Colon Cancer: Gene >> PRMT5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000324366
Start	22923140:22923140(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1396G>A
AA Mutation	p.Gly466Arg(p.G466R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000324366
Start	22924962:22924962(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.856T>C
AA Mutation	p.Tyr286His(p.Y286H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000324366
Start	22922539:22922539(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1600C>T
AA Mutation	p.Arg534Cys(p.R534C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000324366
Start	22928150:22928150(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.291G>C
AA Mutation	p.Glu97Asp(p.E97D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000324366
Start	22924921:22924921(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.897C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000324366
Start	22922242:22922242(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1697-2A>C
Mutation Classification	Splice_Site
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	start_lost
Transcription ID	ENST00000324366
Start	22929361:22929361(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1A>G
AA Mutation	p.Met1?(p.M1?)
Mutation Classification	Translation_Start_Site
Feature Type	Transcript

Rectum Cancer: Gene >> PRMT5

No Mutation Annotation!