Colon Cancer: Gene >> TUBB

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000327892
Start	30724350:30724350(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772090260
CDS Mutation	c.1288G>A
AA Mutation	p.Ala430Thr(p.A430T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000327892
Start	30724077:30724077(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1015A>G
AA Mutation	p.Ser339Gly(p.S339G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000327892
Start	30724013:30724013(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.951C>A
AA Mutation	p.Phe317Leu(p.F317L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000327892
Start	30723578:30723578(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.516A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000327892
Start	30724370:30724370(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs3873307
CDS Mutation	c.1308C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000327892
Start	30723389:30723389(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139202417
CDS Mutation	c.327C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000327892
Start	30723483:30723483(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.425delG
AA Mutation	p.Gly142AlafsTer23(p.G142Afs*23)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> TUBB

No Mutation Annotation!