BAIAP2[gene] and "single gene"[properties] - ClinVar

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Items: 46

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2557754	NM_001144888.2(BAIAP2):c.47T>A (p.Val16Asp)	BAIAP2 (V16D)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2507410	NM_001144888.2(BAIAP2):c.54+45T>C	BAIAP2	Single nucleotide variant (intron variant)	Attention deficit hyperactivity disorder	GUncertain significance
Select item 3132859	NM_001144888.2(BAIAP2):c.260A>G (p.Gln87Arg)	BAIAP2 (Q112R +4 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2461800	NM_001144888.2(BAIAP2):c.330G>T (p.Glu110Asp)	BAIAP2 (E52D +5 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3132860	NM_001144888.2(BAIAP2):c.389A>G (p.Lys130Arg)	BAIAP2 (K128R +5 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 735383	NM_001144888.2(BAIAP2):c.462T>A (p.Pro154=)	BAIAP2	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 2507408	NM_001144888.2(BAIAP2):c.490-1717A>G	BAIAP2	Single nucleotide variant (intron variant)	Attention deficit hyperactivity disorder	GUncertain significance
Select item 735929	NM_001144888.2(BAIAP2):c.519C>T (p.Gly173=)	BAIAP2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 778754	NM_001144888.2(BAIAP2):c.555C>T (p.Thr185=)	BAIAP2	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 711694	NM_001144888.2(BAIAP2):c.612G>A (p.Val204=)	BAIAP2	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 736258	NM_001144888.2(BAIAP2):c.624C>T (p.Ser208=)	BAIAP2	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 720773	NM_001144888.2(BAIAP2):c.643-9C>T	BAIAP2	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 2352170	NM_001144888.2(BAIAP2):c.671C>T (p.Pro224Leu)	BAIAP2 (P166L +5 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3132861	NM_001144888.2(BAIAP2):c.719C>T (p.Ala240Val)	BAIAP2 (A182V +5 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3132862	NM_001144888.2(BAIAP2):c.751G>A (p.Gly251Ser)	BAIAP2 (G173S +6 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2355154	NM_001144888.2(BAIAP2):c.754G>A (p.Ala252Thr)	BAIAP2 (A250T +6 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2386124	NM_001144888.2(BAIAP2):c.889C>A (p.Pro297Thr)	BAIAP2 (P239T +6 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 734861	NM_001144888.2(BAIAP2):c.900C>T (p.Asn300=)	BAIAP2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2206750	NM_001144888.2(BAIAP2):c.904G>A (p.Val302Ile)	BAIAP2 (V244I +6 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2489188	NM_001144888.2(BAIAP2):c.929A>G (p.Tyr310Cys)	BAIAP2 (Y343C +6 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3132863	NM_001144888.2(BAIAP2):c.934C>T (p.Pro312Ser)	BAIAP2 (P312S +6 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3132864	NM_001144888.2(BAIAP2):c.974C>G (p.Ser325Cys)	BAIAP2 (S267C +6 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3132865	NM_001144888.2(BAIAP2):c.986C>T (p.Ser329Phe)	BAIAP2 (S271F +6 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3132866	NM_001144888.2(BAIAP2):c.997C>T (p.Leu333Phe)	BAIAP2 (L358F +6 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3132856	NM_001144888.2(BAIAP2):c.1039G>A (p.Val347Met)	BAIAP2 (V289M +6 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2334201	NM_001144888.2(BAIAP2):c.1058A>G (p.Tyr353Cys)	BAIAP2 (Y275C +6 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2389733	NM_001144888.2(BAIAP2):c.1076A>G (p.Lys359Arg)	BAIAP2 (K359R +9 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 730621	NM_001144888.2(BAIAP2):c.1176C>T (p.Thr392=)	BAIAP2	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 742546	NM_001144888.2(BAIAP2):c.1203C>G (p.Leu401=)	BAIAP2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 738783	NM_001144888.2(BAIAP2):c.1269-7C>T	BAIAP2	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2530727	NM_001144888.2(BAIAP2):c.1333A>G (p.Met445Val)	BAIAP2 (M443V +9 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 757588	NM_001144888.2(BAIAP2):c.1337+10G>A	BAIAP2	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2493806	NM_001144888.2(BAIAP2):c.1343A>G (p.Gln448Arg)	BAIAP2 (Q205R +9 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 717517	NM_001144888.2(BAIAP2):c.1347A>G (p.Gln449=)	BAIAP2	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 2510934	NM_001144888.2(BAIAP2):c.1390C>A (p.Leu464Met)	BAIAP2 (L387M +9 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2547828	NM_001144888.2(BAIAP2):c.1412A>G (p.Tyr471Cys)	BAIAP2 (Y504C +10 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2291983	NM_001144888.2(BAIAP2):c.1427G>A (p.Arg476Gln)	BAIAP2 (R476Q +10 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2222982	NM_001144888.2(BAIAP2):c.1438G>A (p.Ala480Thr)	BAIAP2 (A422T +9 more)	Single nucleotide variant (missense variant +2 more)	not specified	GLikely benign
Select item 2507411	NM_001144888.2(BAIAP2):c.1535+553G>A	BAIAP2	Single nucleotide variant (intron variant +2 more)	Attention deficit hyperactivity disorder	GUncertain significance
Select item 2507409	NM_001144888.2(BAIAP2):c.1535+1763T>G	BAIAP2	Single nucleotide variant (3 prime UTR variant +2 more)	Attention deficit hyperactivity disorder	GUncertain significance
Select item 2470969	NM_001144888.2(BAIAP2):c.1552G>A (p.Val518Ile)	BAIAP2 (V460I +5 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 781873	NM_001144888.2(BAIAP2):c.1566G>A (p.Pro522=)	BAIAP2	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 3132858	NM_001144888.2(BAIAP2):c.*432G>A	BAIAP2 (G542E +1 more)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2325537	NM_001144888.2(BAIAP2):c.*434G>C	BAIAP2 (D543H +1 more)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2397626	NM_001144888.2(BAIAP2):c.*446C>T	BAIAP2 (R547C +1 more)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GLikely benign
Select item 2370249	NM_001144888.2(BAIAP2):c.*458G>A	BAIAP2 (G584R +1 more)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance

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Items: 46