Colon Cancer: Gene >> AK3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000381809
Start	4719220:4719220(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.359T>G
AA Mutation	p.Val120Gly(p.V120G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000381809
Start	4718526:4718526(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.456C>G
AA Mutation	p.Asp152Glu(p.D152E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000381809
Start	4741000:4741000(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.88C>G
AA Mutation	p.His30Asp(p.H30D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000381809
Start	4741076:4741076(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.12C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000381809
Start	4722618:4722618(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752236904
CDS Mutation	c.159C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000381809
Start	4719246:4719246(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777638742
CDS Mutation	c.333G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000381809
Start	4741081:4741081(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.7delG
AA Mutation	p.Ala3ArgfsTer9(p.A3Rfs*9)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> AK3

No Mutation Annotation!