Related gene-specific medical variations for Gene (Select 26521) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3177563	NM_012459.4(TIMM8B):c.31G>A (p.Glu11Lys)	LOC126861339, TIMM8B (E11K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3177562	NM_012459.4(TIMM8B):c.2T>C (p.Met1Thr)	LOC126861339, TIMM8B (M1T)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3177561	NM_012459.4(TIMM8B):c.-8G>C	LOC126861339, TIMM8B	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GLikely benign
Select item 3177560	NM_012459.4(TIMM8B):c.-15A>G	LOC126861339, TIMM8B	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3177556	NM_012459.4(TIMM8B):c.56A>T (p.Glu19Val)	LOC126861339, TIMM8B (E19V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2397089	NM_012459.4(TIMM8B):c.65A>G (p.Lys22Arg)	LOC126861339, TIMM8B (K22R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2295604	NM_012459.4(TIMM8B):c.-32G>A	LOC126861339, TIMM8B	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance

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