Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> PYGO1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000302000
Start	55588809:55588809(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.44C>T
AA Mutation	p.Ser15Leu(p.S15L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000302000
Start	55546745:55546745(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.538C>T
AA Mutation	p.Pro180Ser(p.P180S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000302000
Start	55546459:55546459(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.824A>G
AA Mutation	p.Asn275Ser(p.N275S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000302000
Start	55546872:55546872(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.411C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	stop_gained
Transcription ID	ENST00000302000
Start	55546361:55546361(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.922C>T
AA Mutation	p.Arg308Ter(p.R308*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> PYGO1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000302000
Start	55546844:55546844(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.439A>G
AA Mutation	p.Asn147Asp(p.N147D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000302000
Start	55546450:55546450(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200070647
CDS Mutation	c.833G>A
AA Mutation	p.Arg278Gln(p.R278Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000302000
Start	55548916:55548916(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.129T>C
Mutation Classification	Silent
Feature Type	Transcript