Colon Cancer: Gene >> TINF2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000267415
Start	24242304:24242304(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.29C>T
AA Mutation	p.Ala10Val(p.A10V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000267415
Start	24240660:24240660(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.820T>C
AA Mutation	p.Ser274Pro(p.S274P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000267415
Start	24240689:24240689(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.791G>A
AA Mutation	p.Gly264Asp(p.G264D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000267415
Start	24240715:24240715(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.765C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000267415
Start	24241105:24241105(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.519G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000267415
Start	24241078:24241079(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.545_546delCT
AA Mutation	p.Ser182TyrfsTer25(p.S182Yfs*25)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000267415
Start	24240470:24240470(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1010delG
AA Mutation	p.Gly337GlufsTer4(p.G337Efs*4)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> TINF2

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000267415
Start	24239815:24239815(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1338C>T
Mutation Classification	Silent
Feature Type	Transcript