Colon Cancer: Gene >> INSIG1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000340368
Start	155302788:155302788(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.746C>T
AA Mutation	p.Pro249Leu(p.P249L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000340368
Start	155302810:155302810(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs576061560
CDS Mutation	c.768C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000340368
Start	155302379:155302379(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs562345271
CDS Mutation	c.666G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	stop_gained
Transcription ID	ENST00000340368
Start	155302832:155302832(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.790C>T
AA Mutation	p.Arg264Ter(p.R264*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000340368
Start	155298561:155298563(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.276_278delCTC
AA Mutation	p.Phe92_Ser93delinsLeu(p.F92_S93delinsL)
Mutation Classification	In_Frame_Del
Feature Type	Transcript

Rectum Cancer: Gene >> INSIG1

No Mutation Annotation!