Related gene-specific medical variations for Gene (Select 83937) - ClinVar - NCBI

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Items: 5

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3081760	NM_007021.4(DEPP1):c.548C>T (p.Ser183Phe)	DEPP1, RASSF4 (S183F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3081759	NM_007021.4(DEPP1):c.262C>T (p.Arg88Cys)	DEPP1, RASSF4 (R88C)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 3081758	NM_007021.4(DEPP1):c.25G>A (p.Val9Met)	DEPP1, RASSF4 (V9M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3081757	NM_007021.4(DEPP1):c.248G>A (p.Arg83Gln)	DEPP1, RASSF4 (R83Q)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 786154	NM_007021.4(DEPP1):c.301A>G (p.Thr101Ala)	DEPP1, RASSF4 (T101A)	Single nucleotide variant (missense variant +1 more)	not provided	GBenign

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