Colon Cancer: Gene >> CTSS

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000368985
Start	150751917:150751917(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.491C>T
AA Mutation	p.Ala164Val(p.A164V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000368985
Start	150755075:150755075(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.325T>G
AA Mutation	p.Ser109Ala(p.S109A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000368985
Start	150764648:150764648(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.116A>G
AA Mutation	p.Tyr39Cys(p.Y39C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000368985
Start	150750034:150750034(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.765T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000368985
Start	150757946:150757946(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.161delA
AA Mutation	p.Lys54ArgfsTer3(p.K54Rfs*3)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> CTSS

No Mutation Annotation!