REXO4[gene] and "single gene"[properties] - ClinVar - NCBI

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Items: 17

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2409733	NM_020385.4(REXO4):c.1223G>T (p.Arg408Met)	REXO4 (R236M +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2377463	NM_020385.4(REXO4):c.1217G>A (p.Arg406Gln)	REXO4 (R269Q +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3313835	NM_020385.4(REXO4):c.1214C>T (p.Ala405Val)	REXO4 (A268V +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3153312	NM_020385.4(REXO4):c.1195A>G (p.Lys399Glu)	REXO4 (K227E +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2380354	NM_020385.4(REXO4):c.1183G>A (p.Val395Ile)	REXO4 (V223I +3 more)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GLikely benign
Select item 3153311	NM_020385.4(REXO4):c.1163A>C (p.Gln388Pro)	REXO4 (Q388P +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2550614	NM_020385.4(REXO4):c.1156G>A (p.Asp386Asn)	REXO4 (D386N +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3153310	NM_020385.4(REXO4):c.1153C>G (p.Gln385Glu)	REXO4 (Q385E +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3153309	NM_020385.4(REXO4):c.1049A>G (p.Tyr350Cys)	REXO4 (Y178C +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2508877	NM_020385.4(REXO4):c.890G>A (p.Arg297Gln)	REXO4 (R297Q +2 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2204366	NM_020385.4(REXO4):c.889C>T (p.Arg297Trp)	REXO4 (R160W +2 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3153320	NM_020385.4(REXO4):c.875C>T (p.Ala292Val)	REXO4 (A155V +2 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3153319	NM_020385.4(REXO4):c.850G>A (p.Glu284Lys)	REXO4 (E284K +2 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3153318	NM_020385.4(REXO4):c.826T>C (p.Tyr276His)	REXO4 (Y183H +2 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2361681	NM_020385.4(REXO4):c.667A>G (p.Ser223Gly)	REXO4 (S223G +2 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 812699	NM_020385.4(REXO4):c.664C>T (p.Gln222Ter)	REXO4 (Q129* +2 more)	Single nucleotide variant (nonsense +2 more)	not provided	GUncertain significance
Select item 3153317	NM_020385.4(REXO4):c.573G>A (p.Glu191=)	REXO4	Single nucleotide variant (synonymous variant +2 more)	not specified	GLikely benign