C0376358[trait identifier] AND "Laboratory of Virology, Microbiology, - ClinVar - NCBI

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

Search results

Items: 1 to 100 of 160

<< First< Prev

Page of 2

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 694202	NM_001007228.2(SPOP):c.480+1071G>T	SPOP	Single nucleotide variant (intron variant)	Malignant tumor of prostate	GUncertain significance
Select item 694201	NM_001007228.2(SPOP):c.480+1065A>G	SPOP	Single nucleotide variant (intron variant)	Malignant tumor of prostate	GUncertain significance
Select item 694200	NM_001007228.2(SPOP):c.480+1059A>G	SPOP	Single nucleotide variant (intron variant)	Malignant tumor of prostate	GUncertain significance
Select item 694207	NM_001007228.2(SPOP):c.480+51T>G	SPOP	Single nucleotide variant (intron variant)	Malignant tumor of prostate	GUncertain significance
Select item 694206	NM_001007228.2(SPOP):c.480+39A>T	SPOP	Single nucleotide variant (intron variant)	Malignant tumor of prostate	GUncertain significance
Select item 694205	NM_001007228.2(SPOP):c.480+38G>A	SPOP	Single nucleotide variant (intron variant)	Malignant tumor of prostate	GUncertain significance
Select item 694204	NM_001007228.2(SPOP):c.480+28G>C	SPOP	Single nucleotide variant (intron variant)	Malignant tumor of prostate	GUncertain significance
Select item 694203	NM_001007228.2(SPOP):c.480+17T>G	SPOP	Single nucleotide variant (intron variant)	Malignant tumor of prostate	GUncertain significance
Select item 694208	NM_001007228.2(SPOP):c.480+5G>T	SPOP	Single nucleotide variant (intron variant)	Malignant tumor of prostate	GUncertain significance
Select item 694199	NM_001007228.2(SPOP):c.478G>A (p.Glu160Lys)	SPOP (E160K)	Single nucleotide variant (missense variant)	Neurodevelopmental disorder with microcephaly and dysmorphic facies	GPathogenic
Select item 694198	NM_001007228.2(SPOP):c.475del (p.Cys159fs)	SPOP (C159fs)	Deletion (frameshift variant)	Malignant tumor of prostate	GUncertain significance
Select item 694197	NM_001007228.2(SPOP):c.474del (p.Cys159fs)	SPOP (C159fs)	Deletion (frameshift variant)	Malignant tumor of prostate	GUncertain significance
Select item 694196	NM_001007228.2(SPOP):c.474C>G (p.Phe158Leu)	SPOP (F158L)	Single nucleotide variant (missense variant)	Malignant tumor of prostate	GUncertain significance
Select item 694082	NM_001007228.2(SPOP):c.474C>A (p.Phe158Leu)	SPOP (F158L)	Single nucleotide variant (missense variant)	Malignant tumor of prostate	GUncertain significance
Select item 694195	NM_001007228.2(SPOP):c.473T>G (p.Phe158Cys)	SPOP (F158C)	Single nucleotide variant (missense variant)	Malignant tumor of prostate	GUncertain significance
Select item 694194	NM_001007228.2(SPOP):c.473T>A (p.Phe158Tyr)	SPOP (F158Y)	Single nucleotide variant (missense variant)	Malignant tumor of prostate	GUncertain significance
Select item 694193	NM_001007228.2(SPOP):c.472T>C (p.Phe158Leu)	SPOP (F158L)	Single nucleotide variant (missense variant)	Malignant tumor of prostate	GUncertain significance
Select item 694192	NM_001007228.2(SPOP):c.472T>A (p.Phe158Ile)	SPOP (F158I)	Single nucleotide variant (missense variant)	Malignant tumor of prostate	GUncertain significance
Select item 694191	NM_001007228.2(SPOP):c.470T>C (p.Leu157Pro)	SPOP (L157P)	Single nucleotide variant (missense variant)	Malignant tumor of prostate	GUncertain significance
Select item 694127	NM_001007228.2(SPOP):c.470del (p.Leu157fs)	SPOP (L157fs)	Deletion (frameshift variant)	Malignant tumor of prostate	GUncertain significance
Select item 694126	NM_001007228.2(SPOP):c.469del (p.Leu157fs)	SPOP (L157fs)	Deletion (frameshift variant)	Malignant tumor of prostate	GUncertain significance
Select item 694125	NM_001007228.2(SPOP):c.469C>T (p.Leu157Phe)	SPOP (L157F)	Single nucleotide variant (missense variant)	Malignant tumor of prostate	GUncertain significance
Select item 694124	NM_001007228.2(SPOP):c.466A>T (p.Thr156Ser)	SPOP (T156S)	Single nucleotide variant (missense variant)	Malignant tumor of prostate	GUncertain significance
Select item 694123	NM_001007228.2(SPOP):c.466A>G (p.Thr156Ala)	SPOP (T156A)	Single nucleotide variant (missense variant)	Malignant tumor of prostate	GUncertain significance
Select item 694122	NM_001007228.2(SPOP):c.466A>C (p.Thr156Pro)	SPOP (T156P)	Single nucleotide variant (missense variant)	Malignant tumor of prostate	GUncertain significance
Select item 694121	NM_001007228.2(SPOP):c.464T>A (p.Leu155His)	SPOP (L155H)	Single nucleotide variant (missense variant)	Malignant tumor of prostate	GUncertain significance
Select item 694120	NM_001007228.2(SPOP):c.463C>T (p.Leu155Phe)	SPOP (L155F)	Single nucleotide variant (missense variant)	Malignant tumor of prostate	GUncertain significance
Select item 694119	NM_001007228.2(SPOP):c.457del (p.Asp153fs)	SPOP (D153fs)	Deletion (frameshift variant)	Malignant tumor of prostate	GUncertain significance
Select item 694118	NM_001007228.2(SPOP):c.456T>G (p.Asp152Glu)	SPOP (D152E)	Single nucleotide variant (missense variant)	Malignant tumor of prostate	GUncertain significance
Select item 694117	NM_001007228.2(SPOP):c.456T>A (p.Asp152Glu)	SPOP (D152E)	Single nucleotide variant (missense variant)	Malignant tumor of prostate	GUncertain significance
Select item 694116	NM_001007228.2(SPOP):c.456del (p.Asp152fs)	SPOP (D152fs)	Deletion (frameshift variant)	Malignant tumor of prostate	GUncertain significance
Select item 694115	NM_001007228.2(SPOP):c.454G>A (p.Asp152Asn)	SPOP (D152N)	Single nucleotide variant (missense variant)	Malignant tumor of prostate	GUncertain significance
Select item 694114	NM_001007228.2(SPOP):c.453T>G (p.Pro151=)	SPOP	Single nucleotide variant (synonymous variant)	Malignant tumor of prostate	GUncertain significance
Select item 694113	NM_001007228.2(SPOP):c.453del (p.Asp152fs)	SPOP (D152fs)	Deletion (frameshift variant)	Malignant tumor of prostate	GUncertain significance
Select item 694112	NM_001007228.2(SPOP):c.429_430insT (p.Asp144Ter)	SPOP (D144*)	Insertion (nonsense)	Malignant tumor of prostate	GUncertain significance
Select item 694111	NM_001007228.2(SPOP):c.429_430del (p.Leu143_Asp144insTer)	SPOP	Deletion (frameshift variant)	Malignant tumor of prostate	GUncertain significance
Select item 694110	NM_001007228.2(SPOP):c.428T>G (p.Leu143Trp)	SPOP (L143W)	Single nucleotide variant (missense variant)	Malignant tumor of prostate	GUncertain significance
Select item 694109	NM_001007228.2(SPOP):c.427T>A (p.Leu143Met)	SPOP (L143M)	Single nucleotide variant (missense variant)	Malignant tumor of prostate	GUncertain significance
Select item 694108	NM_001007228.2(SPOP):c.424C>T (p.Leu142Phe)	SPOP (L142F)	Single nucleotide variant (missense variant)	Malignant tumor of prostate	GUncertain significance
Select item 694107	NM_001007228.2(SPOP):c.420T>G (p.Asp140Glu)	SPOP (D140E)	Single nucleotide variant (missense variant)	Malignant tumor of prostate	GUncertain significance
Select item 694106	NM_001007228.2(SPOP):c.419A>C (p.Asp140Ala)	SPOP (D140A)	Single nucleotide variant (missense variant)	Malignant tumor of prostate	GUncertain significance
Select item 694105	NM_001007228.2(SPOP):c.418del (p.Asp140fs)	SPOP (D140fs)	Deletion (frameshift variant)	Malignant tumor of prostate	GUncertain significance
Select item 694190	NM_001007228.2(SPOP):c.416del (p.Arg139fs)	SPOP (R139fs)	Deletion (frameshift variant)	Malignant tumor of prostate	GUncertain significance
Select item 694104	NM_001007228.2(SPOP):c.416G>A (p.Arg139Lys)	SPOP (R139K)	Single nucleotide variant (missense variant)	Malignant tumor of prostate	GUncertain significance
Select item 694081	NM_001007228.2(SPOP):c.414T>G (p.Arg138=)	SPOP	Single nucleotide variant (synonymous variant)	Malignant tumor of prostate	GUncertain significance
Select item 694189	NM_001007228.2(SPOP):c.413G>A (p.Arg138His)	SPOP (R138H)	Single nucleotide variant (missense variant)	Malignant tumor of prostate	GUncertain significance
Select item 694188	NM_001007228.2(SPOP):c.408C>A (p.Phe136Leu)	SPOP (F136L)	Single nucleotide variant (missense variant)	Malignant tumor of prostate	GUncertain significance
Select item 694187	NM_001007228.2(SPOP):c.402dup (p.Lys135fs)	SPOP (K135fs)	Duplication (frameshift variant)	Malignant tumor of prostate	GUncertain significance
Select item 694186	NM_001007228.2(SPOP):c.401del (p.Lys134fs)	SPOP (K134fs)	Deletion (frameshift variant)	Malignant tumor of prostate	GUncertain significance
Select item 694185	NM_001007228.2(SPOP):c.401A>G (p.Lys134Arg)	SPOP (K134R)	Single nucleotide variant (missense variant)	Malignant tumor of prostate	GUncertain significance
Select item 694184	NM_001007228.2(SPOP):c.400A>C (p.Lys134Gln)	SPOP (K134Q)	Single nucleotide variant (missense variant)	Malignant tumor of prostate	GUncertain significance
Select item 694183	NM_001007228.2(SPOP):c.399del (p.Phe133fs)	SPOP (F133fs)	Deletion (frameshift variant)	Malignant tumor of prostate	GUncertain significance
Select item 694182	NM_001007228.2(SPOP):c.397T>C (p.Phe133Leu)	SPOP (F133L)	Single nucleotide variant (missense variant)	Malignant tumor of prostate	GUncertain significance
Select item 376548	NM_001007228.2(SPOP):c.397T>A (p.Phe133Ile)	SPOP (F133I)	Single nucleotide variant (missense variant)	Prostate adenocarcinoma +1 more	GConflicting classifications of pathogenicity
Select item 376545	NM_001007228.2(SPOP):c.397T>G (p.Phe133Val)	SPOP (F133V)	Single nucleotide variant (missense variant)	Prostate adenocarcinoma +1 more	GConflicting classifications of pathogenicity
Select item 694181	NM_001007228.2(SPOP):c.388G>T (p.Asp130Tyr)	SPOP (D130Y)	Single nucleotide variant (missense variant)	Malignant tumor of prostate	GUncertain significance
Select item 694180	NM_001007228.2(SPOP):c.388G>A (p.Asp130Asn)	SPOP (D130N)	Single nucleotide variant (missense variant)	Malignant tumor of prostate	GUncertain significance
Select item 694179	NM_001007228.2(SPOP):c.386A>C (p.Lys129Thr)	SPOP (K129T)	Single nucleotide variant (missense variant)	Malignant tumor of prostate	GUncertain significance
Select item 694178	NM_001007228.2(SPOP):c.384del (p.Asp130fs)	SPOP (D130fs)	Deletion (frameshift variant)	Malignant tumor of prostate	GUncertain significance
Select item 694177	NM_001007228.2(SPOP):c.384C>T (p.Gly128=)	SPOP	Single nucleotide variant (synonymous variant)	Malignant tumor of prostate	GUncertain significance
Select item 694176	NM_001007228.2(SPOP):c.384C>G (p.Gly128=)	SPOP	Single nucleotide variant (synonymous variant)	Malignant tumor of prostate	GUncertain significance
Select item 694175	NM_001007228.2(SPOP):c.384C>A (p.Gly128=)	SPOP	Single nucleotide variant (synonymous variant)	Malignant tumor of prostate	GUncertain significance
Select item 694174	NM_001007228.2(SPOP):c.381A>G (p.Gln127=)	SPOP	Single nucleotide variant (synonymous variant)	Malignant tumor of prostate	GUncertain significance
Select item 694173	NM_001007228.2(SPOP):c.377T>G (p.Val126Gly)	SPOP (V126G)	Single nucleotide variant (missense variant)	Malignant tumor of prostate	GUncertain significance
Select item 694172	NM_001007228.2(SPOP):c.375T>A (p.Phe125Leu)	SPOP (F125L)	Single nucleotide variant (missense variant)	Malignant tumor of prostate	GUncertain significance
Select item 694171	NM_001007228.2(SPOP):c.373T>C (p.Phe125Leu)	SPOP (F125L)	Single nucleotide variant (missense variant)	Malignant tumor of prostate	GUncertain significance
Select item 694170	NM_001007228.2(SPOP):c.366A>C (p.Ala122=)	SPOP	Single nucleotide variant (synonymous variant)	Malignant tumor of prostate	GUncertain significance
Select item 694169	NM_001007228.2(SPOP):c.365C>A (p.Ala122Glu)	SPOP (A122E)	Single nucleotide variant (missense variant)	Malignant tumor of prostate	GUncertain significance
Select item 694168	NM_001007228.2(SPOP):c.361C>T (p.Arg121Trp)	SPOP (R121W)	Single nucleotide variant (missense variant)	Malignant tumor of prostate	GUncertain significance
Select item 694103	NM_001007228.2(SPOP):c.360del (p.Gln120fs)	SPOP (Q120fs)	Deletion (frameshift variant)	Malignant tumor of prostate	GUncertain significance
Select item 694102	NM_001007228.2(SPOP):c.358del (p.Gln120fs)	SPOP (Q120fs)	Deletion (frameshift variant)	Malignant tumor of prostate	GUncertain significance
Select item 694100	NM_001007228.2(SPOP):c.355dup (p.Ser119fs)	SPOP (S119fs)	Duplication (frameshift variant)	Malignant tumor of prostate	GUncertain significance
Select item 694101	NM_001007228.2(SPOP):c.355del (p.Ser119fs)	SPOP (S119fs)	Deletion (frameshift variant)	Malignant tumor of prostate	GUncertain significance
Select item 694099	NM_001007228.2(SPOP):c.354G>A (p.Glu118=)	SPOP	Single nucleotide variant (synonymous variant)	Malignant tumor of prostate	GUncertain significance
Select item 694098	NM_001007228.2(SPOP):c.354del (p.Ser119fs)	SPOP (S119fs)	Deletion (frameshift variant)	Malignant tumor of prostate	GUncertain significance
Select item 694089	NM_001007228.2(SPOP):c.353-1G>T	SPOP	Single nucleotide variant (splice acceptor variant)	Malignant tumor of prostate	GUncertain significance
Select item 694088	NM_001007228.2(SPOP):c.353-1G>A	SPOP	Single nucleotide variant (splice acceptor variant)	not provided	GUncertain significance
Select item 694087	NM_001007228.2(SPOP):c.353-1del	SPOP	Deletion (splice acceptor variant)	Malignant tumor of prostate	GUncertain significance
Select item 694097	NM_001007228.2(SPOP):c.353-7A>C	SPOP	Single nucleotide variant (intron variant)	Malignant tumor of prostate	GUncertain significance
Select item 694083	NM_001007228.2(SPOP):c.353-11C>T	SPOP	Single nucleotide variant (intron variant)	Malignant tumor of prostate	GUncertain significance
Select item 694085	NM_001007228.2(SPOP):c.353-17T>G	SPOP	Single nucleotide variant (intron variant)	Malignant tumor of prostate	GUncertain significance
Select item 694084	NM_001007228.2(SPOP):c.353-17T>A	SPOP	Single nucleotide variant (intron variant)	Malignant tumor of prostate	GUncertain significance
Select item 694086	NM_001007228.2(SPOP):c.353-19T>G	SPOP	Single nucleotide variant (intron variant)	Malignant tumor of prostate	GUncertain significance
Select item 694091	NM_001007228.2(SPOP):c.353-21C>G	SPOP	Single nucleotide variant (intron variant)	Malignant tumor of prostate	GUncertain significance
Select item 694090	NM_001007228.2(SPOP):c.353-21C>A	SPOP	Single nucleotide variant (intron variant)	Malignant tumor of prostate	GUncertain significance
Select item 694092	NM_001007228.2(SPOP):c.353-32C>T	SPOP	Single nucleotide variant (intron variant)	Malignant tumor of prostate	GUncertain significance
Select item 694093	NM_001007228.2(SPOP):c.353-38C>G	SPOP	Single nucleotide variant (intron variant)	Malignant tumor of prostate	GUncertain significance
Select item 694094	NM_001007228.2(SPOP):c.353-39G>T	SPOP	Single nucleotide variant (intron variant)	Malignant tumor of prostate	GUncertain significance
Select item 694095	NM_001007228.2(SPOP):c.353-48C>A	SPOP	Single nucleotide variant (intron variant)	Malignant tumor of prostate	GUncertain significance
Select item 694096	NM_001007228.2(SPOP):c.353-51G>T	SPOP	Single nucleotide variant (intron variant)	Malignant tumor of prostate	GUncertain significance
Select item 694167	NM_001007228.2(SPOP):c.346G>C (p.Ala116Pro)	SPOP (A116P)	Single nucleotide variant (missense variant)	Malignant tumor of prostate	GUncertain significance
Select item 694166	NM_001007228.2(SPOP):c.346G>A (p.Ala116Thr)	SPOP (A116T)	Single nucleotide variant (missense variant)	Malignant tumor of prostate	GUncertain significance
Select item 694165	NM_001007228.2(SPOP):c.343A>T (p.Lys115Ter)	SPOP (K115*)	Single nucleotide variant (nonsense)	Malignant tumor of prostate	GUncertain significance
Select item 694164	NM_001007228.2(SPOP):c.342C>G (p.Thr114=)	SPOP	Single nucleotide variant (synonymous variant)	Malignant tumor of prostate	GUncertain significance
Select item 694163	NM_001007228.2(SPOP):c.337G>C (p.Glu113Gln)	SPOP (E113Q)	Single nucleotide variant (missense variant)	Malignant tumor of prostate	GUncertain significance
Select item 694162	NM_001007228.2(SPOP):c.337G>A (p.Glu113Lys)	SPOP (E113K)	Single nucleotide variant (missense variant)	Malignant tumor of prostate	GUncertain significance
Select item 694161	NM_001007228.2(SPOP):c.334G>A (p.Glu112Lys)	SPOP (E112K)	Single nucleotide variant (missense variant)	Malignant tumor of prostate	GUncertain significance
Select item 694160	NM_001007228.2(SPOP):c.327C>T (p.Ala109=)	SPOP	Single nucleotide variant (synonymous variant)	Malignant tumor of prostate	GUncertain significance
Select item 694159	NM_001007228.2(SPOP):c.325G>T (p.Ala109Ser)	SPOP (A109S)	Single nucleotide variant (missense variant)	Malignant tumor of prostate	GUncertain significance
Select item 694158	NM_001007228.2(SPOP):c.321dup (p.Asn108fs)	SPOP (N108fs)	Duplication (frameshift variant)	Malignant tumor of prostate	GUncertain significance

<< First< Prev

Page of 2