Related gene-specific medical variations for Gene (Select 55269) - ClinVar - NCBI

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Items: 4

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3295690	NM_017520.4(MPHOSPH8):c.2573A>G (p.Gln858Arg)	MPHOSPH8, PSPC1 (Q858R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3202054	NM_017520.4(MPHOSPH8):c.2476T>C (p.Ser826Pro)	MPHOSPH8, PSPC1 (S826P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2488527	NM_017520.4(MPHOSPH8):c.2497C>G (p.Pro833Ala)	MPHOSPH8, PSPC1 (P833A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2318892	NM_017520.4(MPHOSPH8):c.2489T>C (p.Val830Ala)	MPHOSPH8, PSPC1 (V830A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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