Colon Cancer: Gene >> GTF2I

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000573035
Start	74689214:74689214(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.86C>A
AA Mutation	p.Ala29Asp(p.A29D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000573035
Start	74716950:74716950(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.880G>A
AA Mutation	p.Asp294Asn(p.D294N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000573035
Start	74689226:74689226(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.98T>C
AA Mutation	p.Met33Thr(p.M33T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000573035
Start	74691096:74691096(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.223G>T
AA Mutation	p.Asp75Tyr(p.D75Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000573035
Start	74700359:74700359(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148927442
CDS Mutation	c.486C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000573035
Start	74733926:74733926(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782143965
CDS Mutation	c.1308T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000573035
Start	74700609:74700609(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.566delT
AA Mutation	p.Leu189Ter(p.L189*)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	stop_gained;frameshift_variant
Transcription ID	ENST00000573035
Start	74732598:74732599(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1241dupA
AA Mutation	p.Tyr414Ter(p.Y414*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> GTF2I

No Mutation Annotation!