Colon Cancer: Gene >> PAG1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000220597
Start	80985151:80985151(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.501G>T
AA Mutation	p.Lys167Asn(p.K167N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000220597
Start	80976677:80976677(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372766293
CDS Mutation	c.1166C>T
AA Mutation	p.Ala389Val(p.A389V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000220597
Start	80984943:80984943(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368958078
CDS Mutation	c.709C>T
AA Mutation	p.Arg237Cys(p.R237C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000220597
Start	80985013:80985013(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.639C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000220597
Start	80984815:80984815(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200109010
CDS Mutation	c.837G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000220597
Start	80993180:80993180(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.48C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000220597
Start	80976832:80976832(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs151123399
CDS Mutation	c.1011G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> PAG1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000220597
Start	80985237:80985237(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.415G>A
AA Mutation	p.Glu139Lys(p.E139K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000220597
Start	80991516:80991516(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770770967
CDS Mutation	c.140G>A
AA Mutation	p.Arg47Gln(p.R47Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000220597
Start	80993218:80993218(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs151324516
CDS Mutation	c.10G>A
AA Mutation	p.Ala4Thr(p.A4T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000220597
Start	80993106:80993106(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760035686
CDS Mutation	c.122A>G
AA Mutation	p.Asp41Gly(p.D41G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000220597
Start	80985232:80985232(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.420C>T
Mutation Classification	Silent
Feature Type	Transcript