Colon Cancer: Gene >> PPARG

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000287820
Start	12434104:12434104(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1477C>T
AA Mutation	p.Leu493Phe(p.L493F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000287820
Start	12379924:12379924(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200800608
CDS Mutation	c.303G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000287820
Start	12351667:12351667(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.75A>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000287820
Start	12416771:12416771(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.892delC
AA Mutation	p.Leu298CysfsTer38(p.L298Cfs*38)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000287820
Start	12392683:12392683(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.556delA
AA Mutation	p.Ser186ValfsTer47(p.S186Vfs*47)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> PPARG

No Mutation Annotation!