"Ambry Genetics"[submitter] AND "GSK3A"[gene] - ClinVar - NCBI

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Items: 13

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2396580	NM_019884.3(GSK3A):c.1262C>A (p.Pro421His)	GSK3A (P421H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2305959	NM_019884.3(GSK3A):c.989T>G (p.Val330Gly)	GSK3A (V330G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2549779	NM_019884.3(GSK3A):c.937C>G (p.Leu313Val)	GSK3A (L313V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3102914	NM_019884.3(GSK3A):c.709T>C (p.Ser237Pro)	GSK3A (S237P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2395883	NM_019884.3(GSK3A):c.380A>G (p.Asn127Ser)	GSK3A (N127S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2235776	NM_019884.3(GSK3A):c.337C>T (p.Arg113Cys)	GSK3A (R113C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3102913	NM_019884.3(GSK3A):c.263C>T (p.Pro88Leu)	GSK3A, LOC130064563 (P88L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3102912	NM_019884.3(GSK3A):c.231C>G (p.Ser77Arg)	GSK3A, LOC130064563 (S77R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3102911	NM_019884.3(GSK3A):c.179T>G (p.Val60Gly)	GSK3A, LOC130064563 (V60G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2222874	NM_019884.3(GSK3A):c.167T>G (p.Met56Arg)	GSK3A, LOC130064563 (M56R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2226744	NM_019884.3(GSK3A):c.158T>G (p.Val53Gly)	GSK3A, LOC130064563 (V53G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3102910	NM_019884.3(GSK3A):c.142G>A (p.Gly48Ser)	GSK3A, LOC130064563 (G48S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2386707	NM_019884.3(GSK3A):c.124G>A (p.Gly42Ser)	GSK3A, LOC130064563 (G42S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance