ARRDC3[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 2387656	NM_020801.4(ARRDC3):c.1241G>A (p.Arg414His)	ARRDC3 (R194H +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3316328	NM_020801.4(ARRDC3):c.1240C>T (p.Arg414Cys)	ARRDC3 (R194C +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2476253	NM_020801.4(ARRDC3):c.1201C>G (p.Pro401Ala)	ARRDC3 (P181A +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2401628	NM_020801.4(ARRDC3):c.1189A>G (p.Ile397Val)	ARRDC3 (I177V +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3316317	NM_020801.4(ARRDC3):c.1147A>G (p.Ile383Val)	ARRDC3 (I163V +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3129858	NM_020801.4(ARRDC3):c.1037C>T (p.Pro346Leu)	ARRDC3 (P126L +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 92008	NM_020801.4(ARRDC3):c.1022A>G (p.Glu341Gly)	ARRDC3 (E341G +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 746406	NM_020801.4(ARRDC3):c.837C>T (p.Asp279=)	ARRDC3	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2233973	NM_020801.4(ARRDC3):c.737T>C (p.Leu246Pro)	ARRDC3 (L246P +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2304897	NM_020801.4(ARRDC3):c.679G>A (p.Ala227Thr)	ARRDC3 (A7T +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3129859	NM_020801.4(ARRDC3):c.608C>A (p.Thr203Asn)	ARRDC3 (T203N)	Single nucleotide variant (5 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 2616658	NM_020801.4(ARRDC3):c.560C>T (p.Thr187Ile)	ARRDC3 (T187I)	Single nucleotide variant (5 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 768019	NM_020801.4(ARRDC3):c.453A>G (p.Lys151=)	ARRDC3	Single nucleotide variant (5 prime UTR variant +3 more)	not provided	GBenign
Select item 2552260	NM_020801.4(ARRDC3):c.433C>T (p.Pro145Ser)	ARRDC3 (P145S)	Single nucleotide variant (5 prime UTR variant +3 more)	not specified	GUncertain significance
Select item 2342446	NM_020801.4(ARRDC3):c.404G>A (p.Arg135His)	ARRDC3 (R135H)	Single nucleotide variant (5 prime UTR variant +3 more)	not specified	GUncertain significance
Select item 3316306	NM_020801.4(ARRDC3):c.325A>G (p.Arg109Gly)	ARRDC3 (R109G)	Single nucleotide variant (5 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 2387612	NM_020801.4(ARRDC3):c.311C>T (p.Thr104Ile)	ARRDC3 (T104I)	Single nucleotide variant (5 prime UTR variant +2 more)	not specified	GUncertain significance