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

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Items: 12

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3300133	NM_021077.4(NMB):c.*84C>G	NMB (P149A)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3200773	NM_021077.4(NMB):c.*37A>T	NMB (D133V)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2316041	NM_021077.4(NMB):c.314C>G (p.Pro105Arg)	NMB (P105R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3200772	NM_021077.4(NMB):c.230T>C (p.Leu77Pro)	NMB (L77P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3200771	NM_021077.4(NMB):c.203C>T (p.Pro68Leu)	NMB (P68L)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2301557	NM_021077.4(NMB):c.200C>T (p.Ser67Phe)	NMB (S67F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2596463	NM_021077.4(NMB):c.187C>G (p.Pro63Ala)	NMB (P63A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2523869	NM_021077.4(NMB):c.158G>T (p.Gly53Val)	NMB (G53V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2598025	NM_021077.4(NMB):c.132C>G (p.His44Gln)	NMB (H44Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3200774	NM_021077.4(NMB):c.61G>C (p.Ala21Pro)	NMB (A21P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3300134	NM_021077.4(NMB):c.52G>A (p.Ala18Thr)	NMB (A18T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2521837	NM_021077.4(NMB):c.7C>T (p.Arg3Trp)	NMB (R3W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance