Colon Cancer: Gene >> SFTPA1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000398636
Start	79614079:79614079(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.713G>A
AA Mutation	p.Cys238Tyr(p.C238Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000398636
Start	79614015:79614015(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.649G>A
AA Mutation	p.Ala217Thr(p.A217T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000398636
Start	79613844:79613844(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368889920
CDS Mutation	c.478G>A
AA Mutation	p.Gly160Ser(p.G160S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000398636
Start	79613933:79613933(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.567G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> SFTPA1

No Mutation Annotation!