TMEM9B[gene] and "single gene"[properties] - ClinVar - NCBI

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Items: 5

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3179772	NM_020644.3(TMEM9B):c.502G>A (p.Val168Met)	TMEM9B (V168M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3179771	NM_020644.3(TMEM9B):c.469G>A (p.Asp157Asn)	TMEM9B (D83N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3179770	NM_020644.3(TMEM9B):c.418A>C (p.Ile140Leu)	TMEM9B (I66L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2307261	NM_020644.3(TMEM9B):c.283G>C (p.Glu95Gln)	TMEM9B (E95Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3179769	NM_020644.3(TMEM9B):c.262C>T (p.Arg88Cys)	TMEM9B (R14C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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