ANKRD65[gene] and "single gene"[properties] - ClinVar

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Items: 28

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3126929	NM_001145210.3(ANKRD65):c.1187A>T (p.Glu396Val)	ANKRD65 (E396V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2373561	NM_001145210.3(ANKRD65):c.1160G>T (p.Gly387Val)	ANKRD65 (G387V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2349709	NM_001145210.3(ANKRD65):c.1160G>C (p.Gly387Ala)	ANKRD65 (G387A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3126928	NM_001145210.3(ANKRD65):c.1159G>T (p.Gly387Trp)	ANKRD65 (G387W)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2481928	NM_001145210.3(ANKRD65):c.1147C>T (p.Pro383Ser)	ANKRD65 (P383S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2638008	NM_001145210.3(ANKRD65):c.1142C>T (p.Ala381Val)	ANKRD65 (A381V)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign
Select item 2377909	NM_001145210.3(ANKRD65):c.1091G>A (p.Arg364Gln)	ANKRD65 (R364Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2209875	NM_001145210.3(ANKRD65):c.1070G>A (p.Arg357Gln)	ANKRD65 (R357Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3298058	NM_001145210.3(ANKRD65):c.1069C>G (p.Arg357Gly)	ANKRD65 (R357G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2614958	NM_001145210.3(ANKRD65):c.1036G>T (p.Gly346Trp)	ANKRD65 (G346W +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2638009	NM_001145210.3(ANKRD65):c.963G>C (p.Leu321=)	ANKRD65 (C141S)	Single nucleotide variant (synonymous variant +2 more)	not provided	GLikely benign
Select item 2524814	NM_001145210.3(ANKRD65):c.955G>A (p.Gly319Ser)	ANKRD65 (G319S)	Single nucleotide variant (missense variant +2 more)	not specified	GLikely benign
Select item 2209697	NM_001145210.3(ANKRD65):c.932G>A (p.Arg311Gln)	ANKRD65 (G131R +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3298098	NM_001145210.3(ANKRD65):c.931C>T (p.Arg311Trp)	ANKRD65 (R311W)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2526305	NM_001145210.3(ANKRD65):c.893G>A (p.Arg298Gln)	ANKRD65 (G118R +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 3126938	NM_001145210.3(ANKRD65):c.880G>A (p.Glu294Lys)	ANKRD65 (E294K)	Single nucleotide variant (missense variant +2 more)	not specified	GLikely benign
Select item 3298105	NM_001145210.3(ANKRD65):c.863T>C (p.Leu288Pro)	ANKRD65 (L288P +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2514931	NM_001145210.3(ANKRD65):c.832G>A (p.Ala278Thr)	ANKRD65 (A278T)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2520861	NM_001145210.3(ANKRD65):c.815C>A (p.Ala272Glu)	ANKRD65 (A272E +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2515587	NM_001145210.3(ANKRD65):c.788G>A (p.Gly263Asp)	ANKRD65 (A83T +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2485522	NM_001145210.3(ANKRD65):c.775G>A (p.Gly259Arg)	ANKRD65 (G259R)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2638010	NM_001145210.3(ANKRD65):c.729G>A (p.Ala243=)	ANKRD65	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 3126936	NM_001145210.3(ANKRD65):c.718C>A (p.Leu240Met)	ANKRD65 (L240M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2473491	NM_001145210.3(ANKRD65):c.677G>C (p.Gly226Ala)	ANKRD65 (G226A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2473490	NM_001145210.3(ANKRD65):c.676G>C (p.Gly226Arg)	ANKRD65 (G226R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2476165	NM_001145210.3(ANKRD65):c.673C>A (p.Arg225Ser)	ANKRD65 (R225S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3298049	NM_001145210.3(ANKRD65):c.659G>A (p.Arg220His)	ANKRD65 (R220H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3298077	NM_001145210.3(ANKRD65):c.652G>A (p.Ala218Thr)	ANKRD65 (A218T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

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Items: 28