TACC2[gene] - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 59707	GRCh38/hg38 10q24.31-26.3(chr10:100194215-132432797)x3	EDRF1-AS1, EDRF1-DT +1036 more	Copy number gain	See cases	GPathogenic
Select item 148679	GRCh38/hg38 10q24.31-26.3(chr10:100600492-133622588)x3	GSTO1, GSTO2 +1097 more	Copy number gain	See cases	GPathogenic
Select item 144206	GRCh38/hg38 10q25.1-26.3(chr10:108102587-133620674)x3	LOC126861107, LOC128598885 +802 more	Copy number gain	See cases	GPathogenic
Select item 57507	GRCh38/hg38 10q25.2-26.3(chr10:111313099-133620674)x3	ABLIM1, ABRAXAS2 +679 more	Copy number gain	See cases	GPathogenic
Select item 59728	GRCh38/hg38 10q26.11-26.3(chr10:117866565-133554210)x3	ABRAXAS2, ACADSB +514 more	Copy number gain	See cases	GPathogenic
Select item 57088	GRCh38/hg38 10q26.11-26.13(chr10:119273012-123117390)x3	FGFR2, GRK5 +119 more	Copy number gain	See cases	GPathogenic
Select item 153718	GRCh38/hg38 10q26.11-26.3(chr10:119707856-133613639)x3	LOC130004884, LOC130004885 +438 more	Copy number gain	See cases	GPathogenic
Select item 57403	GRCh38/hg38 10q26.12-26.3(chr10:120454430-133620674)x1	LOC130004881, LOC130004882 +418 more	Copy number loss	See cases	GPathogenic
Select item 150499	GRCh38/hg38 10q26.12-26.3(chr10:120970558-133622588)x1	LOC130005014, LOC130005015 +409 more	Copy number loss	See cases	GPathogenic
Select item 154374	GRCh38/hg38 10q26.13-26.3(chr10:121588992-133620674)x1	FUOM, GLRX3 +399 more	Copy number loss	See cases	GPathogenic
Select item 154670	GRCh38/hg38 10q26.13-26.3(chr10:121918547-133620674)x1	LOC130004911, LOC130004912 +395 more	Copy number loss	See cases	GPathogenic
Select item 2511117	NM_206862.4(TACC2):c.53C>T (p.Thr18Ile)	TACC2 (T18I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3324168	NM_206862.4(TACC2):c.77G>A (p.Gly26Glu)	TACC2 (G26E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3173313	NM_206862.4(TACC2):c.82A>G (p.Ser28Gly)	TACC2 (S28G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3173253	NM_206862.4(TACC2):c.124C>T (p.Pro42Ser)	TACC2 (P42S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2528012	NM_206862.4(TACC2):c.131A>T (p.His44Leu)	TACC2 (H44L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2515244	NM_206862.4(TACC2):c.149T>C (p.Ile50Thr)	TACC2 (I50T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2613112	NM_206862.4(TACC2):c.182C>T (p.Ala61Val)	TACC2 (A61V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2546192	NM_206862.4(TACC2):c.223C>G (p.Pro75Ala)	TACC2 (P75A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3173262	NM_206862.4(TACC2):c.266G>A (p.Gly89Glu)	TACC2 (G89E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2316503	NM_206862.4(TACC2):c.325T>A (p.Ser109Thr)	TACC2 (S109T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2299345	NM_206862.4(TACC2):c.326C>T (p.Ser109Phe)	TACC2 (S109F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3173271	NM_206862.4(TACC2):c.337T>A (p.Phe113Ile)	TACC2 (F113I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2378721	NM_206862.4(TACC2):c.349C>G (p.Pro117Ala)	TACC2 (P117A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2544939	NM_206862.4(TACC2):c.353C>T (p.Pro118Leu)	TACC2 (P118L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2492339	NM_206862.4(TACC2):c.361T>G (p.Cys121Gly)	TACC2 (C121G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3173275	NM_206862.4(TACC2):c.410C>G (p.Ser137Cys)	TACC2 (S137C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3173278	NM_206862.4(TACC2):c.424C>G (p.Pro142Ala)	TACC2 (P142A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 784170	NM_206862.4(TACC2):c.452C>T (p.Ala151Val)	TACC2 (A151V)	Single nucleotide variant (missense variant +1 more)	not provided	GBenign
Select item 3173306	NM_206862.4(TACC2):c.703C>A (p.Pro235Thr)	TACC2 (P235T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 718876	NM_206862.4(TACC2):c.740A>C (p.Gln247Pro)	TACC2 (Q247P)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign
Select item 3324169	NM_206862.4(TACC2):c.838G>T (p.Asp280Tyr)	TACC2 (D280Y)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 709834	NM_206862.4(TACC2):c.887C>T (p.Pro296Leu)	TACC2 (P296L)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign
Select item 3324159	NM_206862.4(TACC2):c.1025C>T (p.Pro342Leu)	TACC2 (P342L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3173251	NM_206862.4(TACC2):c.1114G>A (p.Val372Ile)	TACC2 (V372I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2482227	NM_206862.4(TACC2):c.1171G>C (p.Val391Leu)	TACC2 (V391L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3173252	NM_206862.4(TACC2):c.1196G>C (p.Gly399Ala)	TACC2 (G399A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2379456	NM_206862.4(TACC2):c.1219C>A (p.Pro407Thr)	TACC2 (P407T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2640895	NM_206862.4(TACC2):c.1242G>C (p.Glu414Asp)	TACC2 (E414D)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign
Select item 2281279	NM_206862.4(TACC2):c.1250A>G (p.His417Arg)	TACC2 (H417R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2357387	NM_206862.4(TACC2):c.1382T>C (p.Val461Ala)	TACC2 (V461A)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2360795	NM_206862.4(TACC2):c.1396G>C (p.Val466Leu)	TACC2 (V466L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2623555	NM_206862.4(TACC2):c.1414G>T (p.Val472Leu)	TACC2 (V472L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3173255	NM_206862.4(TACC2):c.1427G>A (p.Gly476Glu)	TACC2 (G476E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2347798	NM_206862.4(TACC2):c.1508C>T (p.Thr503Met)	TACC2 (T503M)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 3324162	NM_206862.4(TACC2):c.1544C>T (p.Pro515Leu)	TACC2 (P515L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2393951	NM_206862.4(TACC2):c.1607C>T (p.Pro536Leu)	TACC2 (P536L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2219325	NM_206862.4(TACC2):c.1619G>A (p.Ser540Asn)	TACC2 (S540N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2526698	NM_206862.4(TACC2):c.1648A>G (p.Thr550Ala)	TACC2 (T550A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2237525	NM_206862.4(TACC2):c.1649C>T (p.Thr550Met)	TACC2 (T550M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2640896	NM_206862.4(TACC2):c.1650G>A (p.Thr550=)	TACC2	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2551460	NM_206862.4(TACC2):c.1727C>G (p.Pro576Arg)	TACC2 (P576R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 744411	NM_206862.4(TACC2):c.1760A>G (p.Asp587Gly)	TACC2 (D587G)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign
Select item 2375350	NM_206862.4(TACC2):c.1763G>T (p.Gly588Val)	TACC2 (G588V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2528746	NM_206862.4(TACC2):c.1771C>T (p.Pro591Ser)	TACC2 (P591S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2327809	NM_206862.4(TACC2):c.1787G>A (p.Gly596Glu)	TACC2 (G596E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2477248	NM_206862.4(TACC2):c.1817G>A (p.Arg606His)	TACC2 (R606H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3173256	NM_206862.4(TACC2):c.1853C>T (p.Pro618Leu)	TACC2 (P618L)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 709835	NM_206862.4(TACC2):c.1859G>A (p.Ser620Asn)	TACC2 (S620N)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign
Select item 3173257	NM_206862.4(TACC2):c.1907C>T (p.Pro636Leu)	TACC2 (P636L)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 3324167	NM_206862.4(TACC2):c.1909A>G (p.Arg637Gly)	TACC2 (R637G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2316011	NM_206862.4(TACC2):c.2005G>T (p.Val669Phe)	TACC2 (V669F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2361773	NM_206862.4(TACC2):c.2021C>G (p.Pro674Arg)	TACC2 (P674R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3173258	NM_206862.4(TACC2):c.2050G>A (p.Glu684Lys)	TACC2 (E684K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3173259	NM_206862.4(TACC2):c.2061C>G (p.Ile687Met)	TACC2 (I687M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2243627	NM_206862.4(TACC2):c.2065G>A (p.Glu689Lys)	TACC2 (E689K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2509926	NM_206862.4(TACC2):c.2115A>C (p.Glu705Asp)	TACC2 (E705D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3324160	NM_206862.4(TACC2):c.2174C>A (p.Pro725Gln)	TACC2 (P725Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2399386	NM_206862.4(TACC2):c.2257G>A (p.Glu753Lys)	TACC2 (E753K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2481397	NM_206862.4(TACC2):c.2284C>A (p.Pro762Thr)	TACC2 (P762T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3324173	NM_206862.4(TACC2):c.2306C>A (p.Ala769Glu)	TACC2 (A769E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2241894	NM_206862.4(TACC2):c.2347C>G (p.Gln783Glu)	TACC2 (Q783E)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 3173260	NM_206862.4(TACC2):c.2381C>T (p.Thr794Met)	TACC2 (T794M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2345016	NM_206862.4(TACC2):c.2383G>A (p.Ala795Thr)	TACC2 (A795T)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 3173261	NM_206862.4(TACC2):c.2485C>G (p.His829Asp)	TACC2 (H829D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2380942	NM_206862.4(TACC2):c.2513A>C (p.Glu838Ala)	TACC2 (E838A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2219275	NM_206862.4(TACC2):c.2530G>A (p.Val844Met)	TACC2 (V844M)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2221424	NM_206862.4(TACC2):c.2555C>T (p.Pro852Leu)	TACC2 (P852L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2279462	NM_206862.4(TACC2):c.2615C>G (p.Ser872Cys)	TACC2 (S872C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2312862	NM_206862.4(TACC2):c.2635G>A (p.Val879Met)	TACC2 (V879M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2225602	NM_206862.4(TACC2):c.2674G>A (p.Gly892Arg)	TACC2 (G892R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3173264	NM_206862.4(TACC2):c.2695T>A (p.Ser899Thr)	TACC2 (S899T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2471320	NM_206862.4(TACC2):c.2720A>G (p.Lys907Arg)	TACC2 (K907R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3173265	NM_206862.4(TACC2):c.2810C>T (p.Thr937Met)	TACC2 (T937M)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2352774	NM_206862.4(TACC2):c.2842C>T (p.Arg948Trp)	TACC2 (R948W)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2279228	NM_206862.4(TACC2):c.2975A>C (p.Lys992Thr)	TACC2 (K992T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3173266	NM_206862.4(TACC2):c.2987C>A (p.Ala996Glu)	TACC2 (A996E)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 3173267	NM_206862.4(TACC2):c.3020A>G (p.His1007Arg)	TACC2 (H1007R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3173268	NM_206862.4(TACC2):c.3076C>T (p.Pro1026Ser)	TACC2 (P1026S)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 786417	NM_206862.4(TACC2):c.3100G>A (p.Glu1034Lys)	TACC2 (E1034K)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign
Select item 3173269	NM_206862.4(TACC2):c.3127G>A (p.Ala1043Thr)	TACC2 (A1043T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3025023	NM_206862.4(TACC2):c.3134C>T (p.Pro1045Leu)	TACC2 (P1045L)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign
Select item 3173270	NM_206862.4(TACC2):c.3281C>T (p.Pro1094Leu)	TACC2 (P1094L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 1686344	NM_206862.4(TACC2):c.3317C>G (p.Ser1106Trp)	TACC2 (S1106W)	Single nucleotide variant (missense variant +1 more)	not specified	GBenign
Select item 3324164	NM_206862.4(TACC2):c.3352C>G (p.Pro1118Ala)	TACC2 (P1118A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2322666	NM_206862.4(TACC2):c.3368A>G (p.Gln1123Arg)	TACC2 (Q1123R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2311086	NM_206862.4(TACC2):c.3373G>A (p.Gly1125Ser)	TACC2 (G1125S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2281697	NM_206862.4(TACC2):c.3391G>A (p.Glu1131Lys)	TACC2 (E1131K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2207487	NM_206862.4(TACC2):c.3460A>G (p.Thr1154Ala)	TACC2 (T1154A)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2640897	NM_206862.4(TACC2):c.3504C>T (p.Ser1168=)	TACC2	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign

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