Colon Cancer: Gene >> SYT13

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000020926
Start	45246509:45246509(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.850C>T
AA Mutation	p.Pro284Ser(p.P284S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000020926
Start	45244089:45244089(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142224925
CDS Mutation	c.1244G>A
AA Mutation	p.Arg415His(p.R415H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000020926
Start	45252563:45252563(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.704C>A
AA Mutation	p.Pro235His(p.P235H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000020926
Start	45255787:45255787(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.288C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000020926
Start	45252607:45252607(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.660C>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> SYT13

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000020926
Start	45244256:45244256(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1077G>T
AA Mutation	p.Met359Ile(p.M359I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000020926
Start	45252444:45252444(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.823G>A
AA Mutation	p.Gly275Ser(p.G275S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript