HHLA2[gene] and "single gene"[properties] - ClinVar

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Items: 29

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2300733	NM_001282556.2(HHLA2):c.31C>G (p.Leu11Val)	HHLA2 (L11V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3105761	NM_001282556.2(HHLA2):c.78G>T (p.Leu26Phe)	HHLA2 (L26F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2344527	NM_001282556.2(HHLA2):c.115G>A (p.Val39Ile)	HHLA2 (V39I)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2550168	NM_001282556.2(HHLA2):c.272G>T (p.Arg91Met)	HHLA2 (R91M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2400619	NM_001282556.2(HHLA2):c.482T>C (p.Val161Ala)	HHLA2 (V161A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2374417	NM_001282556.2(HHLA2):c.487A>G (p.Ser163Gly)	HHLA2 (S163G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2354000	NM_001282556.2(HHLA2):c.497C>T (p.Pro166Leu)	HHLA2 (P102L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2208893	NM_001282556.2(HHLA2):c.552G>A (p.Met184Ile)	HHLA2 (M184I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2358213	NM_001282556.2(HHLA2):c.562G>C (p.Gly188Arg)	HHLA2 (G124R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3105757	NM_001282556.2(HHLA2):c.586A>G (p.Asn196Asp)	HHLA2 (N196D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3105758	NM_001282556.2(HHLA2):c.608G>A (p.Gly203Glu)	HHLA2 (G139E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2623314	NM_001282556.2(HHLA2):c.635T>C (p.Ile212Thr)	HHLA2 (I212T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3105759	NM_001282556.2(HHLA2):c.641A>T (p.Asn214Ile)	HHLA2 (N214I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2316080	NM_001282556.2(HHLA2):c.670C>T (p.Arg224Cys)	HHLA2 (R224C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2371845	NM_001282556.2(HHLA2):c.677C>T (p.Thr226Met)	HHLA2 (T162M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2561844	NM_001282556.2(HHLA2):c.697A>G (p.Lys233Glu)	HHLA2 (K233E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3284250	NM_001282556.2(HHLA2):c.702G>T (p.Met234Ile)	HHLA2 (M170I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2622644	NM_001282556.2(HHLA2):c.715G>A (p.Val239Ile)	HHLA2 (V175I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3284251	NM_001282556.2(HHLA2):c.793A>T (p.Ser265Cys)	HHLA2 (S265C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2455811	NM_001282556.2(HHLA2):c.817T>A (p.Tyr273Asn)	HHLA2 (Y273N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3105762	NM_001282556.2(HHLA2):c.854A>G (p.Glu285Gly)	HHLA2 (E285G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3105763	NM_001282556.2(HHLA2):c.860G>A (p.Arg287Gln)	HHLA2 (R287Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2281036	NM_001282556.2(HHLA2):c.890A>G (p.Gln297Arg)	HHLA2 (Q297R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2246983	NM_001282556.2(HHLA2):c.917A>G (p.Asp306Gly)	HHLA2 (D242G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3284252	NM_001282556.2(HHLA2):c.1081C>A (p.Leu361Met)	HHLA2 (L297M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3105756	NM_001282556.2(HHLA2):c.1093G>A (p.Val365Ile)	HHLA2 (V365I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2265297	NM_001282556.2(HHLA2):c.1181G>T (p.Gly394Val)	HHLA2 (G330V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2207807	NM_001282556.2(HHLA2):c.1186C>T (p.Arg396Cys)	HHLA2 (R332C +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2395578	NM_001282556.2(HHLA2):c.1211G>A (p.Gly404Asp)	HHLA2 (G404D +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 29