Related gene-specific medical variations for Gene (Select 441869) - ClinVar

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Items: 29

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3298088	NM_001145210.3(ANKRD65):c.220G>A (p.Gly74Ser)	ANKRD65, ANKRD65-AS1 (G74S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3298066	NM_001145210.3(ANKRD65):c.287G>A (p.Arg96Gln)	ANKRD65, ANKRD65-AS1 (R96Q)	Single nucleotide variant (non-coding transcript variant +2 more)	not specified	GUncertain significance
Select item 3126935	NM_001145210.3(ANKRD65):c.631G>T (p.Ala211Ser)	ANKRD65, ANKRD65-AS1 (A211S)	Single nucleotide variant (non-coding transcript variant +2 more)	not specified	GUncertain significance
Select item 3126934	NM_001145210.3(ANKRD65):c.539C>T (p.Ala180Val)	ANKRD65, ANKRD65-AS1 (A180V)	Single nucleotide variant (non-coding transcript variant +2 more)	not specified	GUncertain significance
Select item 3126933	NM_001145210.3(ANKRD65):c.509C>T (p.Ala170Val)	ANKRD65, ANKRD65-AS1 (A170V)	Single nucleotide variant (non-coding transcript variant +2 more)	not specified	GUncertain significance
Select item 3126932	NM_001145210.3(ANKRD65):c.487C>G (p.Pro163Ala)	ANKRD65, ANKRD65-AS1 (P163A)	Single nucleotide variant (non-coding transcript variant +2 more)	not specified	GUncertain significance
Select item 3126931	NM_001145210.3(ANKRD65):c.440C>A (p.Ala147Asp)	ANKRD65, ANKRD65-AS1 (A147D)	Single nucleotide variant (non-coding transcript variant +2 more)	not specified	GUncertain significance
Select item 2638011	NM_001145210.3(ANKRD65):c.252G>T (p.Arg84=)	ANKRD65, ANKRD65-AS1	Single nucleotide variant (non-coding transcript variant +2 more)	not provided	GLikely benign
Select item 2614959	NM_001145210.3(ANKRD65):c.230C>G (p.Pro77Arg)	ANKRD65, ANKRD65-AS1 (P77R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2553964	NM_001145210.3(ANKRD65):c.502G>A (p.Ala168Thr)	ANKRD65, ANKRD65-AS1 (A168T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2544256	NM_001145210.3(ANKRD65):c.259G>A (p.Ala87Thr)	ANKRD65, ANKRD65-AS1 (A87T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2543706	NM_001145210.3(ANKRD65):c.343G>A (p.Ala115Thr)	ANKRD65, ANKRD65-AS1 (A115T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2493387	NM_001145210.3(ANKRD65):c.314G>A (p.Arg105Gln)	ANKRD65, ANKRD65-AS1 (R105Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2480507	NM_001145210.3(ANKRD65):c.289G>A (p.Gly97Arg)	ANKRD65, ANKRD65-AS1 (G97R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2470092	NM_001145210.3(ANKRD65):c.412G>A (p.Gly138Arg)	ANKRD65, ANKRD65-AS1 (G138R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2468262	NM_001145210.3(ANKRD65):c.224G>C (p.Arg75Pro)	ANKRD65, ANKRD65-AS1 (R75P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2400469	NM_001145210.3(ANKRD65):c.278T>G (p.Leu93Arg)	ANKRD65, ANKRD65-AS1 (L93R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2400468	NM_001145210.3(ANKRD65):c.277C>A (p.Leu93Met)	ANKRD65, ANKRD65-AS1 (L93M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2374922	NM_001145210.3(ANKRD65):c.56G>A (p.Arg19Gln)	ANKRD65, ANKRD65-AS1 (R19Q)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2337935	NM_001145210.3(ANKRD65):c.323G>C (p.Arg108Pro)	ANKRD65, ANKRD65-AS1 (R108P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2336146	NM_001145210.3(ANKRD65):c.106C>T (p.Pro36Ser)	ANKRD65, ANKRD65-AS1 (P36S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2313215	NM_001145210.3(ANKRD65):c.266T>C (p.Leu89Pro)	ANKRD65, ANKRD65-AS1 (L89P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2308857	NM_001145210.3(ANKRD65):c.251G>C (p.Arg84Pro)	ANKRD65, ANKRD65-AS1 (R84P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2289380	NM_001145210.3(ANKRD65):c.251G>A (p.Arg84Gln)	ANKRD65, ANKRD65-AS1 (R84Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2278805	NM_001145210.3(ANKRD65):c.103G>A (p.Gly35Arg)	ANKRD65, ANKRD65-AS1 (G35R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2276768	NM_001145210.3(ANKRD65):c.613G>T (p.Gly205Cys)	ANKRD65, ANKRD65-AS1 (G205C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2257986	NM_001145210.3(ANKRD65):c.210G>C (p.Arg70Ser)	ANKRD65, ANKRD65-AS1 (R70S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2254955	NM_001145210.3(ANKRD65):c.88G>C (p.Gly30Arg)	ANKRD65, ANKRD65-AS1 (G30R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2211294	NM_001145210.3(ANKRD65):c.413G>A (p.Gly138Glu)	ANKRD65, ANKRD65-AS1 (G138E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

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Links from Gene

Items: 29