MZT2B[gene] and "single gene"[properties] - ClinVar - NCBI

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Items: 14

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3170427	NM_025029.5(MZT2B):c.199G>A (p.Val67Met)	MZT2B (V67M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2305269	NM_025029.5(MZT2B):c.219C>G (p.Phe73Leu)	MZT2B (F73L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3298212	NM_025029.5(MZT2B):c.241G>A (p.Ala81Thr)	MZT2B (A81T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2525824	NM_025029.5(MZT2B):c.278C>T (p.Ala93Val)	MZT2B (A93V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3298214	NM_025029.5(MZT2B):c.292C>T (p.Pro98Ser)	MZT2B (P98S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2253722	NM_025029.5(MZT2B):c.308C>T (p.Pro103Leu)	MZT2B (P103L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2651363	NM_025029.5(MZT2B):c.319+1061C>G	MZT2B	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2651364	NM_025029.5(MZT2B):c.319+1145C>G	MZT2B	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 3298210	NM_025029.5(MZT2B):c.325A>G (p.Asn109Asp)	MZT2B (K59R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3298215	NM_025029.5(MZT2B):c.337G>A (p.Ala113Thr)	MZT2B (A113T +2 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3170436	NM_025029.5(MZT2B):c.355T>A (p.Leu119Met)	MZT2B (L119M +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3170440	NM_025029.5(MZT2B):c.382G>A (p.Glu128Lys)	MZT2B (R78Q +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3298211	NM_025029.5(MZT2B):c.406C>T (p.Arg136Cys)	MZT2B (R196C +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3170447	NM_025029.5(MZT2B):c.460A>G (p.Thr154Ala)	MZT2B (Y104C +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance