Related gene-specific medical variations for Gene (Select 25950) - ClinVar - NCBI

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Items: 11

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3157263	NM_015485.5(RWDD3):c.92A>G (p.Asp31Gly)	RWDD3, TLCD4-RWDD3 (D16G +1 more)	Single nucleotide variant (synonymous variant +2 more)	not specified	GUncertain significance
Select item 3157262	NM_015485.5(RWDD3):c.182A>G (p.Tyr61Cys)	RWDD3, TLCD4-RWDD3 (Y46C +1 more)	Single nucleotide variant (3 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 3157261	NM_015485.5(RWDD3):c.138T>G (p.Asp46Glu)	RWDD3, TLCD4-RWDD3 (D46E +1 more)	Single nucleotide variant (3 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 2621942	NM_015485.5(RWDD3):c.172C>T (p.Pro58Ser)	RWDD3, TLCD4-RWDD3 (P58S +1 more)	Single nucleotide variant (3 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 2619820	NM_015485.5(RWDD3):c.391A>G (p.Thr131Ala)	RWDD3, TLCD4-RWDD3 (T131A +1 more)	Single nucleotide variant (3 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 2559838	NM_015485.5(RWDD3):c.403A>G (p.Met135Val)	RWDD3, TLCD4-RWDD3 (M120V +1 more)	Single nucleotide variant (3 prime UTR variant +2 more)	not specified	GLikely benign
Select item 2516088	NM_015485.5(RWDD3):c.26T>G (p.Leu9Arg)	LOC129930992, RWDD3 +1 more (L9R)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance
Select item 2485055	NM_015485.5(RWDD3):c.220C>A (p.Gln74Lys)	RWDD3, TLCD4-RWDD3 (Q74K +1 more)	Single nucleotide variant (3 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 2401433	NM_015485.5(RWDD3):c.149C>A (p.Pro50His)	RWDD3, TLCD4-RWDD3 (P35H +1 more)	Single nucleotide variant (3 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 2244397	NM_015485.5(RWDD3):c.451G>A (p.Ala151Thr)	RWDD3, TLCD4-RWDD3 (A136T +1 more)	Single nucleotide variant (3 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 2235326	NM_015485.5(RWDD3):c.206C>G (p.Ser69Trp)	RWDD3, TLCD4-RWDD3 (S54W +1 more)	Single nucleotide variant (3 prime UTR variant +2 more)	not specified	GUncertain significance