Colon Cancer: Gene >> CTAG2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000247306
Start	154652434:154652434(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.467G>T
AA Mutation	p.Gly156Val(p.G156V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000247306
Start	154653265:154653265(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.251A>G
AA Mutation	p.Asp84Gly(p.D84G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000247306
Start	154653317:154653317(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200770651
CDS Mutation	c.199G>A
AA Mutation	p.Gly67Ser(p.G67S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000247306
Start	154653304:154653304(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373719423
CDS Mutation	c.212C>T
AA Mutation	p.Ala71Val(p.A71V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000247306
Start	154652541:154652541(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.360G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000247306
Start	154653318:154653318(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.198C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> CTAG2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000247306
Start	154652489:154652489(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782686361
CDS Mutation	c.412C>T
AA Mutation	p.Arg138Trp(p.R138W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000247306
Start	154653318:154653318(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.198C>T
Mutation Classification	Silent
Feature Type	Transcript