Colon Cancer: Gene >> RAB27B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000262094
Start	54877703:54877703(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.118A>C
AA Mutation	p.Thr40Pro(p.T40P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000262094
Start	54884430:54884430(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.337T>G
AA Mutation	p.Trp113Gly(p.W113G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000262094
Start	54889249:54889249(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.493G>A
AA Mutation	p.Ala165Thr(p.A165T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000262094
Start	54879383:54879383(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.168A>C
AA Mutation	p.Gln56His(p.Q56H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000262094
Start	54889307:54889307(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753780291
CDS Mutation	c.551G>A
AA Mutation	p.Arg184Gln(p.R184Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262094
Start	54889317:54889317(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.561G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262094
Start	54889341:54889341(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.585T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	stop_gained
Transcription ID	ENST00000262094
Start	54889315:54889315(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.559C>T
AA Mutation	p.Gln187Ter(p.Q187*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> RAB27B

No Mutation Annotation!