Colon Cancer: Gene >> SNAP25

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000254976
Start	10296998:10296998(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.355C>T
AA Mutation	p.Arg119Cys(p.R119C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000254976
Start	10293252:10293252(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs1051284
CDS Mutation	c.255C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000254976
Start	10293165:10293165(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.168A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000254976
Start	10296946:10296947(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.309dupA
AA Mutation	p.Ala104SerfsTer5(p.A104Sfs*5)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> SNAP25

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000254976
Start	10296953:10296953(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.310G>T
AA Mutation	p.Ala104Ser(p.A104S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000254976
Start	10275538:10275538(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760339630
CDS Mutation	c.47G>A
AA Mutation	p.Arg16Gln(p.R16Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000254976
Start	10299322:10299322(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201639889
CDS Mutation	c.462C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000254976
Start	10296943:10296943(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.300T>G
Mutation Classification	Silent
Feature Type	Transcript