ClinVar (all) for Orgtrack (Select 507187) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 694238	NM_001007228.2(SPOP):c.295C>T (p.Arg99Trp)	SPOP (R99W)	Single nucleotide variant (missense variant)	Neurodevelopmental disorder with relative macrocephaly and with or without cardiac or endocrine anomalies +1 more	GConflicting classifications of pathogenicity
Select item 694237	NM_001007228.2(SPOP):c.293T>A (p.Val98Asp)	SPOP (V98D)	Single nucleotide variant (missense variant)	Malignant tumor of prostate	GUncertain significance
Select item 694236	NM_001007228.2(SPOP):c.291A>G (p.Glu97=)	SPOP	Single nucleotide variant (synonymous variant)	Malignant tumor of prostate	GUncertain significance
Select item 694235	NM_001007228.2(SPOP):c.289G>A (p.Glu97Lys)	SPOP (E97K)	Single nucleotide variant (missense variant)	Malignant tumor of prostate	GUncertain significance
Select item 694234	NM_001007228.2(SPOP):c.288del (p.Ser96fs)	SPOP (S96fs)	Deletion (frameshift variant)	Malignant tumor of prostate	GUncertain significance
Select item 694233	NM_001007228.2(SPOP):c.287del (p.Ser96fs)	SPOP (S96fs)	Deletion (frameshift variant)	Malignant tumor of prostate	GUncertain significance
Select item 694232	NM_001007228.2(SPOP):c.285dup (p.Ser96fs)	SPOP (S96fs)	Duplication (frameshift variant)	Malignant tumor of prostate	GUncertain significance
Select item 694231	NM_001007228.2(SPOP):c.284del (p.Lys95fs)	SPOP (K95fs)	Deletion (frameshift variant)	Malignant tumor of prostate	GUncertain significance
Select item 694230	NM_001007228.2(SPOP):c.282_283insC (p.Lys95fs)	SPOP (K95fs)	Insertion (frameshift variant)	Malignant tumor of prostate	GUncertain significance
Select item 694229	NM_001007228.2(SPOP):c.281del (p.Pro94fs)	SPOP (P94fs)	Deletion (frameshift variant)	Malignant tumor of prostate	GUncertain significance
Select item 694228	NM_001007228.2(SPOP):c.280C>T (p.Pro94Ser)	SPOP (P94S)	Single nucleotide variant (missense variant)	Malignant tumor of prostate	GUncertain significance
Select item 694227	NM_001007228.2(SPOP):c.278del (p.Cys93fs)	SPOP (C93fs)	Deletion (frameshift variant)	Malignant tumor of prostate	GUncertain significance
Select item 694226	NM_001007228.2(SPOP):c.276dup (p.Cys93fs)	SPOP (C93fs)	Duplication (frameshift variant)	Malignant tumor of prostate	GUncertain significance
Select item 694225	NM_001007228.2(SPOP):c.274del (p.Ser92fs)	SPOP (S92fs)	Deletion (frameshift variant)	Malignant tumor of prostate	GUncertain significance
Select item 694224	NM_001007228.2(SPOP):c.273del (p.Ser92fs)	SPOP (S92fs)	Deletion (frameshift variant)	Malignant tumor of prostate	GUncertain significance
Select item 694223	NM_001007228.2(SPOP):c.273C>T (p.Val91=)	SPOP	Single nucleotide variant (synonymous variant)	Malignant tumor of prostate	GUncertain significance
Select item 694222	NM_001007228.2(SPOP):c.272dup (p.Ser92fs)	SPOP (S92fs)	Duplication (frameshift variant)	Malignant tumor of prostate	GUncertain significance
Select item 694221	NM_001007228.2(SPOP):c.269del (p.Leu90fs)	SPOP (L90fs)	Deletion (frameshift variant)	Malignant tumor of prostate	GUncertain significance
Select item 694220	NM_001007228.2(SPOP):c.267A>G (p.Leu89=)	SPOP	Single nucleotide variant (synonymous variant)	Malignant tumor of prostate	GUncertain significance
Select item 694219	NM_001007228.2(SPOP):c.266T>G (p.Leu89Ter)	SPOP (L89*)	Single nucleotide variant (nonsense)	Malignant tumor of prostate	GUncertain significance
Select item 694218	NM_001007228.2(SPOP):c.266del (p.Leu89fs)	SPOP (L89fs)	Deletion (frameshift variant)	Malignant tumor of prostate	GUncertain significance
Select item 694217	NM_001007228.2(SPOP):c.263T>A (p.Leu88Gln)	SPOP (L88Q)	Single nucleotide variant (missense variant)	Malignant tumor of prostate	GUncertain significance
Select item 694216	NM_001007228.2(SPOP):c.260del (p.Tyr87fs)	SPOP (Y87fs)	Deletion (frameshift variant)	Malignant tumor of prostate	GUncertain significance
Select item 694215	NM_001007228.2(SPOP):c.260dup (p.Tyr87Ter)	SPOP (Y87*)	Duplication (nonsense)	Malignant tumor of prostate	GUncertain significance
Select item 694214	NM_001007228.2(SPOP):c.210A>T (p.Arg70=)	SPOP	Single nucleotide variant (synonymous variant)	Malignant tumor of prostate	GUncertain significance
Select item 694213	NM_001007228.2(SPOP):c.209G>C (p.Arg70Pro)	SPOP (R70P)	Single nucleotide variant (missense variant)	Malignant tumor of prostate	GUncertain significance
Select item 694212	NM_001007228.2(SPOP):c.206_207insTC (p.Leu69fs)	SPOP (L69fs)	Insertion (frameshift variant)	Malignant tumor of prostate	GUncertain significance
Select item 694211	NM_001007228.2(SPOP):c.201-2A>G	SPOP	Single nucleotide variant (splice acceptor variant)	Malignant tumor of prostate	GUncertain significance
Select item 694210	NM_001007228.2(SPOP):c.201-1G>C	SPOP	Single nucleotide variant (splice acceptor variant)	Malignant tumor of prostate	GUncertain significance
Select item 694209	NM_001007228.2(SPOP):c.201-10_201-9insA	SPOP	Insertion (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 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 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 694199	NM_001007228.2(SPOP):c.478G>A (p.Glu160Lys)	SPOP (E160K)	Single nucleotide variant (missense variant)	Neurodevelopmental disorder with microcephaly and dysmorphic facies +1 more	GConflicting classifications of pathogenicity
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 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 694190	NM_001007228.2(SPOP):c.416del (p.Arg139fs)	SPOP (R139fs)	Deletion (frameshift 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 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 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
Select item 694157	NM_001007228.2(SPOP):c.317T>C (p.Ile106Thr)	SPOP (I106T)	Single nucleotide variant (missense variant)	Malignant tumor of prostate	GUncertain significance
Select item 694156	NM_001007228.2(SPOP):c.316del (p.Ile106fs)	SPOP (I106fs)	Deletion (frameshift variant)	Malignant tumor of prostate	GUncertain significance
Select item 694155	NM_001007228.2(SPOP):c.315del (p.Ile106fs)	SPOP (I106fs)	Deletion (frameshift variant)	Malignant tumor of prostate	GUncertain significance
Select item 694154	NM_001007228.2(SPOP):c.309del (p.Lys103fs)	SPOP (K103fs)	Deletion (frameshift variant)	Malignant tumor of prostate	GUncertain significance
Select item 694153	NM_001007228.2(SPOP):c.308A>C (p.Lys103Thr)	SPOP (K103T)	Single nucleotide variant (missense variant)	Malignant tumor of prostate	GUncertain significance
Select item 694152	NM_001007228.2(SPOP):c.297_298insA (p.Ala100fs)	SPOP (A100fs)	Insertion (frameshift variant)	Malignant tumor of prostate	GUncertain significance
Select item 694151	NM_001007228.2(SPOP):c.259T>G (p.Tyr87Asp)	SPOP (Y87D)	Single nucleotide variant (missense variant)	Malignant tumor of prostate	GUncertain significance
Select item 694150	NM_001007228.2(SPOP):c.259dup (p.Tyr87fs)	SPOP (Y87fs)	Duplication (frameshift variant)	Malignant tumor of prostate	GUncertain significance
Select item 694149	NM_001007228.2(SPOP):c.258T>C (p.Leu86=)	SPOP	Single nucleotide variant (synonymous variant)	Malignant tumor of prostate	GUncertain significance
Select item 694148	NM_001007228.2(SPOP):c.255del (p.Leu86fs)	SPOP (L86fs)	Deletion (frameshift variant)	Malignant tumor of prostate	GUncertain significance
Select item 694147	NM_001007228.2(SPOP):c.255A>T (p.Ser85=)	SPOP	Single nucleotide variant (synonymous variant)	Malignant tumor of prostate	GUncertain significance
Select item 694146	NM_001007228.2(SPOP):c.255dup (p.Leu86fs)	SPOP (L86fs)	Duplication (frameshift variant)	Malignant tumor of prostate	GUncertain significance
Select item 694145	NM_001007228.2(SPOP):c.254del (p.Ser85fs)	SPOP (S85fs)	Deletion (frameshift variant)	Malignant tumor of prostate	GUncertain significance
Select item 694144	NM_001007228.2(SPOP):c.254dup (p.Leu86fs)	SPOP (L86fs)	Duplication (frameshift variant)	Malignant tumor of prostate	GUncertain significance
Select item 694143	NM_001007228.2(SPOP):c.252del (p.Ser85fs)	SPOP (S85fs)	Deletion (frameshift variant)	Malignant tumor of prostate	GUncertain significance
Select item 694142	NM_001007228.2(SPOP):c.251delinsGG (p.Leu84fs)	SPOP (L84fs)	Indel (frameshift variant)	Malignant tumor of prostate	GUncertain significance
Select item 694141	NM_001007228.2(SPOP):c.250C>T (p.Leu84=)	SPOP	Single nucleotide variant (synonymous variant)	Malignant tumor of prostate	GUncertain significance
Select item 694140	NM_001007228.2(SPOP):c.247del (p.Tyr83fs)	SPOP (Y83fs)	Deletion (frameshift variant)	Malignant tumor of prostate	GUncertain significance
Select item 694139	NM_001007228.2(SPOP):c.246T>A (p.Asp82Glu)	SPOP (D82E)	Single nucleotide variant (missense variant)	Malignant tumor of prostate	GUncertain significance

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