Colon Cancer: Gene >> STT3A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000392708
Start	125612662:125612662(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1280C>G
AA Mutation	p.Ser427Cys(p.S427C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000392708
Start	125618385:125618385(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1787T>G
AA Mutation	p.Phe596Cys(p.F596C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000392708
Start	125612692:125612692(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776079118
CDS Mutation	c.1310G>A
AA Mutation	p.Arg437His(p.R437H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000392708
Start	125602826:125602826(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779755051
CDS Mutation	c.295A>G
AA Mutation	p.Ile99Val(p.I99V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000392708
Start	125602843:125602843(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.317delT
AA Mutation	p.Phe106SerfsTer45(p.F106Sfs*45)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_gained
Transcription ID	ENST00000392708
Start	125602409:125602409(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.256G>T
AA Mutation	p.Gly86Ter(p.G86*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	protein_altering_variant
Transcription ID	ENST00000392708
Start	125620121:125620122(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.2074_2075insGGATTCAGG
AA Mutation	p.Tyr692delinsTrpIleGlnAsp(p.Y692delinsWIQD)
Mutation Classification	In_Frame_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> STT3A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000392708
Start	125608232:125608232(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765580288
CDS Mutation	c.904G>A
AA Mutation	p.Val302Ile(p.V302I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000392708
Start	125608233:125608233(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.905T>A
AA Mutation	p.Val302Asp(p.V302D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000392708
Start	125608216:125608216(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.888A>C
AA Mutation	p.Glu296Asp(p.E296D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000392708
Start	125614145:125614145(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1613G>A
AA Mutation	p.Arg538Gln(p.R538Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript