Colon Cancer: Gene >> HPCA

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000373467
Start	32888924:32888924(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774794783
CDS Mutation	c.26G>A
AA Mutation	p.Arg9Gln(p.R9Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000373467
Start	32889271:32889271(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138767632
CDS Mutation	c.373G>A
AA Mutation	p.Val125Met(p.V125M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000373467
Start	32889250:32889250(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.352C>T
AA Mutation	p.Arg118Trp(p.R118W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000373467
Start	32888964:32888964(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.66C>A
AA Mutation	p.Phe22Leu(p.F22L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373467
Start	32889054:32889054(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758411778
CDS Mutation	c.156C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> HPCA

No Mutation Annotation!