Related gene-specific medical variations for Gene (Select 26168) - ClinVar

Warning: The NCBI web site requires JavaScript to function. more...

Links from Gene

Items: 29

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3317437	NM_015670.6(SENP3):c.788C>T (p.Pro263Leu)	SENP3, SENP3-EIF4A1 (P263L)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3317435	NM_015670.6(SENP3):c.1670C>A (p.Pro557His)	SENP3, SENP3-EIF4A1 (P557H)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3317434	NM_015670.6(SENP3):c.712T>G (p.Ser238Ala)	SENP3, SENP3-EIF4A1 (S238A)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3317433	NM_015670.6(SENP3):c.538C>T (p.Pro180Ser)	SENP3, SENP3-EIF4A1 (P180S)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3317432	NM_015670.6(SENP3):c.910G>A (p.Gly304Ser)	SENP3, SENP3-EIF4A1 (G304S)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3159961	NM_015670.6(SENP3):c.908C>T (p.Ala303Val)	SENP3, SENP3-EIF4A1 (A303V)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3159960	NM_015670.6(SENP3):c.828C>T (p.Ile276=)	SENP3, SENP3-EIF4A1	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GLikely benign
Select item 3159959	NM_015670.6(SENP3):c.79C>G (p.Pro27Ala)	SENP3, SENP3-EIF4A1 (P27A)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3159958	NM_015670.6(SENP3):c.716G>A (p.Gly239Asp)	SENP3, SENP3-EIF4A1 (G239D)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3159957	NM_015670.6(SENP3):c.670G>T (p.Asp224Tyr)	SENP3, SENP3-EIF4A1 (D224Y)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3159956	NM_015670.6(SENP3):c.628A>G (p.Arg210Gly)	SENP3, SENP3-EIF4A1 (R210G)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3159955	NM_015670.6(SENP3):c.262G>A (p.Asp88Asn)	SENP3, SENP3-EIF4A1 (D88N)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2604858	NM_015670.6(SENP3):c.1144G>T (p.Ala382Ser)	SENP3, SENP3-EIF4A1 (A382S)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2568732	NM_015670.6(SENP3):c.255G>C (p.Glu85Asp)	SENP3, SENP3-EIF4A1 (E85D)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2528573	NM_015670.6(SENP3):c.229G>A (p.Glu77Lys)	SENP3, SENP3-EIF4A1 (E77K)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2488415	NM_015670.6(SENP3):c.559G>C (p.Asp187His)	SENP3, SENP3-EIF4A1 (D187H)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2395558	NM_015670.6(SENP3):c.772G>C (p.Glu258Gln)	SENP3, SENP3-EIF4A1 (E258Q)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2390386	NM_015670.6(SENP3):c.409C>T (p.Leu137Phe)	SENP3, SENP3-EIF4A1 (L137F)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2355307	NM_015670.6(SENP3):c.301A>G (p.Arg101Gly)	SENP3, SENP3-EIF4A1 (R101G)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2293184	NM_015670.6(SENP3):c.354T>A (p.His118Gln)	SENP3, SENP3-EIF4A1 (H118Q)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2291825	NM_015670.6(SENP3):c.787C>A (p.Pro263Thr)	SENP3, SENP3-EIF4A1 (P263T)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2275935	NM_015670.6(SENP3):c.980C>G (p.Thr327Arg)	SENP3, SENP3-EIF4A1 (T327R)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2265274	NM_015670.6(SENP3):c.686C>T (p.Thr229Ile)	SENP3, SENP3-EIF4A1 (T229I)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2250516	NM_015670.6(SENP3):c.655C>T (p.Pro219Ser)	SENP3, SENP3-EIF4A1 (P219S)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2226774	NM_015670.6(SENP3):c.742G>C (p.Gly248Arg)	SENP3, SENP3-EIF4A1 (G248R)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2223949	NM_015670.6(SENP3):c.818T>C (p.Val273Ala)	SENP3, SENP3-EIF4A1 (V273A)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2218950	NM_015670.6(SENP3):c.470G>A (p.Arg157Gln)	SENP3, SENP3-EIF4A1 (R157Q)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2209762	NM_015670.6(SENP3):c.91C>T (p.Arg31Cys)	SENP3, SENP3-EIF4A1 (R31C)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 1801810	NM_015670.6(SENP3):c.1544G>T (p.Trp515Leu)	SENP3, SENP3-EIF4A1 (W515L)	Single nucleotide variant (non-coding transcript variant +1 more)	Myoepithelial tumor	GUncertain significance

ClinVar

Result Filters

Classification type

Germline classification

Types of conflicts

Molecular consequence

Variation type

Variation size

Variant length

Review status

Additional filters

Links from Gene

Items: 29