Colon Cancer: Gene >> RUNX3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000308873
Start	24902307:24902307(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752706729
CDS Mutation	c.1063C>T
AA Mutation	p.Arg355Cys(p.R355C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000308873
Start	24907349:24907349(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.613C>T
AA Mutation	p.Arg205Cys(p.R205C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000308873
Start	24907307:24907307(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.655C>T
AA Mutation	p.Leu219Phe(p.L219F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000399916
Start	24964564:24964564(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs193187661
CDS Mutation	c.8C>T
AA Mutation	p.Ser3Leu(p.S3L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000308873
Start	24929662:24929662(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.207C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000308873
Start	24902320:24902320(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1050C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000308873
Start	24927652:24927652(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.361C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000308873
Start	24927635:24927635(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757662116
CDS Mutation	c.378C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000308873
Start	24902641:24902641(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144597350
CDS Mutation	c.729C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> RUNX3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000308873
Start	24902553:24902553(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.817G>C
AA Mutation	p.Ala273Pro(p.A273P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000308873
Start	24919258:24919258(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.526G>A
AA Mutation	p.Gly176Arg(p.G176R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000308873
Start	24902544:24902544(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.826G>A
AA Mutation	p.Ala276Thr(p.A276T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000308873
Start	24902200:24902200(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs573562275
CDS Mutation	c.1170C>T
Mutation Classification	Silent
Feature Type	Transcript