Colon Cancer: Gene >> SUGT1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000343788
Start	52653052:52653052(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764131039
CDS Mutation	c.45C>A
AA Mutation	p.Phe15Leu(p.F15L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000343788
Start	52687741:52687741(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1004C>T
AA Mutation	p.Ser335Leu(p.S335L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000343788
Start	52658433:52658433(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.222C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000343788
Start	52663106:52663106(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.489T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000343788
Start	52680152:52680152(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.993C>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> SUGT1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000343788
Start	52687755:52687755(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1018T>G
AA Mutation	p.Leu340Val(p.L340V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000343788
Start	52676301:52676301(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs535411991
CDS Mutation	c.795G>A
Mutation Classification	Silent
Feature Type	Transcript