Colon Cancer: Gene >> GSS

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000216951
Start	34928925:34928925(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1328A>C
AA Mutation	p.Lys443Thr(p.K443T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000216951
Start	34936775:34936775(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780544238
CDS Mutation	c.755G>A
AA Mutation	p.Arg252Gln(p.R252Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000216951
Start	34932028:34932028(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.940C>T
AA Mutation	p.Pro314Ser(p.P314S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000216951
Start	34951835:34951835(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.18delG
AA Mutation	p.Ser7AlafsTer9(p.S7Afs*9)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> GSS

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000216951
Start	34941780:34941780(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.541T>C
AA Mutation	p.Ser181Pro(p.S181P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000216951
Start	34941724:34941724(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749301244
CDS Mutation	c.597C>T
Mutation Classification	Silent
Feature Type	Transcript