Related gene-specific medical variations for Gene (Select 10966) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2297030	NM_006822.3(RAB40B):c.115G>A (p.Ala39Thr)	LOC130062056, RAB40B (A39T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2286761	NM_006822.3(RAB40B):c.109G>A (p.Gly37Ser)	LOC130062056, RAB40B (G37S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2231504	NM_006822.3(RAB40B):c.137C>T (p.Pro46Leu)	LOC130062056, RAB40B (P46L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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