Colon Cancer: Gene >> AQP8

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000219660
Start	25227103:25227103(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780774514
CDS Mutation	c.638G>A
AA Mutation	p.Arg213His(p.R213H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000219660
Start	25217401:25217401(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138117795
CDS Mutation	c.216C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000219660
Start	25221502:25221502(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148689630
CDS Mutation	c.306C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000219660
Start	25224481:25224481(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.507C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000219660
Start	25221554:25221554(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs759782104
CDS Mutation	c.363delG
AA Mutation	p.Met122CysfsTer10(p.M122Cfs*10)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_gained
Transcription ID	ENST00000219660
Start	25224388:25224388(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.414G>A
AA Mutation	p.Trp138Ter(p.W138*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> AQP8

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000219660
Start	25221478:25221478(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754887750
CDS Mutation	c.282G>A
Mutation Classification	Silent
Feature Type	Transcript