Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> UGT1A9

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000354728
Start	233672242:233672242(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs555995846
CDS Mutation	c.308G>A
AA Mutation	p.Arg103Gln(p.R103Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000354728
Start	233672695:233672695(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375970481
CDS Mutation	c.761G>A
AA Mutation	p.Arg254Gln(p.R254Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000354728
Start	233672698:233672698(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368960201
CDS Mutation	c.764C>T
AA Mutation	p.Thr255Met(p.T255M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000354728
Start	233672763:233672763(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.829T>C
AA Mutation	p.Cys277Arg(p.C277R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000354728
Start	233672007:233672007(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.73G>A
AA Mutation	p.Ala25Thr(p.A25T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000354728
Start	233672180:233672180(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.246C>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> UGT1A9

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000354728
Start	233672062:233672062(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144147859
CDS Mutation	c.128C>T
AA Mutation	p.Ser43Leu(p.S43L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000354728
Start	233672695:233672695(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375970481
CDS Mutation	c.761G>A
AA Mutation	p.Arg254Gln(p.R254Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000354728
Start	233672599:233672599(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772418161
CDS Mutation	c.665G>A
AA Mutation	p.Arg222His(p.R222H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000354728
Start	233672358:233672358(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.424T>G
AA Mutation	p.Phe142Val(p.F142V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript