Related gene-specific medical variations for Gene (Select 6189) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3315299	NM_001006.5(RPS3A):c.104C>T (p.Ala35Val)	LOC126807190, RPS3A (A35V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3156190	NM_001006.5(RPS3A):c.29C>G (p.Thr10Arg)	RPS3A, LOC126807190 (T10R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 778160	NM_001006.5(RPS3A):c.63-6A>T	LOC126807190, RPS3A	Single nucleotide variant (intron variant)	not provided	GBenign

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