Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> AGK

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000355413
Start	141651533:141651533(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1055A>C
AA Mutation	p.Lys352Thr(p.K352T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000355413
Start	141555492:141555492(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs577821330
CDS Mutation	c.26G>A
AA Mutation	p.Arg9Gln(p.R9Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000355413
Start	141615525:141615525(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.478T>G
AA Mutation	p.Leu160Val(p.L160V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000355413
Start	141633901:141633901(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.589G>T
AA Mutation	p.Gly197Cys(p.G197C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000355413
Start	141596567:141596567(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.147T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000355413
Start	141593167:141593167(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.123A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000355413
Start	141652786:141652786(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1132-1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> AGK

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000355413
Start	141641272:141641272(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.751T>C
AA Mutation	p.Ser251Pro(p.S251P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000355413
Start	141641369:141641369(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.848T>C
AA Mutation	p.Leu283Pro(p.L283P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000355413
Start	141633942:141633942(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.630A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000355413
Start	141621798:141621798(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.585C>A
Mutation Classification	Silent
Feature Type	Transcript