Colon Cancer: Gene >> SYT7

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000263846
Start	61518710:61518710(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1129G>A
AA Mutation	p.Gly377Arg(p.G377R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000263846
Start	61551435:61551435(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755352659
CDS Mutation	c.164C>T
AA Mutation	p.Thr55Met(p.T55M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000263846
Start	61524487:61524487(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.668T>C
AA Mutation	p.Val223Ala(p.V223A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263846
Start	61556197:61556197(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750524510
CDS Mutation	c.42G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263846
Start	61533058:61533058(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765641562
CDS Mutation	c.282C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000263846
Start	61523835:61523835(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.899delG
AA Mutation	p.Gly300AlafsTer7(p.G300Afs*7)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000263846
Start	61523834:61523835(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.899dupG
AA Mutation	p.Thr301HisfsTer35(p.T301Hfs*35)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> SYT7

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000263846
Start	61523136:61523136(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747884194
CDS Mutation	c.1046C>T
AA Mutation	p.Thr349Met(p.T349M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263846
Start	61528084:61528084(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372903756
CDS Mutation	c.453G>A
Mutation Classification	Silent
Feature Type	Transcript