Colon Cancer: Gene >> PAX9

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000361487
Start	36663131:36663131(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.239C>T
AA Mutation	p.Thr80Ile(p.T80I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000361487
Start	36663496:36663496(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.604C>A
AA Mutation	p.Leu202Met(p.L202M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000361487
Start	36663206:36663206(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752908209
CDS Mutation	c.314G>A
AA Mutation	p.Arg105His(p.R105H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000361487
Start	36663215:36663215(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748361932
CDS Mutation	c.323C>T
AA Mutation	p.Ala108Val(p.A108V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361487
Start	36666544:36666544(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.714G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361487
Start	36663342:36663342(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.450G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> PAX9

No Mutation Annotation!