"Ambry Genetics"[submitter] AND "SENP5"[gene] - ClinVar

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Items: 29

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2358548	NM_152699.5(SENP5):c.41A>C (p.His14Pro)	SENP5 (H14P)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2289714	NM_152699.5(SENP5):c.206C>T (p.Thr69Met)	SENP5 (T69M)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2570473	NM_152699.5(SENP5):c.301G>A (p.Ala101Thr)	SENP5 (A101T)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GLikely benign
Select item 2589905	NM_152699.5(SENP5):c.335T>G (p.Leu112Arg)	SENP5 (L112R)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2325909	NM_152699.5(SENP5):c.356T>C (p.Leu119Pro)	SENP5 (L119P)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2316308	NM_152699.5(SENP5):c.437A>G (p.Asn146Ser)	SENP5 (N146S)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2313170	NM_152699.5(SENP5):c.457A>C (p.Asn153His)	SENP5 (N153H)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2285518	NM_152699.5(SENP5):c.482C>T (p.Pro161Leu)	SENP5 (P161L)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2607855	NM_152699.5(SENP5):c.502A>T (p.Met168Leu)	SENP5 (M168L)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2345716	NM_152699.5(SENP5):c.512A>G (p.Asn171Ser)	SENP5 (N171S)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2518751	NM_152699.5(SENP5):c.592G>A (p.Gly198Ser)	SENP5 (G198S)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2493828	NM_152699.5(SENP5):c.625G>C (p.Gly209Arg)	SENP5 (G209R)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2380101	NM_152699.5(SENP5):c.847G>A (p.Gly283Ser)	SENP5 (G283S)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2324500	NM_152699.5(SENP5):c.889A>G (p.Lys297Glu)	SENP5 (K297E)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2515399	NM_152699.5(SENP5):c.904C>T (p.Arg302Trp)	SENP5 (R302W)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2330364	NM_152699.5(SENP5):c.904C>G (p.Arg302Gly)	SENP5 (R302G)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2362591	NM_152699.5(SENP5):c.977G>C (p.Cys326Ser)	SENP5 (C326S)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2227903	NM_152699.5(SENP5):c.992G>A (p.Ser331Asn)	SENP5 (S331N)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2278630	NM_152699.5(SENP5):c.1138C>T (p.His380Tyr)	SENP5 (H380Y)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2251747	NM_152699.5(SENP5):c.1153A>G (p.Met385Val)	SENP5 (M385V)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2249683	NM_152699.5(SENP5):c.1163C>T (p.Ser388Leu)	SENP5 (S388L)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2324499	NM_152699.5(SENP5):c.1207A>T (p.Thr403Ser)	SENP5 (T403S)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2388835	NM_152699.5(SENP5):c.1264G>A (p.Val422Met)	SENP5 (V422M)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2565169	NM_152699.5(SENP5):c.1265T>G (p.Val422Gly)	SENP5 (V422G)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2246550	NM_152699.5(SENP5):c.1296G>C (p.Lys432Asn)	SENP5 (K432N)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2517946	NM_152699.5(SENP5):c.1381C>G (p.Pro461Ala)	SENP5 (P461A)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2314933	NM_152699.5(SENP5):c.1583G>A (p.Arg528Lys)	SENP5 (R528K)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2407662	NM_152699.5(SENP5):c.2121G>C (p.Gln707His)	SENP5 (Q707H +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2394639	NM_152699.5(SENP5):c.2125A>C (p.Asn709His)	SENP5 (N663H +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance

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Items: 29