Colon Cancer: Gene >> EBAG9

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000337573
Start	109564476:109564476(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200319904
CDS Mutation	c.559G>A
AA Mutation	p.Glu187Lys(p.E187K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000337573
Start	109550843:109550843(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751442457
CDS Mutation	c.19C>T
AA Mutation	p.Arg7Trp(p.R7W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000337573
Start	109554860:109554860(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.294G>T
AA Mutation	p.Met98Ile(p.M98I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000337573
Start	109564535:109564535(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.618C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000337573
Start	109560906:109560906(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.498C>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> EBAG9

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000337573
Start	109554869:109554869(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.303T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000337573
Start	109554785:109554785(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.219C>T
Mutation Classification	Silent
Feature Type	Transcript