"Ambry Genetics"[submitter] AND "SLC25A31"[gene] - ClinVar - NCBI

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Items: 17

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3163684	NM_031291.4(SLC25A31):c.14C>T (p.Pro5Leu)	SLC25A31 (P5L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3163683	NM_031291.4(SLC25A31):c.104A>G (p.Lys35Arg)	SLC25A31 (K35R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2546842	NM_031291.4(SLC25A31):c.127C>T (p.Arg43Trp)	SLC25A31 (R43W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2315792	NM_031291.4(SLC25A31):c.206G>A (p.Cys69Tyr)	SLC25A31 (C69Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2345534	NM_031291.4(SLC25A31):c.208C>G (p.Leu70Val)	SLC25A31 (L70V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2357249	NM_031291.4(SLC25A31):c.278A>G (p.Tyr93Cys)	SLC25A31 (Y93C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2304125	NM_031291.4(SLC25A31):c.363C>G (p.Phe121Leu)	SLC25A31 (F121L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2375964	NM_031291.4(SLC25A31):c.366G>T (p.Trp122Cys)	SLC25A31 (W122C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2557738	NM_031291.4(SLC25A31):c.403G>T (p.Ala135Ser)	SLC25A31 (A135S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3163685	NM_031291.4(SLC25A31):c.466G>A (p.Asp156Asn)	SLC25A31 (D156N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2328540	NM_031291.4(SLC25A31):c.523A>C (p.Lys175Gln)	SLC25A31 (K175Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2366131	NM_031291.4(SLC25A31):c.662C>T (p.Pro221Leu)	SLC25A31 (P221L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3163686	NM_031291.4(SLC25A31):c.715C>T (p.Leu239Phe)	SLC25A31 (L239F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2371966	NM_031291.4(SLC25A31):c.734C>T (p.Thr245Ile)	SLC25A31 (T245I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2349605	NM_031291.4(SLC25A31):c.775C>T (p.Arg259Trp)	SLC25A31 (R259W)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3319224	NM_031291.4(SLC25A31):c.859A>G (p.Asn287Asp)	SLC25A31 (N287D)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2204130	NM_031291.4(SLC25A31):c.926A>G (p.His309Arg)	SLC25A31 (H309R)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance