Colon Cancer: Gene >> CORO1A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000219150
Start	30185271:30185271(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.62C>T
AA Mutation	p.Ala21Val(p.A21V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000219150
Start	30185403:30185403(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.194G>A
AA Mutation	p.Gly65Asp(p.G65D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000219150
Start	30187812:30187812(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.844G>A
AA Mutation	p.Val282Ile(p.V282I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000219150
Start	30187136:30187136(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.549C>G
AA Mutation	p.Asp183Glu(p.D183E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000219150
Start	30188397:30188397(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1102G>A
AA Mutation	p.Ala368Thr(p.A368T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000219150
Start	30186912:30186912(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.418C>A
AA Mutation	p.His140Asn(p.H140N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000219150
Start	30185371:30185371(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs536390638
CDS Mutation	c.162C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000219150
Start	30186621:30186621(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747607776
CDS Mutation	c.222G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> CORO1A

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000219150
Start	30185371:30185371(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs536390638
CDS Mutation	c.162C>T
Mutation Classification	Silent
Feature Type	Transcript