"Ambry Genetics"[submitter] AND "NDUFB9"[gene] - ClinVar - NCBI

Warning: The NCBI web site requires JavaScript to function. more...

Search results

Items: 11

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1928975	NM_005005.3(NDUFB9):c.11T>G (p.Leu4Trp)	NDUFB9 (L4W)	Single nucleotide variant (5 prime UTR variant +1 more)	not provided +1 more	GUncertain significance
Select item 2306459	NM_005005.3(NDUFB9):c.65G>A (p.Arg22Gln)	NDUFB9 (R22Q)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2552188	NM_005005.3(NDUFB9):c.79C>G (p.Leu27Val)	NDUFB9 (L27V)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3188007	NM_005005.3(NDUFB9):c.103G>C (p.Asp35His)	NDUFB9 (D35H)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 1525100	NM_005005.3(NDUFB9):c.171G>A (p.Met57Ile)	NDUFB9 (M1I +3 more)	Single nucleotide variant (missense variant +1 more)	not specified +1 more	GUncertain significance
Select item 3188017	NM_005005.3(NDUFB9):c.186G>C (p.Gln62His)	NDUFB9 (Q62H +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3299063	NM_005005.3(NDUFB9):c.221G>A (p.Arg74His)	NDUFB9 (R63H +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1960418	NM_005005.3(NDUFB9):c.256C>T (p.Pro86Ser)	NDUFB9 (P86S +3 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2167590	NM_005005.3(NDUFB9):c.307T>G (p.Cys103Gly)	NDUFB9 (C92G +3 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2520878	NM_005005.3(NDUFB9):c.373T>G (p.Trp125Gly)	NDUFB9 (W114G +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1049847	NM_005005.3(NDUFB9):c.536T>C (p.Met179Thr)	NDUFB9 (M123T +3 more)	Single nucleotide variant (missense variant)	not specified +1 more	GConflicting classifications of pathogenicity