Colon Cancer: Gene >> ACTL6A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000429709
Start	179576896:179576896(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773240025
CDS Mutation	c.751C>T
AA Mutation	p.His251Tyr(p.H251Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000429709
Start	179576251:179576251(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.511G>A
AA Mutation	p.Asp171Asn(p.D171N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000429709
Start	179586589:179586589(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1166G>A
AA Mutation	p.Arg389Gln(p.R389Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000429709
Start	179574394:179574394(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.403A>C
AA Mutation	p.Lys135Gln(p.K135Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000429709
Start	179586589:179586589(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1166G>T
AA Mutation	p.Arg389Leu(p.R389L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000429709
Start	179574393:179574393(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.402G>T
AA Mutation	p.Glu134Asp(p.E134D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000429709
Start	179573406:179573406(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.315T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000429709
Start	179563113:179563113(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.21G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000429709
Start	179583430:179583430(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1104G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	stop_gained
Transcription ID	ENST00000429709
Start	179576895:179576895(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.750G>A
AA Mutation	p.Trp250Ter(p.W250*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000429709
Start	179570065:179570065(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.103-2A>G
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> ACTL6A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000429709
Start	179586552:179586552(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1129C>T
AA Mutation	p.Arg377Trp(p.R377W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	stop_gained
Transcription ID	ENST00000429709
Start	179587969:179587969(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1249G>T
AA Mutation	p.Glu417Ter(p.E417*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript