"Mayo Clinic Laboratories, Mayo Clinic"[submitter] AND "HMOX1"[gene] - ClinVar - NCBI

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Items: 9

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1693775	NM_002133.3(HMOX1):c.-13C>T	HMOX1	Single nucleotide variant (5 prime UTR variant)	not provided	GUncertain significance
Select item 1163763	NM_002133.3(HMOX1):c.-7C>T	HMOX1	Single nucleotide variant (5 prime UTR variant)	not provided	GUncertain significance
Select item 1058925	NM_002133.3(HMOX1):c.131G>A (p.Arg44Gln)	HMOX1 (R44Q)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1427669	NM_002133.3(HMOX1):c.338G>A (p.Arg113His)	HMOX1 (R113H)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2420953	NM_002133.3(HMOX1):c.547C>T (p.Arg183Cys)	HMOX1 (R183C)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1009052	NM_002133.3(HMOX1):c.694C>T (p.Arg232Trp)	HMOX1 (R232W)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1046119	NM_002133.3(HMOX1):c.709C>G (p.Arg237Gly)	HMOX1 (R237G)	Single nucleotide variant (missense variant)	not provided	GConflicting classifications of pathogenicity
Select item 1163764	NM_002133.3(HMOX1):c.715C>T (p.Arg239Trp)	HMOX1 (R239W)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 1441666	NM_002133.3(HMOX1):c.836C>T (p.Ala279Val)	HMOX1 (A279V)	Single nucleotide variant (missense variant)	not provided	GUncertain significance