Colon Cancer: Gene >> SHOX2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000441443
Start	158102724:158102724(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.509G>A
AA Mutation	p.Arg170Gln(p.R170Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000441443
Start	158098315:158098315(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.708T>G
AA Mutation	p.Ser236Arg(p.S236R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000441443
Start	158102753:158102753(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.480C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> SHOX2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000441443
Start	158099925:158099925(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.637C>G
AA Mutation	p.Gln213Glu(p.Q213E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000441443
Start	158102853:158102853(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747319392
CDS Mutation	c.380C>T
AA Mutation	p.Ala127Val(p.A127V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript