGAP4, DLGAP4-AS1 (P234L +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2470017	NM_001365621.2(DLGAP4):c.2833G>A (p.Ala945Thr)	DLGAP4, DLGAP4-AS1 (A238T +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2225813	NM_001365621.2(DLGAP4):c.2779C>A (p.Pro927Thr)	DLGAP4, DLGAP4-AS1 (P233T +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2207694	NM_001365621.2(DLGAP4):c.2824C>T (p.Arg942Cys)	DLGAP4, DLGAP4-AS1 (R235C +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 769088	NM_001365621.2(DLGAP4):c.2535T>C (p.Ala845=)	DLGAP4, DLGAP4-AS1	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 753648	NM_001365621.2(DLGAP4):c.2778C>T (p.Pro926=)	DLGAP4, DLGAP4-AS1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign