Colon Cancer: Gene >> PLSCR1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000342435
Start	146521630:146521630(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.652A>G
AA Mutation	p.Thr218Ala(p.T218A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000342435
Start	146517056:146517056(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.850G>T
AA Mutation	p.Asp284Tyr(p.D284Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000342435
Start	146522017:146522017(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.392T>G
AA Mutation	p.Ile131Ser(p.I131S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000342435
Start	146517145:146517145(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.761G>A
AA Mutation	p.Cys254Tyr(p.C254Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000342435
Start	146521895:146521895(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779164394
CDS Mutation	c.514G>A
AA Mutation	p.Val172Ile(p.V172I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> PLSCR1

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000342435
Start	146521610:146521610(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201312426
CDS Mutation	c.672A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000342435
Start	146528662:146528662(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747622828
CDS Mutation	c.264G>A
Mutation Classification	Silent
Feature Type	Transcript