Colon Cancer: Gene >> GNG4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000366597
Start	235552140:235552140(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756924811
CDS Mutation	c.197G>A
AA Mutation	p.Arg66His(p.R66H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000366597
Start	235552189:235552189(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.148C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	start_lost
Transcription ID	ENST00000366597
Start	235583836:235583836(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3G>A
AA Mutation	p.Met1?(p.M1?)
Mutation Classification	Translation_Start_Site
Feature Type	Transcript

Rectum Cancer: Gene >> GNG4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000366597
Start	235552141:235552141(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764998095
CDS Mutation	c.196C>T
AA Mutation	p.Arg66Cys(p.R66C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000366597
Start	235552139:235552139(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.198C>T
Mutation Classification	Silent
Feature Type	Transcript