Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> GCNT3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000396065
Start	59619179:59619179(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.941A>C
AA Mutation	p.Lys314Thr(p.K314T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000396065
Start	59618890:59618890(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.652G>C
AA Mutation	p.Val218Leu(p.V218L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000396065
Start	59618259:59618259(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767379702
CDS Mutation	c.21C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	stop_gained
Transcription ID	ENST00000396065
Start	59619196:59619196(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.958G>T
AA Mutation	p.Glu320Ter(p.E320*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> GCNT3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000396065
Start	59618355:59618355(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.117C>A
AA Mutation	p.His39Gln(p.H39Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000396065
Start	59619171:59619171(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.933G>T
AA Mutation	p.Lys311Asn(p.K311N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	stop_gained
Transcription ID	ENST00000396065
Start	59618746:59618746(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.508G>T
AA Mutation	p.Glu170Ter(p.E170*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript