Related gene-specific medical variations for Gene (Select 115209) - ClinVar - NCBI

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Items: 11

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2638845	NM_145243.5(OMA1):c.1349A>T (p.Asp450Val)	DAB1, OMA1 (D450V)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign
Select item 1287065	NM_145243.5(OMA1):c.632T>G (p.Phe211Cys)	DAB1, OMA1 (F211C)	Single nucleotide variant (missense variant +1 more)	not provided	GBenign
Select item 785790	NM_145243.5(OMA1):c.924C>T (p.Phe308=)	DAB1, OMA1	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 780242	NM_145243.5(OMA1):c.201C>A (p.Asn67Lys)	DAB1, OMA1 (N67K)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 780241	NM_145243.5(OMA1):c.595T>C (p.Leu199=)	DAB1, OMA1	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 780003	NM_145243.5(OMA1):c.1366-9T>G	DAB1, OMA1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 773636	NM_145243.5(OMA1):c.880A>G (p.Ile294Val)	DAB1, OMA1 (I294V)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 767673	NM_145243.5(OMA1):c.205C>T (p.His69Tyr)	DAB1, OMA1 (H69Y)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 729080	NM_145243.5(OMA1):c.755T>C (p.Met252Thr)	DAB1, OMA1 (M252T)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 722109	NM_145243.5(OMA1):c.1565C>T (p.Thr522Met)	DAB1, OMA1 (T522M)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 713749	NM_145243.5(OMA1):c.1093G>T (p.Asp365Tyr)	DAB1, OMA1 (D365Y)	Single nucleotide variant (missense variant)	not provided	GLikely benign