Colon Cancer: Gene >> HOXC9

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000303450
Start	54002477:54002477(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749476187
CDS Mutation	c.586C>T
AA Mutation	p.Arg196Cys(p.R196C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000303450
Start	54002591:54002591(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.700C>T
AA Mutation	p.Arg234Trp(p.R234W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000303450
Start	54002534:54002534(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762217624
CDS Mutation	c.643A>G
AA Mutation	p.Met215Val(p.M215V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000303450
Start	54000459:54000459(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.271C>T
AA Mutation	p.Arg91Cys(p.R91C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> HOXC9

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000303450
Start	54002574:54002574(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.683T>C
AA Mutation	p.Val228Ala(p.V228A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000303450
Start	54000410:54000410(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs34136736
CDS Mutation	c.222C>T
Mutation Classification	Silent
Feature Type	Transcript