Colon Cancer: Gene >> VSIG2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000326621
Start	124748462:124748462(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs183266468
CDS Mutation	c.779C>T
AA Mutation	p.Ala260Val(p.A260V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000326621
Start	124748478:124748478(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.763T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000326621
Start	124750844:124750844(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.297delC
AA Mutation	p.Thr100GlnfsTer7(p.T100Qfs*7)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> VSIG2

Mutation ID	1
Mutation Consequence	stop_gained
Transcription ID	ENST00000326621
Start	124750913:124750913(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.228C>A
AA Mutation	p.Tyr76Ter(p.Y76*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript