Colon Cancer: Gene >> CD8B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000390655
Start	86858180:86858180(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747895168
CDS Mutation	c.280C>T
AA Mutation	p.Arg94Trp(p.R94W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000331469
Start	86815640:86815640(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.699G>T
AA Mutation	p.Gln233His(p.Q233H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000390655
Start	86846746:86846746(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.521G>A
AA Mutation	p.Gly174Asp(p.G174D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000331469
Start	86815611:86815611(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.728C>T
AA Mutation	p.Thr243Ile(p.T243I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000390655
Start	86846730:86846730(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368685988
CDS Mutation	c.537C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_gained;inframe_insertion
Transcription ID	ENST00000390655
Start	86853015:86853016(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.474_475insTAGCTT
AA Mutation	p.Pro158_Arg159insTer(p.P158_R159ins*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> CD8B

No Mutation Annotation!