Colon Cancer: Gene >> CCNG2

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000316355
Start	77164275:77164275(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.707T>C
AA Mutation	p.Ile236Thr(p.I236T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000316355
Start	77165827:77165827(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.938G>A
AA Mutation	p.Cys313Tyr(p.C313Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000316355
Start	77164342:77164342(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.774T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000316355
Start	77159433:77159433(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.210delT
AA Mutation	p.Phe70LeufsTer22(p.F70Lfs*22)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000316355
Start	77160874:77160875(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.430_431insACAAGAGGCTTCT
AA Mutation	p.Ile144AsnfsTer13(p.I144Nfs*13)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> CCNG2

No Mutation Annotation!