Colon Cancer: Gene >> GPR68

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000531499
Start	91234860:91234860(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.191C>T
AA Mutation	p.Thr64Met(p.T64M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000531499
Start	91234894:91234894(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.157C>T
AA Mutation	p.Arg53Trp(p.R53W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000531499
Start	91234387:91234387(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.664C>T
AA Mutation	p.Arg222Cys(p.R222C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000531499
Start	91234504:91234504(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149975079
CDS Mutation	c.547C>T
AA Mutation	p.Arg183Cys(p.R183C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000531499
Start	91234155:91234155(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.896G>A
AA Mutation	p.Arg299His(p.R299H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000531499
Start	91234012:91234012(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1039G>A
AA Mutation	p.Ala347Thr(p.A347T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000531499
Start	91234309:91234309(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.742C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000531499
Start	91234262:91234262(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.789C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> GPR68

No Mutation Annotation!