Colon Cancer: Gene >> WLS

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000262348
Start	68150289:68150289(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.871T>G
AA Mutation	p.Phe291Val(p.F291V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000262348
Start	68194176:68194176(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.158C>T
AA Mutation	p.Ala53Val(p.A53V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000262348
Start	68159172:68159172(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.455C>T
AA Mutation	p.Ala152Val(p.A152V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000262348
Start	68150234:68150234(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764615459
CDS Mutation	c.926C>T
AA Mutation	p.Ala309Val(p.A309V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000354777
Start	68098650:68098650(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs561611966
CDS Mutation	c.1614C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262348
Start	68159153:68159153(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.474G>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> WLS

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000262348
Start	68153634:68153634(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.686G>T
AA Mutation	p.Gly229Val(p.G229V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000354777
Start	68098732:68098732(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776089916
CDS Mutation	c.1532C>T
AA Mutation	p.Ser511Leu(p.S511L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript