Colon Cancer: Gene >> CTTN

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000301843
Start	70414551:70414551(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777502801
CDS Mutation	c.301G>A
AA Mutation	p.Gly101Ser(p.G101S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000301843
Start	70414609:70414609(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.359G>T
AA Mutation	p.Gly120Val(p.G120V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000301843
Start	70414647:70414647(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.397G>T
AA Mutation	p.Asp133Tyr(p.D133Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000301843
Start	70417101:70417101(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs542706268
CDS Mutation	c.546G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000301843
Start	70431217:70431217(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1203G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000301843
Start	70435102:70435102(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200713620
CDS Mutation	c.1593C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000301843
Start	70435090:70435090(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772572367
CDS Mutation	c.1581C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000301843
Start	70414568:70414568(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.318G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000301843
Start	70407345:70407345(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.48C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> CTTN

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000301843
Start	70433668:70433668(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1466A>G
AA Mutation	p.Tyr489Cys(p.Y489C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000301843
Start	70407345:70407345(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.48C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000301843
Start	70431217:70431217(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1203G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000301843
Start	70419762:70419762(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760754072
CDS Mutation	c.585C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000301843
Start	70433669:70433669(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138763797
CDS Mutation	c.1467C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000301843
Start	70420456:70420460(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.736_740delTGTGC
AA Mutation	p.Cys246ProfsTer13(p.C246Pfs*13)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript