Colon Cancer: Gene >> MYEOV

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000308946
Start	69295937:69295937(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.487G>A
AA Mutation	p.Ala163Thr(p.A163T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000308946
Start	69295837:69295837(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.387C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000308946
Start	69296257:69296257(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs552116583
CDS Mutation	c.813delG
AA Mutation	p.Trp272GlyfsTer66(p.W272Gfs*66)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000308946
Start	69296256:69296257(version: GRCh38)
Mutation Type	INS
dbSNP_RS	rs761945376
CDS Mutation	c.813dupG
AA Mutation	p.Trp272ValfsTer6(p.W272Vfs*6)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> MYEOV

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000308946
Start	69296027:69296027(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.577G>A
AA Mutation	p.Glu193Lys(p.E193K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000308946
Start	69296257:69296257(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs552116583
CDS Mutation	c.813delG
AA Mutation	p.Trp272GlyfsTer66(p.W272Gfs*66)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript