Colon Cancer: Gene >> SYT1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000261205
Start	79296138:79296138(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.544G>A
AA Mutation	p.Val182Met(p.V182M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000261205
Start	79299522:79299522(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750035344
CDS Mutation	c.781C>T
AA Mutation	p.Arg261Cys(p.R261C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000261205
Start	79296201:79296201(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.607C>A
AA Mutation	p.Leu203Ile(p.L203I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000261205
Start	79353585:79353585(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.894G>T
AA Mutation	p.Lys298Asn(p.K298N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000261205
Start	79217574:79217574(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144005237
CDS Mutation	c.55G>A
AA Mutation	p.Ala19Thr(p.A19T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000261205
Start	79296163:79296163(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.569A>C
AA Mutation	p.Lys190Thr(p.K190T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000261205
Start	79285793:79285793(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.173C>T
AA Mutation	p.Pro58Leu(p.P58L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261205
Start	79285794:79285794(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760435569
CDS Mutation	c.174G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261205
Start	79299479:79299479(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.738C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000261205
Start	79285904:79285904(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.288delA
AA Mutation	p.Gly97GlufsTer8(p.G97Efs*8)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000261205
Start	79299383:79299383(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.643-1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> SYT1

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261205
Start	79296137:79296137(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778647625
CDS Mutation	c.543C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261205
Start	79292046:79292046(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.390T>C
Mutation Classification	Silent
Feature Type	Transcript