Colon Cancer: Gene >> RARA

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000254066
Start	40348409:40348409(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.272G>A
AA Mutation	p.Cys91Tyr(p.C91Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000254066
Start	40355266:40355266(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1016G>A
AA Mutation	p.Arg339His(p.R339H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000254066
Start	40352356:40352356(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.656C>A
AA Mutation	p.Ser219Tyr(p.S219Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000254066
Start	40354446:40354446(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.952C>T
AA Mutation	p.Pro318Ser(p.P318S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000254066
Start	40354332:40354332(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.838G>A
AA Mutation	p.Glu280Lys(p.E280K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000254066
Start	40354308:40354308(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.814C>T
AA Mutation	p.Arg272Trp(p.R272W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000254066
Start	40331287:40331287(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.69C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000254066
Start	40331335:40331335(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767135725
CDS Mutation	c.117C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000254066
Start	40354343:40354343(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.849C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000254066
Start	40354476:40354476(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.982C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000254066
Start	40356118:40356118(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1286delG
AA Mutation	p.Gly429ValfsTer214(p.G429Vfs*214)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000254066
Start	40348371:40348372(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.239dupC
AA Mutation	p.Leu81SerfsTer26(p.L81Sfs*26)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> RARA

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000254066
Start	40352015:40352015(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754292583
CDS Mutation	c.575G>A
AA Mutation	p.Arg192His(p.R192H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript