"Ambry Genetics"[submitter] AND "TBC1D26"[gene] - ClinVar - NCBI

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Items: 15

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2548218	NM_001388465.1(TBC1D26):c.172C>T (p.Pro58Ser)	TBC1D26, TBC1D26-AS1 +1 more (P58S)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2411795	NM_001388465.1(TBC1D26):c.206G>T (p.Arg69Leu)	TBC1D26, TBC1D26-AS1 +1 more (R69L)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2509271	NM_001388465.1(TBC1D26):c.221G>A (p.Arg74His)	TBC1D26, TBC1D26-AS1 +1 more (R74H)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2266997	NM_001388465.1(TBC1D26):c.270C>G (p.Ser90Arg)	TBC1D26, TBC1D26-AS1 +1 more (S90R)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2344278	NM_001388465.1(TBC1D26):c.320G>A (p.Arg107Gln)	TBC1D26, TBC1D26-AS1 +1 more (R107Q)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2520609	NM_001388465.1(TBC1D26):c.326G>A (p.Arg109Gln)	TBC1D26, TBC1D26-AS1 +1 more (R109Q)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GLikely benign
Select item 2461763	NM_001388465.1(TBC1D26):c.346G>C (p.Asp116His)	TBC1D26, TBC1D26-AS1 +1 more (D116H)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3174576	NM_001388465.1(TBC1D26):c.349A>G (p.Ile117Val)	TBC1D26, TBC1D26-AS1 +1 more (I117V)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3174577	NM_001388465.1(TBC1D26):c.440T>C (p.Leu147Pro)	TBC1D26, TBC1D26-AS1 +1 more (L147P)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2568507	NM_001388465.1(TBC1D26):c.470T>G (p.Met157Arg)	TBC1D26, TBC1D26-AS1 +1 more (M157R)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3174578	NM_001388465.1(TBC1D26):c.518T>A (p.Ile173Asn)	TBC1D26, TBC1D26-AS1 +1 more (I173N)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3174579	NM_001388465.1(TBC1D26):c.527C>A (p.Ala176Asp)	TBC1D26, TBC1D26-AS1 +1 more (A176D)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2303464	NM_001388465.1(TBC1D26):c.581C>T (p.Thr194Ile)	TBC1D26, TBC1D26-AS1 +1 more (T194I)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2614742	NM_001388465.1(TBC1D26):c.584C>T (p.Ala195Val)	TBC1D26, TBC1D26-AS1 +1 more (A195V)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2352130	NM_001388465.1(TBC1D26):c.675C>T (p.Leu225=)	TBC1D26, TBC1D26-AS1 +1 more (S232L)	Single nucleotide variant (non-coding transcript variant +2 more)	not specified	GLikely benign