Related gene-specific medical variations for Gene (Select 150290) - ClinVar - NCBI

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Items: 19

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3274053	NM_152511.5(DUSP18):c.199A>G (p.Met67Val)	DUSP18, SLC35E4 (M67V)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 3274052	NM_152511.5(DUSP18):c.152A>G (p.Asn51Ser)	DUSP18, SLC35E4 (N51S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3086286	NM_152511.5(DUSP18):c.412C>T (p.Arg138Trp)	DUSP18, SLC35E4 (R138W +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3086285	NM_152511.5(DUSP18):c.232C>T (p.Arg78Cys)	DUSP18, SLC35E4 (R78C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2600451	NM_152511.5(DUSP18):c.17G>A (p.Cys6Tyr)	DUSP18, SLC35E4 (C6Y)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2522497	NM_152511.5(DUSP18):c.134A>G (p.Gln45Arg)	DUSP18, SLC35E4 (Q45R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2511008	NM_152511.5(DUSP18):c.302T>G (p.Leu101Trp)	DUSP18, SLC35E4 (L101W +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2458664	NM_152511.5(DUSP18):c.221C>T (p.Ser74Phe)	DUSP18, SLC35E4 (S74F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2411946	NM_152511.5(DUSP18):c.533A>G (p.Tyr178Cys)	DUSP18, SLC35E4 (Y178C)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2398268	NM_152511.5(DUSP18):c.487A>G (p.Thr163Ala)	DUSP18, SLC35E4 (T163A)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2364191	NM_152511.5(DUSP18):c.37C>T (p.Arg13Trp)	DUSP18, SLC35E4 (R13W)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2357904	NM_152511.5(DUSP18):c.296G>A (p.Arg99His)	DUSP18, SLC35E4 (R99H)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2344377	NM_152511.5(DUSP18):c.493C>T (p.His165Tyr)	DUSP18, SLC35E4 (H165Y)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2342867	NM_152511.5(DUSP18):c.547C>T (p.Arg183Cys)	DUSP18, SLC35E4 (R183C)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2332467	NM_152511.5(DUSP18):c.563T>C (p.Leu188Pro)	DUSP18, SLC35E4 (L188P)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2324253	NM_152511.5(DUSP18):c.202C>G (p.Gln68Glu)	DUSP18, SLC35E4 (Q68E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2322025	NM_152511.5(DUSP18):c.425G>A (p.Arg142Gln)	DUSP18, SLC35E4 (R142Q)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2294449	NM_152511.5(DUSP18):c.235C>G (p.Leu79Val)	DUSP18, SLC35E4 (L79V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2247176	NM_152511.5(DUSP18):c.14C>T (p.Ser5Leu)	DUSP18, SLC35E4 (S5L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance