Colon Cancer: Gene >> CD69

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000228434
Start	9754674:9754674(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.404A>G
AA Mutation	p.Tyr135Cys(p.Y135C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000228434
Start	9756354:9756354(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.130G>C
AA Mutation	p.Ala44Pro(p.A44P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000228434
Start	9756337:9756337(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.147C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000228434
Start	9755227:9755227(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.222C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> CD69

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000228434
Start	9756387:9756387(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.97C>A
AA Mutation	p.His33Asn(p.H33N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000228434
Start	9755229:9755229(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.220T>A
AA Mutation	p.Phe74Ile(p.F74I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000228434
Start	9753547:9753548(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.533dupA
AA Mutation	p.Asn178LysfsTer10(p.N178Kfs*10)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript