Colon Cancer: Gene >> CD3EAP

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000309424
Start	45408984:45408984(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778451525
CDS Mutation	c.1016T>C
AA Mutation	p.Met339Thr(p.M339T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000309424
Start	45408173:45408173(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778171085
CDS Mutation	c.205G>A
AA Mutation	p.Val69Ile(p.V69I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000309424
Start	45408455:45408455(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.487T>A
AA Mutation	p.Ser163Thr(p.S163T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000309424
Start	45408582:45408582(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.614C>T
AA Mutation	p.Ser205Leu(p.S205L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000309424
Start	45408999:45408999(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146750944
CDS Mutation	c.1031C>T
AA Mutation	p.Thr344Met(p.T344M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> CD3EAP

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000309424
Start	45408142:45408142(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.174G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000309424
Start	45408512:45408512(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.544delA
AA Mutation	p.Thr182GlnfsTer10(p.T182Qfs*10)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript