Colon Cancer: Gene >> TAF9

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000217893
Start	69365470:69365470(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.268G>T
AA Mutation	p.Asp90Tyr(p.D90Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000380822
Start	69352209:69352209(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.371T>A
AA Mutation	p.Ile124Asn(p.I124N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000217893
Start	69365504:69365504(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139330602
CDS Mutation	c.234C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000217893
Start	69365561:69365561(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.177C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000217893
Start	69365656:69365656(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.82delA
AA Mutation	p.Ile28LeufsTer9(p.I28Lfs*9)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000380822
Start	69355652:69355653(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.322dupA
AA Mutation	p.Thr108AsnfsTer5(p.T108Nfs*5)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	inframe_insertion
Transcription ID	ENST00000380822
Start	69352207:69352208(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.372_373insCCA
AA Mutation	p.Ile124_Phe125insPro(p.I124_F125insP)
Mutation Classification	In_Frame_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> TAF9

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000217893
Start	69365458:69365458(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.280G>T
AA Mutation	p.Asp94Tyr(p.D94Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000217893
Start	69365463:69365463(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.275delT
AA Mutation	p.Leu92TyrfsTer2(p.L92Yfs*2)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript