Colon Cancer: Gene >> FADS1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000350997
Start	61816730:61816730(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.200C>G
AA Mutation	p.Thr67Ser(p.T67S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000350997
Start	61810808:61810808(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.858C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000350997
Start	61816708:61816708(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.222G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000350997
Start	61816731:61816732(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.198_199insGTGAAGT
AA Mutation	p.Thr67ValfsTer34(p.T67Vfs*34)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> FADS1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000350997
Start	61813251:61813251(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.478A>T
AA Mutation	p.Thr160Ser(p.T160S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript