Related gene-specific medical variations for Gene (Select 387990) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3328015	NM_207377.3(TOMM20L):c.88A>G (p.Asn30Asp)	LOC130055732, TOMM20L (N30D)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3181128	NM_207377.3(TOMM20L):c.66C>G (p.Phe22Leu)	LOC130055732, TOMM20L (F22L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3177564	NM_012460.4(TIMM9):c.200T>G (p.Phe67Cys)	TIMM9, TOMM20L (F67C)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2605073	NM_207377.3(TOMM20L):c.451C>A (p.Pro151Thr)	TIMM9, TOMM20L (P151T)	Single nucleotide variant (3 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 2367584	NM_207377.3(TOMM20L):c.104G>A (p.Gly35Glu)	LOC130055732, TOMM20L (G35E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2279652	NM_207377.3(TOMM20L):c.25C>G (p.Arg9Gly)	LOC130055732, TOMM20L (R9G)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2262989	NM_207377.3(TOMM20L):c.100C>G (p.Arg34Gly)	LOC130055732, TOMM20L (R34G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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