Colon Cancer: Gene >> THRA

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000264637
Start	40088372:40088372(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.854A>G
AA Mutation	p.Glu285Gly(p.E285G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000264637
Start	40088389:40088389(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.871G>A
AA Mutation	p.Gly291Ser(p.G291S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000264637
Start	40086839:40086839(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.709C>T
AA Mutation	p.Pro237Ser(p.P237S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000264637
Start	40084712:40084712(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.473C>A
AA Mutation	p.Pro158Gln(p.P158Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264637
Start	40088409:40088409(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.891C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> THRA

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000264637
Start	40084672:40084672(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.433C>T
AA Mutation	p.Arg145Trp(p.R145W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript