Colon Cancer: Gene >> UST

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000367463
Start	149021364:149021364(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755609661
CDS Mutation	c.820G>A
AA Mutation	p.Val274Met(p.V274M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000367463
Start	148747672:148747672(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747844853
CDS Mutation	c.242A>G
AA Mutation	p.Tyr81Cys(p.Y81C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000367463
Start	148964555:148964555(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746546399
CDS Mutation	c.673C>T
AA Mutation	p.Arg225Cys(p.R225C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000367463
Start	149074040:149074040(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1145C>T
AA Mutation	p.Pro382Leu(p.P382L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000367463
Start	149021394:149021394(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.850C>A
AA Mutation	p.Leu284Ile(p.L284I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000367463
Start	149073920:149073920(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1025G>T
AA Mutation	p.Arg342Ile(p.R342I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367463
Start	149021456:149021456(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201497317
CDS Mutation	c.912C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000367463
Start	149074006:149074006(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs766240903
CDS Mutation	c.1117delC
AA Mutation	p.Leu373Ter(p.L373*)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000367463
Start	148747493:148747493(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.68delG
AA Mutation	p.Gly23AlafsTer88(p.G23Afs*88)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	stop_gained
Transcription ID	ENST00000367463
Start	148953923:148953923(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.499C>T
AA Mutation	p.Arg167Ter(p.R167*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> UST

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000367463
Start	149073893:149073893(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.998C>T
AA Mutation	p.Ala333Val(p.A333V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000367463
Start	149021394:149021394(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.850C>A
AA Mutation	p.Leu284Ile(p.L284I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367463
Start	148953925:148953925(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.501A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367463
Start	148941389:148941389(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.402C>T
Mutation Classification	Silent
Feature Type	Transcript