Colon Cancer: Gene >> STRAP

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000419869
Start	15883558:15883558(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.130C>T
AA Mutation	p.Arg44Cys(p.R44C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000419869
Start	15882756:15882756(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.49G>A
AA Mutation	p.Val17Met(p.V17M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000419869
Start	15895420:15895420(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.562A>C
AA Mutation	p.Ser188Arg(p.S188R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000419869
Start	15900038:15900038(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.910A>G
AA Mutation	p.Lys304Glu(p.K304E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000419869
Start	15897969:15897969(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.726T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000419869
Start	15883590:15883590(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.162A>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000419869
Start	15894081:15894081(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.444delA
AA Mutation	p.Ala149LeufsTer26(p.A149Lfs*26)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> STRAP

No Mutation Annotation!