"BRD2-related condition"[Disease/phenotype] AND "PreventionGenetics, p - ClinVar - NCBI

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Items: 18

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 726131	NM_005104.4(BRD2):c.55T>C (p.Leu19=)	BRD2	Single nucleotide variant (synonymous variant +1 more)	BRD2-related condition +1 more	GBenign
Select item 3058972	NM_005104.4(BRD2):c.93G>A (p.Lys31=)	BRD2	Single nucleotide variant (synonymous variant +1 more)	BRD2-related condition	GBenign
Select item 772878	NM_005104.4(BRD2):c.201C>T (p.Ser67=)	BRD2	Single nucleotide variant (synonymous variant +1 more)	BRD2-related condition +1 more	GBenign
Select item 722120	NM_005104.4(BRD2):c.285C>T (p.Phe95=)	BRD2	Single nucleotide variant (synonymous variant +1 more)	BRD2-related condition +1 more	GLikely benign
Select item 3060819	NM_005104.4(BRD2):c.334-10T>C	BRD2	Single nucleotide variant (intron variant)	BRD2-related condition	GBenign
Select item 3044768	NM_005104.4(BRD2):c.459C>T (p.Tyr153=)	BRD2	Single nucleotide variant (synonymous variant)	BRD2-related condition	GLikely benign
Select item 3049144	NM_005104.4(BRD2):c.472-5C>T	BRD2	Single nucleotide variant (intron variant)	BRD2-related condition	GLikely benign
Select item 770728	NM_005104.4(BRD2):c.611-4C>G	BRD2	Single nucleotide variant (intron variant)	not provided +1 more	GBenign/Likely benign
Select item 786735	NM_005104.4(BRD2):c.621C>T (p.Gly207=)	BRD2	Single nucleotide variant (synonymous variant)	BRD2-related condition +1 more	GBenign
Select item 785805	NM_005104.4(BRD2):c.712C>T (p.Leu238Phe)	BRD2 (L118F +2 more)	Single nucleotide variant (missense variant)	BRD2-related condition +1 more	GBenign
Select item 95242	NM_005104.4(BRD2):c.1330-4G>C	BRD2	Single nucleotide variant (intron variant)	BRD2-related condition +1 more	GBenign
Select item 3055955	NM_005104.4(BRD2):c.1421C>T (p.Ala474Val)	BRD2 (A354V +2 more)	Single nucleotide variant (missense variant +1 more)	BRD2-related condition	GBenign
Select item 95243	NM_005104.4(BRD2):c.1497GGA[1] (p.Glu500del)	BRD2 (E500del +2 more)	Microsatellite (inframe_deletion)	BRD2-related condition +1 more	GConflicting classifications of pathogenicity
Select item 752758	NM_005104.4(BRD2):c.1515A>G (p.Glu505=)	BRD2	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign
Select item 715423	NM_005104.4(BRD2):c.1705G>A (p.Ala569Thr)	BRD2 (A522T +2 more)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign
Select item 3060697	NM_005104.4(BRD2):c.1710T>C (p.Asp570=)	BRD2	Single nucleotide variant (synonymous variant)	BRD2-related condition	GBenign
Select item 3059565	NM_005104.4(BRD2):c.1809T>C (p.Ser603=)	BRD2	Single nucleotide variant (synonymous variant)	BRD2-related condition	GBenign
Select item 778338	NM_005104.4(BRD2):c.2296G>A (p.Ala766Thr)	BRD2 (A766T +3 more)	Single nucleotide variant (missense variant)	BRD2-related condition +1 more	GBenign/Likely benign