Colon Cancer: Gene >> FGL2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000248598
Start	77196496:77196496(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1103C>A
AA Mutation	p.Ser368Tyr(p.S368Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000248598
Start	77199395:77199395(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767168412
CDS Mutation	c.399A>C
AA Mutation	p.Leu133Phe(p.L133F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000248598
Start	77196669:77196669(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs3093278
CDS Mutation	c.930C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000248598
Start	77196465:77196465(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1134C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000248598
Start	77196327:77196327(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1272C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_gained
Transcription ID	ENST00000248598
Start	77196794:77196794(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.805C>T
AA Mutation	p.Gln269Ter(p.Q269*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> FGL2

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000248598
Start	77196948:77196948(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs566096585
CDS Mutation	c.651C>T
Mutation Classification	Silent
Feature Type	Transcript