Related gene-specific medical variations for Gene (Select 253260) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3154234	NM_152756.5(RICTOR):c.4600A>T (p.Ser1534Cys)	OSMR, RICTOR (S1534C +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3025361	NM_152756.5(RICTOR):c.4611G>T (p.Leu1537=)	OSMR, RICTOR	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2512735	NM_152756.5(RICTOR):c.4712C>T (p.Ser1571Leu)	OSMR, RICTOR (S1571L +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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