Colon Cancer: Gene >> GJB3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000373362
Start	34784850:34784850(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373725070
CDS Mutation	c.88G>A
AA Mutation	p.Val30Ile(p.V30I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000373362
Start	34785240:34785240(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759759043
CDS Mutation	c.478C>T
AA Mutation	p.Arg160Cys(p.R160C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000373362
Start	34784886:34784886(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.124C>T
AA Mutation	p.Arg42Cys(p.R42C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000373362
Start	34785217:34785217(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.455T>A
AA Mutation	p.Leu152His(p.L152H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373362
Start	34785218:34785218(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.456C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373362
Start	34785326:34785326(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.564C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373362
Start	34784822:34784822(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778017222
CDS Mutation	c.60C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000373362
Start	34785265:34785265(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.507delC
AA Mutation	p.Cys170AlafsTer98(p.C170Afs*98)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000373362
Start	34785435:34785435(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.677delG
AA Mutation	p.Gly226ValfsTer42(p.G226Vfs*42)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> GJB3

No Mutation Annotation!