"Labcorp Genetics (formerly Invitae), Labcorp"[submitter] AND "TAB2"[g - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2025560	NM_001292034.3(TAB2):c.10G>A (p.Gly4Arg)	TAB2 (G4R)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2976031	NM_001292034.3(TAB2):c.18C>T (p.His6=)	TAB2	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 1540615	NM_001292034.3(TAB2):c.21A>G (p.Gln7=)	TAB2	Single nucleotide variant (synonymous variant +1 more)	not provided +1 more	GBenign/Likely benign
Select item 1908034	NM_001292034.3(TAB2):c.25G>A (p.Asp9Asn)	TAB2 (D9N)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2756093	NM_001292034.3(TAB2):c.89G>A (p.Arg30Lys)	TAB2 (R30K)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2957697	NM_001292034.3(TAB2):c.102+10del	TAB2	Deletion (intron variant)	not provided	GLikely benign
Select item 1604811	NM_001292034.3(TAB2):c.102+12A>G	TAB2	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2021319	NM_001292034.3(TAB2):c.102+14G>A	TAB2	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1925940	NM_001292034.3(TAB2):c.102+17T>C	TAB2	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1668967	NM_001292034.3(TAB2):c.102+17T>G	TAB2	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2970595	NM_001292034.3(TAB2):c.103-12T>C	TAB2	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2956478	NM_001292034.3(TAB2):c.138C>T (p.Leu46=)	TAB2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1917778	NM_001292034.3(TAB2):c.145G>A (p.Glu49Lys)	TAB2 (E17K +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 729745	NM_001292034.3(TAB2):c.156A>G (p.Arg52=)	TAB2	Single nucleotide variant (synonymous variant)	not provided	GConflicting classifications of pathogenicity
Select item 1594687	NM_001292034.3(TAB2):c.165T>C (p.Tyr55=)	TAB2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2891002	NM_001292034.3(TAB2):c.166G>A (p.Gly56Ser)	TAB2 (G56S +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1803739	NM_001292034.3(TAB2):c.203T>C (p.Ile68Thr)	TAB2 (I36T +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 3006848	NM_001292034.3(TAB2):c.207T>C (p.Ser69=)	TAB2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1473981	NM_001292034.3(TAB2):c.259A>C (p.Ile87Leu)	TAB2 (I87L +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1400161	NM_001292034.3(TAB2):c.277G>A (p.Glu93Lys)	TAB2 (E61K +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GUncertain significance
Select item 1174368	NM_001292034.3(TAB2):c.282A>G (p.Gly94=)	TAB2	Single nucleotide variant (synonymous variant)	not provided	GBenign/Likely benign
Select item 1030405	NM_001292034.3(TAB2):c.287G>A (p.Arg96Lys)	TAB2 (R64K +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 1309279	NM_001292034.3(TAB2):c.311C>T (p.Thr104Met)	TAB2 (T104M +1 more)	Single nucleotide variant (missense variant)	not provided	GConflicting classifications of pathogenicity
Select item 798677	NM_001292034.3(TAB2):c.324T>C (p.Ser108=)	TAB2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1354201	NM_001292034.3(TAB2):c.332A>G (p.Gln111Arg)	TAB2 (Q79R +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2886521	NM_001292034.3(TAB2):c.333A>G (p.Gln111=)	TAB2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1367314	NM_001292034.3(TAB2):c.333A>C (p.Gln111His)	TAB2 (Q79H +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2176639	NM_001292034.3(TAB2):c.344G>T (p.Gly115Val)	TAB2 (G115V +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1533432	NM_001292034.3(TAB2):c.351C>T (p.Ser117=)	TAB2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1368867	NM_001292034.3(TAB2):c.352A>T (p.Asn118Tyr)	TAB2 (N118Y +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GUncertain significance
Select item 2823906	NM_001292034.3(TAB2):c.355A>T (p.Ser119Cys)	TAB2 (S119C +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2749532	NM_001292034.3(TAB2):c.355A>G (p.Ser119Gly)	TAB2 (S119G +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1554981	NM_001292034.3(TAB2):c.375G>A (p.Glu125=)	TAB2	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 1414562	NM_001292034.3(TAB2):c.388C>G (p.Pro130Ala)	TAB2 (P130A +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1949294	NM_001292034.3(TAB2):c.401C>T (p.Pro134Leu)	TAB2 (P102L +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1588254	NM_001292034.3(TAB2):c.438T>C (p.Ser146=)	TAB2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2979772	NM_001292034.3(TAB2):c.462T>G (p.His154Gln)	TAB2 (H122Q +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GUncertain significance
Select item 1551556	NM_001292034.3(TAB2):c.472C>T (p.His158Tyr)	TAB2 (H126Y +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GConflicting classifications of pathogenicity
Select item 1469137	NM_001292034.3(TAB2):c.473A>G (p.His158Arg)	TAB2 (H126R +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2957187	NM_001292034.3(TAB2):c.474C>T (p.His158=)	TAB2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2862721	NM_001292034.3(TAB2):c.500T>A (p.Leu167His)	TAB2 (L135H +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1666818	NM_001292034.3(TAB2):c.507A>G (p.Gln169=)	TAB2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1396868	NM_001292034.3(TAB2):c.509A>G (p.Gln170Arg)	TAB2 (Q170R +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1956884	NM_001292034.3(TAB2):c.518G>A (p.Arg173Lys)	TAB2 (R141K +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2882350	NM_001292034.3(TAB2):c.565C>T (p.Arg189Cys)	TAB2 (R189C +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1428421	NM_001292034.3(TAB2):c.566G>A (p.Arg189His)	TAB2 (R157H +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GUncertain significance
Select item 2983470	NM_001292034.3(TAB2):c.577A>G (p.Thr193Ala)	TAB2 (T161A +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1300827	NM_001292034.3(TAB2):c.597T>G (p.Gly199=)	TAB2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1420715	NM_001292034.3(TAB2):c.617A>G (p.Asn206Ser)	TAB2 (N174S +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2550589	NM_001292034.3(TAB2):c.625C>A (p.Gln209Lys)	TAB2 (Q177K +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 1905430	NM_001292034.3(TAB2):c.641A>G (p.Tyr214Cys)	TAB2 (Y214C +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1973512	NM_001292034.3(TAB2):c.655A>G (p.Ile219Val)	TAB2 (I187V +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1454074	NM_001292034.3(TAB2):c.668del (p.Gly223fs)	LOC126859827, TAB2 (G223fs +1 more)	Deletion (frameshift variant)	not provided	GPathogenic
Select item 2991910	NM_001292034.3(TAB2):c.690A>G (p.Gln230=)	LOC126859827, TAB2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2088989	NM_001292034.3(TAB2):c.698_699dup (p.Gly234fs)	LOC126859827, TAB2 (G234fs +1 more)	Duplication (frameshift variant)	not provided	GPathogenic
Select item 3022047	NM_001292034.3(TAB2):c.713A>G (p.Gln238Arg)	LOC126859827, TAB2 (Q238R +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3009495	NM_001292034.3(TAB2):c.722C>A (p.Pro241His)	LOC126859827, TAB2 (P241H +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2176915	NM_001292034.3(TAB2):c.725T>G (p.Met242Arg)	LOC126859827, TAB2 (M242R +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1480751	NM_001292034.3(TAB2):c.730C>T (p.Pro244Ser)	LOC126859827, TAB2 (P244S +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1800997	NM_001292034.3(TAB2):c.766T>C (p.Trp256Arg)	LOC126859827, TAB2 (W224R +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2185138	NM_001292034.3(TAB2):c.771T>C (p.Thr257=)	LOC126859827, TAB2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1553013	NM_001292034.3(TAB2):c.774T>A (p.Thr258=)	LOC126859827, TAB2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2867936	NM_001292034.3(TAB2):c.779C>T (p.Pro260Leu)	LOC126859827, TAB2 (P228L +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GUncertain significance
Select item 2419777	NM_001292034.3(TAB2):c.827A>C (p.Gln276Pro)	LOC126859827, TAB2 (Q244P +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1312212	NM_001292034.3(TAB2):c.844C>T (p.His282Tyr)	LOC126859827, TAB2 (H250Y +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1629515	NM_001292034.3(TAB2):c.846T>C (p.His282=)	LOC126859827, TAB2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1575311	NM_001292034.3(TAB2):c.858A>G (p.Pro286=)	LOC126859827, TAB2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2976664	NM_001292034.3(TAB2):c.871A>G (p.Thr291Ala)	LOC126859827, TAB2 (T291A +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2703535	NM_001292034.3(TAB2):c.872C>G (p.Thr291Ser)	LOC126859827, TAB2 (T291S +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1540729	NM_001292034.3(TAB2):c.874A>G (p.Thr292Ala)	LOC126859827, TAB2 (T260A +1 more)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 1947439	NM_001292034.3(TAB2):c.897T>C (p.His299=)	LOC126859827, TAB2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1473578	NM_001292034.3(TAB2):c.955A>G (p.Thr319Ala)	LOC126859827, TAB2 (T319A +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1932849	NM_001292034.3(TAB2):c.958G>C (p.Gly320Arg)	LOC126859827, TAB2 (G320R +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1490476	NM_001292034.3(TAB2):c.961C>T (p.Pro321Ser)	LOC126859827, TAB2 (P289S +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1188284	NM_001292034.3(TAB2):c.964C>T (p.Arg322Ter)	LOC126859827, TAB2 (R290* +1 more)	Single nucleotide variant (nonsense)	not provided	GPathogenic
Select item 1669380	NM_001292034.3(TAB2):c.1014T>C (p.Ser338=)	LOC126859827, TAB2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1695798	NM_001292034.3(TAB2):c.1025G>A (p.Arg342His)	LOC126859827, TAB2 (R310H +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases +3 more	GUncertain significance
Select item 373443	NM_001292034.3(TAB2):c.1039C>T (p.Arg347Ter)	LOC126859827, TAB2 (R347* +1 more)	Single nucleotide variant (nonsense)	not provided +5 more	GPathogenic/Likely pathogenic
Select item 2993645	NM_001292034.3(TAB2):c.1040G>A (p.Arg347Gln)	LOC126859827, TAB2 (R315Q +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2875759	NM_001292034.3(TAB2):c.1043C>T (p.Thr348Ile)	LOC126859827, TAB2 (T316I +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2175209	NM_001292034.3(TAB2):c.1067A>G (p.Asn356Ser)	LOC126859827, TAB2 (N356S +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2189156	NM_001292034.3(TAB2):c.1068T>C (p.Asn356=)	LOC126859827, TAB2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1399671	NM_001292034.3(TAB2):c.1070G>C (p.Ser357Thr)	LOC126859827, TAB2 (S357T +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1655167	NM_001292034.3(TAB2):c.1077C>T (p.Thr359=)	LOC126859827, TAB2	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 3007363	NM_001292034.3(TAB2):c.1115G>A (p.Ser372Asn)	LOC126859827, TAB2 (S372N +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2814620	NM_001292034.3(TAB2):c.1119C>T (p.Pro373=)	LOC126859827, TAB2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1465717	NM_001292034.3(TAB2):c.1123A>G (p.Asn375Asp)	LOC126859827, TAB2 (N375D +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1950751	NM_001292034.3(TAB2):c.1127C>T (p.Thr376Met)	LOC126859827, TAB2 (T344M +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 780666	NM_001292034.3(TAB2):c.1128G>A (p.Thr376=)	LOC126859827, TAB2	Single nucleotide variant (synonymous variant)	not provided	GBenign/Likely benign
Select item 1461000	NM_001292034.3(TAB2):c.1145G>A (p.Arg382His)	LOC126859827, TAB2 (R382H +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1554535	NM_001292034.3(TAB2):c.1149T>C (p.Ser383=)	LOC126859827, TAB2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2803951	NM_001292034.3(TAB2):c.1165A>C (p.Ile389Leu)	LOC126859827, TAB2 (I389L +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 1916896	NM_001292034.3(TAB2):c.1173G>A (p.Ala391=)	LOC126859827, TAB2	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 1909136	NM_001292034.3(TAB2):c.1204C>T (p.Arg402Trp)	LOC126859827, TAB2 (R370W +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2069698	NM_001292034.3(TAB2):c.1238_1239del (p.Ser413fs)	LOC126859827, TAB2 (S381fs +1 more)	Microsatellite (frameshift variant)	not provided	GPathogenic
Select item 2709995	NM_001292034.3(TAB2):c.1267T>A (p.Ser423Thr)	LOC126859827, TAB2 (S423T +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1188486	NM_001292034.3(TAB2):c.1308T>G (p.His436Gln)	LOC126859827, TAB2 (H404Q +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 1374419	NM_001292034.3(TAB2):c.1327A>G (p.Ile443Val)	LOC126859827, TAB2 (I411V +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2125184	NM_001292034.3(TAB2):c.1338C>T (p.Asn446=)	LOC126859827, TAB2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1443448	NM_001292034.3(TAB2):c.1348T>A (p.Ser450Thr)	LOC126859827, TAB2 (S418T +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GUncertain significance

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