Colon Cancer: Gene >> ACTG2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000345517
Start	73919512:73919512(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1068G>A
AA Mutation	p.Met356Ile(p.M356I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000345517
Start	73913565:73913565(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs78001248
CDS Mutation	c.532C>T
AA Mutation	p.Arg178Cys(p.R178C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000345517
Start	73901337:73901337(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.26T>C
AA Mutation	p.Leu9Pro(p.L9P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000345517
Start	73914698:73914698(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.632G>A
AA Mutation	p.Arg211Gln(p.R211Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000345517
Start	73902415:73902415(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.182G>T
AA Mutation	p.Ser61Ile(p.S61I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000345517
Start	73916587:73916587(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.809T>C
AA Mutation	p.Met270Thr(p.M270T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000345517
Start	73916739:73916739(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.961C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000345517
Start	73901390:73901391(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.85dupC
AA Mutation	p.Arg29ProfsTer30(p.R29Pfs*30)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> ACTG2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000345517
Start	73916725:73916725(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.947A>C
AA Mutation	p.Lys316Thr(p.K316T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript