Mutation

Primary Site >> Liver Cancer

Gene >> TACC2

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000334433
Start	122086483:122086483(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3983G>T
AA Mutation	p.Cys1328Phe(p.C1328F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000334433
Start	122210889:122210889(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.6464A>T
AA Mutation	p.Gln2155Leu(p.Q2155L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000334433
Start	122084671:122084671(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2171C>T
AA Mutation	p.Pro724Leu(p.P724L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000334433
Start	122085212:122085212(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2712G>T
AA Mutation	p.Gln904His(p.Q904H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000334433
Start	122211293:122211293(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.6868G>T
AA Mutation	p.Gly2290Cys(p.G2290C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000334433
Start	122084436:122084436(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1936G>T
AA Mutation	p.Gly646Trp(p.G646W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000334433
Start	122084770:122084770(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201466757
CDS Mutation	c.2270C>T
AA Mutation	p.Thr757Met(p.T757M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000334433
Start	122087021:122087021(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4521G>T
Mutation Classification	Silent
Feature Type	Transcript

ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000334433
Start	122143611:122143611(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5739G>C
Mutation Classification	Silent
Feature Type	Transcript

ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000334433
Start	122210407:122210407(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5982T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000334433
Start	122083526:122083526(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1026G>T
Mutation Classification	Silent
Feature Type	Transcript