"PreventionGenetics, part of Exact Sciences"[submitter] AND "RARB"[gen - ClinVar - NCBI

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Items: 9

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2629886	NM_001290216.3(RARB):c.130del (p.Leu44fs)	RARB (L44fs)	Deletion (frameshift variant)	RARB-related disorder	GUncertain significance
Select item 2632393	NM_001290216.3(RARB):c.130C>G (p.Leu44Val)	RARB (L44V)	Single nucleotide variant (missense variant)	RARB-related disorder	GUncertain significance
Select item 772966	NM_000965.5(RARB):c.270G>A (p.Gly90=)	RARB	Single nucleotide variant (synonymous variant +2 more)	RARB-related disorder +1 more	GBenign
Select item 713568	NM_000965.5(RARB):c.696C>T (p.Ile232=)	RARB	Single nucleotide variant (synonymous variant +1 more)	not provided +1 more	GLikely benign
Select item 3037092	NM_000965.5(RARB):c.702G>C (p.Glu234Asp)	RARB (E122D +4 more)	Single nucleotide variant (missense variant +1 more)	RARB-related disorder	GUncertain significance
Select item 1600081	NM_000965.5(RARB):c.920A>C (p.Asn307Thr)	RARB (N195T +4 more)	Single nucleotide variant (missense variant +2 more)	RARB-related disorder +1 more	GBenign
Select item 474675	NM_000965.5(RARB):c.1155A>G (p.Ala385=)	RARB	Single nucleotide variant (synonymous variant +1 more)	RARB-related disorder +2 more	GBenign
Select item 707365	NM_000965.5(RARB):c.1316G>C (p.Ser439Thr)	RARB (S327T +5 more)	Single nucleotide variant (missense variant +1 more)	RARB-related disorder +1 more	GBenign
Select item 3051901	NM_000965.5(RARB):c.*4A>G	RARB	Single nucleotide variant (3 prime UTR variant +1 more)	RARB-related disorder	GLikely benign