Related gene-specific medical variations for Gene (Select 221301) - ClinVar - NCBI

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Items: 4

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3328533	NM_001139444.3(TRAPPC3L):c.35A>G (p.His12Arg)	CALHM4, TRAPPC3L (H12R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3181997	NM_001139444.3(TRAPPC3L):c.52C>T (p.Leu18Phe)	CALHM4, TRAPPC3L (L18F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3181995	NM_001139444.3(TRAPPC3L):c.224T>C (p.Ile75Thr)	CALHM4, TRAPPC3L (I75T)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2327156	NM_001139444.3(TRAPPC3L):c.62T>C (p.Leu21Pro)	CALHM4, TRAPPC3L (L21P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

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