Colon Cancer: Gene >> CAPG

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000263867
Start	85401809:85401809(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.172G>T
AA Mutation	p.Val58Phe(p.V58F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000263867
Start	85395552:85395552(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs566538644
CDS Mutation	c.967G>A
AA Mutation	p.Ala323Thr(p.A323T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000263867
Start	85395617:85395617(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.902C>T
AA Mutation	p.Ala301Val(p.A301V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263867
Start	85395616:85395616(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.903G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263867
Start	85401622:85401622(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs2229669
CDS Mutation	c.258G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263867
Start	85398702:85398702(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.747A>G
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> CAPG

Mutation ID	1
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000263867
Start	85402127:85402127(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.19delC
AA Mutation	p.Gln7ArgfsTer23(p.Q7Rfs*23)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript