Related gene-specific medical variations for Gene (Select 101926934) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3163664	NM_004277.5(SLC25A27):c.936A>C (p.Glu312Asp)	SLC25A27, TDRD6-AS1 (E312D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3163663	NM_004277.5(SLC25A27):c.861G>T (p.Met287Ile)	SLC25A27, TDRD6-AS1 (M287I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2624145	NM_004277.5(SLC25A27):c.913A>G (p.Met305Val)	SLC25A27, TDRD6-AS1 (M305V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2604372	NM_001010870.3(TDRD6):c.8C>T (p.Ser3Leu)	TDRD6, TDRD6-AS1 (S3L)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2493511	NM_004277.5(SLC25A27):c.832A>G (p.Ile278Val)	SLC25A27, TDRD6-AS1 (I278V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2336505	NM_004277.5(SLC25A27):c.830T>C (p.Leu277Ser)	SLC25A27, TDRD6-AS1 (L277S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2281249	NM_004277.5(SLC25A27):c.800G>A (p.Gly267Glu)	SLC25A27, TDRD6-AS1 (G267E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

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