Related gene-specific medical variations for Gene (Select 373156) - ClinVar - NCBI

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Items: 19

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3283016	NM_015917.3(GSTK1):c.620C>T (p.Ala207Val)	GSTK1, TMEM139-AS1 (A263V +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3283015	NM_015917.3(GSTK1):c.607A>C (p.Met203Leu)	GSTK1, TMEM139-AS1 (M191L +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3102975	NM_015917.3(GSTK1):c.437G>A (p.Gly146Asp)	GSTK1, TMEM139-AS1 (G134D +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3102974	NM_015917.3(GSTK1):c.350C>T (p.Ala117Val)	GSTK1, TMEM139-AS1 (A117V +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3102973	NM_015917.3(GSTK1):c.313G>A (p.Ala105Thr)	GSTK1, TMEM139-AS1 (A105T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3102972	NM_015917.3(GSTK1):c.203A>G (p.Asn68Ser)	GSTK1, TMEM139-AS1 (N68S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3102971	NM_015917.3(GSTK1):c.13C>T (p.Pro5Ser)	GSTK1, LOC113687200 +1 more (P5S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2599508	NM_015917.3(GSTK1):c.193T>C (p.Tyr65His)	GSTK1, TMEM139-AS1 (Y65H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2549525	NM_015917.3(GSTK1):c.664G>A (p.Val222Met)	GSTK1, TMEM139-AS1 (V179M +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2511336	NM_015917.3(GSTK1):c.349G>C (p.Ala117Pro)	GSTK1, TMEM139-AS1 (A74P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2494387	NM_015917.3(GSTK1):c.385-36C>G	GSTK1, TMEM139-AS1 (P173A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2483076	NM_015917.3(GSTK1):c.17G>C (p.Arg6Pro)	GSTK1, LOC113687200 +1 more (R6P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2371475	NM_015917.3(GSTK1):c.291G>T (p.Leu97Phe)	GSTK1, TMEM139-AS1 (L97F +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2309543	NM_015917.3(GSTK1):c.20C>T (p.Thr7Ile)	GSTK1, LOC113687200 +1 more (T7I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2238993	NM_015917.3(GSTK1):c.181C>T (p.Arg61Cys)	GSTK1, TMEM139-AS1 (R61C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2224927	NM_015917.3(GSTK1):c.60G>T (p.Trp20Cys)	GSTK1, LOC113687200 +1 more (W20C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 776267	NM_015917.3(GSTK1):c.632-4C>G	GSTK1, TMEM139-AS1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 726354	NM_015917.3(GSTK1):c.558C>T (p.Thr186=)	GSTK1, TMEM139-AS1	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 708871	NM_015917.3(GSTK1):c.382A>G (p.Arg128Gly)	TMEM139-AS1, GSTK1 (R128G +1 more)	Single nucleotide variant (missense variant)	not provided	GLikely benign