Colon Cancer: Gene >> ACTB

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000331789
Start	5529295:5529295(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.229A>T
AA Mutation	p.Thr77Ser(p.T77S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000331789
Start	5529653:5529653(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5A>C
AA Mutation	p.Asp2Ala(p.D2A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000331789
Start	5528493:5528493(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.590G>A
AA Mutation	p.Gly197Asp(p.G197D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000331789
Start	5528425:5528425(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.658G>A
AA Mutation	p.Ala220Thr(p.A220T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000331789
Start	5527762:5527762(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1114C>T
AA Mutation	p.Arg372Cys(p.R372C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000331789
Start	5529222:5529222(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.302A>G
AA Mutation	p.His101Arg(p.H101R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000331789
Start	5528688:5528688(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.395T>C
AA Mutation	p.Met132Thr(p.M132T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000331789
Start	5529270:5529270(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.254T>C
AA Mutation	p.Ile85Thr(p.I85T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000331789
Start	5528422:5528422(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.661C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000331789
Start	5529362:5529362(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.162G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000331789
Start	5528085:5528085(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs13447407
CDS Mutation	c.903C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000331789
Start	5529159:5529159(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.363+2T>C
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> ACTB

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000331789
Start	5527812:5527812(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1064T>C
AA Mutation	p.Met355Thr(p.M355T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000331789
Start	5529259:5529259(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.265A>G
AA Mutation	p.Thr89Ala(p.T89A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000331789
Start	5528305:5528305(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.778G>A
AA Mutation	p.Ala260Thr(p.A260T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript