Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> ZYX

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000322764
Start	143383036:143383036(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.737C>A
AA Mutation	p.Ser246Tyr(p.S246Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000322764
Start	143382359:143382359(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.320C>T
AA Mutation	p.Ala107Val(p.A107V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000322764
Start	143388560:143388560(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1216C>T
AA Mutation	p.His406Tyr(p.H406Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000322764
Start	143389935:143389935(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1572C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000322764
Start	143389878:143389878(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142687371
CDS Mutation	c.1515C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_gained
Transcription ID	ENST00000322764
Start	143389927:143389927(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750192633
CDS Mutation	c.1564C>T
AA Mutation	p.Arg522Ter(p.R522*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> ZYX

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000322764
Start	143389879:143389879(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs569088357
CDS Mutation	c.1516G>A
AA Mutation	p.Val506Ile(p.V506I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000322764
Start	143383111:143383111(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.812C>A
AA Mutation	p.Pro271His(p.P271H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000322764
Start	143382837:143382837(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.538C>A
AA Mutation	p.Pro180Thr(p.P180T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000322764
Start	143388871:143388871(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146983863
CDS Mutation	c.1419C>T
Mutation Classification	Silent
Feature Type	Transcript