Colon Cancer: Gene >> CA7

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000338437
Start	66851520:66851520(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.415G>T
AA Mutation	p.Ala139Ser(p.A139S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000338437
Start	66847062:66847062(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.73G>A
AA Mutation	p.Ala25Thr(p.A25T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000338437
Start	66851548:66851548(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.449delT
AA Mutation	p.Leu150TrpfsTer10(p.L150Wfs*10)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000338437
Start	66851547:66851548(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.449dupT
AA Mutation	p.Leu150PhefsTer58(p.L150Ffs*58)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	protein_altering_variant
Transcription ID	ENST00000338437
Start	66851676:66851677(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.466_467insGAT
AA Mutation	p.His156delinsArgTyr(p.H156delinsRY)
Mutation Classification	In_Frame_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> CA7

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000338437
Start	66852789:66852789(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.594C>T
Mutation Classification	Silent
Feature Type	Transcript