Related gene-specific medical variations for Gene (Select 728591) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3264057	NM_001144981.3(CCDC169):c.61T>G (p.Leu21Val)	CCDC169, CCDC169-SOHLH2 (L21V)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3264056	NM_001144981.3(CCDC169):c.113T>C (p.Leu38Pro)	CCDC169, CCDC169-SOHLH2 (L38P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3138770	NM_001144981.3(CCDC169):c.145C>T (p.Leu49Phe)	CCDC169, CCDC169-SOHLH2 (L49F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2494924	NM_001198908.2(CCDC169):c.721A>G (p.Ser241Gly)	CCDC169, CCDC169-SOHLH2 (S139G +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2470484	NM_001144981.3(CCDC169):c.181C>T (p.Arg61Cys)	CCDC169, CCDC169-SOHLH2 (R61C)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2343749	NM_001144981.3(CCDC169):c.23A>G (p.Asn8Ser)	CCDC169, CCDC169-SOHLH2 (N8S)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2335637	NM_001144981.3(CCDC169):c.20A>G (p.Tyr7Cys)	CCDC169, CCDC169-SOHLH2 (Y7C)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance

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