Colon Cancer: Gene >> SMURF2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000262435
Start	64551617:64551617(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1836T>G
AA Mutation	p.His612Gln(p.H612Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000262435
Start	64586113:64586113(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781984446
CDS Mutation	c.458G>A
AA Mutation	p.Arg153His(p.R153H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262435
Start	64593513:64593513(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782298029
CDS Mutation	c.261G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262435
Start	64578563:64578563(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs189660096
CDS Mutation	c.786G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262435
Start	64561556:64561556(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1260G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> SMURF2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000262435
Start	64547740:64547740(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1931A>G
AA Mutation	p.Lys644Arg(p.K644R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000262435
Start	64586153:64586153(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.418G>A
AA Mutation	p.Asp140Asn(p.D140N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript