ANKRD2[gene] and "single gene"[properties] - ClinVar

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Items: 27

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 768382	NM_001291218.2(ANKRD2):c.17C>G (p.Pro6Arg)	ANKRD2 (P6R)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 776534	NM_001291218.2(ANKRD2):c.173_175del (p.Trp58_Pro59delinsSer)	ANKRD2	Deletion (5 prime UTR variant +1 more)	not provided	GBenign
Select item 3123934	NM_020349.4(ANKRD2):c.34G>A (p.Ala12Thr)	ANKRD2 (A98T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2301761	NM_020349.4(ANKRD2):c.67C>T (p.Pro23Ser)	ANKRD2 (P109S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2265751	NM_001346793.2(ANKRD2):c.25G>A (p.Glu9Lys)	ANKRD2 (E9K +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3123897	NM_001346793.2(ANKRD2):c.29C>T (p.Ala10Val)	ANKRD2 (A10V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3123903	NM_001346793.2(ANKRD2):c.34C>A (p.Gln12Lys)	ANKRD2 (Q12K +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3296660	NM_001346793.2(ANKRD2):c.54C>G (p.Ile18Met)	ANKRD2 (I18M +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2211870	NM_001346793.2(ANKRD2):c.100G>A (p.Asp34Asn)	ANKRD2 (D34N +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3123918	NM_001346793.2(ANKRD2):c.125A>T (p.Asp42Val)	ANKRD2 (D155V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3123928	NM_001346793.2(ANKRD2):c.223C>G (p.Leu75Val)	ANKRD2 (L102V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2640739	NM_001346793.2(ANKRD2):c.315C>G (p.Ala105=)	ANKRD2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 774685	NM_001346793.2(ANKRD2):c.356C>T (p.Pro119Leu)	ANKRD2 (P119L +2 more)	Single nucleotide variant (missense variant)	not provided	GBenign/Likely benign
Select item 2478666	NM_001346793.2(ANKRD2):c.392A>T (p.Glu131Val)	ANKRD2 (E131V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3123942	NM_001346793.2(ANKRD2):c.395G>A (p.Gly132Glu)	ANKRD2 (G132E +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3123948	NM_001346793.2(ANKRD2):c.430G>T (p.Gly144Trp)	ANKRD2 (G171W +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2369852	NM_001346793.2(ANKRD2):c.464G>A (p.Arg155Gln)	ANKRD2 (R155Q +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2243536	NM_001346793.2(ANKRD2):c.604G>T (p.Val202Leu)	ANKRD2 (V202L +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2513416	NM_001346793.2(ANKRD2):c.697G>A (p.Val233Met)	ANKRD2 (V346M +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3296642	NM_001346793.2(ANKRD2):c.741T>A (p.Asn247Lys)	ANKRD2 (N247K +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 773005	NM_001346793.2(ANKRD2):c.855A>G (p.Ala285=)	ANKRD2	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 3123964	NM_001346793.2(ANKRD2):c.866C>T (p.Pro289Leu)	ANKRD2 (P256L +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3296650	NM_001346793.2(ANKRD2):c.882G>C (p.Gln294His)	ANKRD2 (Q288H +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2295879	NM_001346793.2(ANKRD2):c.888G>C (p.Trp296Cys)	ANKRD2 (W290C +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2561447	NM_001346793.2(ANKRD2):c.890A>T (p.Gln297Leu)	ANKRD2 (Q291L +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2536723	NM_001346793.2(ANKRD2):c.932C>T (p.Ala311Val)	ANKRD2 (A305V +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3123894	NM_001346793.2(ANKRD2):c.935A>G (p.Glu312Gly)	ANKRD2 (E425G +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 27