Colon Cancer: Gene >> SKI

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000378536
Start	2229658:2229658(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.892G>A
AA Mutation	p.Ala298Thr(p.A298T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000378536
Start	2229319:2229319(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.553C>A
AA Mutation	p.Leu185Met(p.L185M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000378536
Start	2304028:2304028(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752151031
CDS Mutation	c.1400C>T
AA Mutation	p.Thr467Met(p.T467M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000378536
Start	2304004:2304004(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1376T>C
AA Mutation	p.Val459Ala(p.V459A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000378536
Start	2303882:2303882(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs536126761
CDS Mutation	c.1254C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000378536
Start	2306112:2306112(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1860C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> SKI

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000378536
Start	2304488:2304488(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1670A>T
AA Mutation	p.Glu557Val(p.E557V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript