Colon Cancer: Gene >> TACC3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000313288
Start	1728781:1728781(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1379T>G
AA Mutation	p.Leu460Arg(p.L460R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000313288
Start	1728129:1728129(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.727G>A
AA Mutation	p.Ala243Thr(p.A243T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000313288
Start	1740981:1740981(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2218C>T
AA Mutation	p.Arg740Cys(p.R740C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000313288
Start	1723530:1723530(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373800152
CDS Mutation	c.109C>T
AA Mutation	p.Arg37Cys(p.R37C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000313288
Start	1728657:1728657(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1255G>A
AA Mutation	p.Gly419Arg(p.G419R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000313288
Start	1737297:1737297(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1805A>G
AA Mutation	p.Glu602Gly(p.E602G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000313288
Start	1723434:1723434(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.13G>T
AA Mutation	p.Val5Phe(p.V5F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000313288
Start	1723783:1723783(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.218G>T
AA Mutation	p.Ser73Ile(p.S73I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000313288
Start	1739757:1739757(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1997A>G
AA Mutation	p.His666Arg(p.H666R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000313288
Start	1728492:1728492(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1090A>G
AA Mutation	p.Lys364Glu(p.K364E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000313288
Start	1728536:1728536(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772058052
CDS Mutation	c.1134G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000313288
Start	1744808:1744808(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372855233
CDS Mutation	c.2427G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000313288
Start	1735289:1735289(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs202067228
CDS Mutation	c.1608G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000313288
Start	1728656:1728656(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1254C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000313288
Start	1723788:1723789(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.223_224insT
AA Mutation	p.Ala75ValfsTer5(p.A75Vfs*5)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	splice_acceptor_variant;coding_sequence_variant;intron_variant
Transcription ID	ENST00000313288
Start	1744694:1744760(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2331-18_2379delCCGCCCCTACCCCTCCAGGGCAAACGAGGAGATCGCCCAGGTCCGGAGCAAGGCCCAGGCGGAAGCG
Mutation Classification	Splice_Site
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000313288
Start	1735271:1735271(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1592-2A>G
Mutation Classification	Splice_Site
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	inframe_insertion
Transcription ID	ENST00000313288
Start	1731227:1731228(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.1521_1526dupAGTGCC
AA Mutation	p.Val508_Pro509dup(p.V508_P509dup)
Mutation Classification	In_Frame_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> TACC3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000313288
Start	1728598:1728598(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1196C>A
AA Mutation	p.Ser399Tyr(p.S399Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript