Mutation

Primary Site >> Stomach Cancer

Gene >> TACC2

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000334433
Start	122210820:122210820(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs202246830
CDS Mutation	c.6395C>T
AA Mutation	p.Pro2132Leu(p.P2132L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000334433
Start	122083821:122083821(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1321T>A
AA Mutation	p.Ser441Thr(p.S441T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000334433
Start	122083429:122083429(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773078761
CDS Mutation	c.929G>A
AA Mutation	p.Cys310Tyr(p.C310Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000334433
Start	122087853:122087853(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5353A>G
AA Mutation	p.Ile1785Val(p.I1785V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000334433
Start	122229388:122229388(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.7939A>G
AA Mutation	p.Ser2647Gly(p.S2647G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000334433
Start	122086245:122086245(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3745G>A
AA Mutation	p.Glu1249Lys(p.E1249K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000334433
Start	122238004:122238004(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.8315A>G
AA Mutation	p.Tyr2772Cys(p.Y2772C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000334433
Start	122050497:122050497(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.93A>G
AA Mutation	p.Ile31Met(p.I31M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000334433
Start	122143600:122143600(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5728C>G
AA Mutation	p.Leu1910Val(p.L1910V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000334433
Start	122132673:122132673(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5638G>A
AA Mutation	p.Ala1880Thr(p.A1880T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000334433
Start	122143633:122143633(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5761C>A
AA Mutation	p.Pro1921Thr(p.P1921T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000334433
Start	122216801:122216801(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.7519G>A
AA Mutation	p.Glu2507Lys(p.E2507K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000334433
Start	122082843:122082843(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373788566
CDS Mutation	c.343G>A
AA Mutation	p.Glu115Lys(p.E115K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000334433
Start	122216809:122216809(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.7527A>C
AA Mutation	p.Lys2509Asn(p.K2509N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000334433
Start	122248802:122248802(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.8552A>G
AA Mutation	p.Lys2851Arg(p.K2851R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000334433
Start	122082744:122082744(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.244A>G
AA Mutation	p.Lys82Glu(p.K82E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000334433
Start	122083966:122083966(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1466T>C
AA Mutation	p.Val489Ala(p.V489A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000334433
Start	122211161:122211161(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.6736A>G
AA Mutation	p.Thr2246Ala(p.T2246A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000334433
Start	122085411:122085411(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2911G>T
AA Mutation	p.Asp971Tyr(p.D971Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000334433
Start	122085319:122085319(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2819A>C
AA Mutation	p.Lys940Thr(p.K940T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	21
Mutation Consequence	missense_variant
Transcription ID	ENST00000334433
Start	122230388:122230388(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.8075T>C
AA Mutation	p.Leu2692Pro(p.L2692P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	22
Mutation Consequence	missense_variant
Transcription ID	ENST00000334433
Start	122086497:122086497(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3997C>T
AA Mutation	p.Pro1333Ser(p.P1333S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000334433
Start	122021990:122021990(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.9T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000334433
Start	122229375:122229375(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.7926T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000334433
Start	122083682:122083682(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368657688
CDS Mutation	c.1182C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000334433
Start	122083781:122083781(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1281T>A
Mutation Classification	Silent
Feature Type	Transcript

ID	27
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000334433
Start	122211697:122211697(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762718237
CDS Mutation	c.7272G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	28
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000334433
Start	122086040:122086040(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3540C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	29
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000334433
Start	122087954:122087954(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5454T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	30
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000334433
Start	122086667:122086667(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4167A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	31
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000334433
Start	122083136:122083136(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.636G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	32
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000334433
Start	122211073:122211073(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149346540
CDS Mutation	c.6648G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	33
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000334433
Start	122254026:122254026(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779260986
CDS Mutation	c.8817C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	34
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000334433
Start	122083223:122083223(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.727delG
AA Mutation	p.Val243TrpfsTer6(p.V243Wfs*6)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	35
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000334433
Start	122084849:122084849(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2353delG
AA Mutation	p.Glu785ArgfsTer30(p.E785Rfs*30)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	36
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000334433
Start	122211067:122211067(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.6647delC
AA Mutation	p.Pro2216ArgfsTer30(p.P2216Rfs*30)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	37
Mutation Consequence	stop_gained
Transcription ID	ENST00000334433
Start	122249569:122249569(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.8686C>T
AA Mutation	p.Arg2896Ter(p.R2896*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	38
Mutation Consequence	stop_gained
Transcription ID	ENST00000334433
Start	122085933:122085933(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3433C>T
AA Mutation	p.Gln1145Ter(p.Q1145*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	39
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000334433
Start	122143708:122143708(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5834+2T>C
Mutation Classification	Splice_Site
Feature Type	Transcript