"Ambry Genetics"[submitter] AND "GJD3-AS1"[gene] - ClinVar - NCBI

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Items: 16

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2228756	NM_152219.4(GJD3):c.823G>A (p.Glu275Lys)	GJD3, GJD3-AS1 +1 more (E275K)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2495239	NM_152219.4(GJD3):c.718C>T (p.Pro240Ser)	GJD3, GJD3-AS1 +1 more (P240S)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2397274	NM_152219.4(GJD3):c.701C>T (p.Ala234Val)	GJD3, GJD3-AS1 +1 more (A234V)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2249060	NM_152219.4(GJD3):c.685C>A (p.Arg229Ser)	GJD3, GJD3-AS1 +1 more (R229S)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2620777	NM_152219.4(GJD3):c.632A>G (p.His211Arg)	GJD3, GJD3-AS1 +1 more (H211R)	Single nucleotide variant (non-coding transcript variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2274113	NM_152219.4(GJD3):c.536G>T (p.Cys179Phe)	GJD3, GJD3-AS1 (C179F)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2594831	NM_152219.4(GJD3):c.491C>T (p.Pro164Leu)	GJD3, GJD3-AS1 (P164L)	Single nucleotide variant (non-coding transcript variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2376796	NM_152219.4(GJD3):c.439G>A (p.Glu147Lys)	GJD3, GJD3-AS1 (E147K)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2278785	NM_152219.4(GJD3):c.391C>T (p.Arg131Cys)	GJD3-AS1, GJD3 (R131C)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2372732	NM_152219.4(GJD3):c.289A>T (p.Met97Leu)	GJD3, GJD3-AS1 (M97L)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2287545	NM_152219.4(GJD3):c.266C>G (p.Pro89Arg)	GJD3, GJD3-AS1 (P89R)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2238555	NM_152219.4(GJD3):c.230T>C (p.Phe77Ser)	GJD3, GJD3-AS1 (F77S)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2473340	NM_152219.4(GJD3):c.221A>C (p.His74Pro)	GJD3, GJD3-AS1 (H74P)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2281668	NM_152219.4(GJD3):c.161G>C (p.Cys54Ser)	GJD3, GJD3-AS1 (C54S)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2557334	NM_152219.4(GJD3):c.157G>C (p.Val53Leu)	GJD3, GJD3-AS1 (V53L)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2332771	NM_152219.4(GJD3):c.97C>T (p.Arg33Cys)	GJD3, GJD3-AS1 (R33C)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance