Colon Cancer: Gene >> PLSCR2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000497985
Start	146449298:146449298(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.772G>A
AA Mutation	p.Ala258Thr(p.A258T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000497985
Start	146458441:146458441(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.289C>A
AA Mutation	p.Leu97Ile(p.L97I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000497985
Start	146449316:146449316(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.754T>C
AA Mutation	p.Ser252Pro(p.S252P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000497985
Start	146459960:146459960(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.164G>T
AA Mutation	p.Gly55Val(p.G55V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000497985
Start	146455363:146455363(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140953829
CDS Mutation	c.416G>A
AA Mutation	p.Arg139Gln(p.R139Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_gained
Transcription ID	ENST00000497985
Start	146449301:146449301(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.769G>T
AA Mutation	p.Glu257Ter(p.E257*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> PLSCR2

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000497985
Start	146459856:146459856(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.268T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	stop_gained
Transcription ID	ENST00000497985
Start	146449301:146449301(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.769G>T
AA Mutation	p.Glu257Ter(p.E257*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript