Colon Cancer: Gene >> CENPW

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000368328
Start	126346236:126346236(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745347945
CDS Mutation	c.158G>A
AA Mutation	p.Arg53Gln(p.R53Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000368328
Start	126348482:126348482(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.257G>T
AA Mutation	p.Ser86Ile(p.S86I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	start_lost
Transcription ID	ENST00000368328
Start	126340276:126340276(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3G>A
AA Mutation	p.Met1?(p.M1?)
Mutation Classification	Translation_Start_Site
Feature Type	Transcript

Rectum Cancer: Gene >> CENPW

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000368328
Start	126346206:126346206(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.128T>A
AA Mutation	p.Val43Asp(p.V43D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000368328
Start	126346270:126346270(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773583292
CDS Mutation	c.192G>A
Mutation Classification	Silent
Feature Type	Transcript