Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> UGT1A8

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000373450
Start	233618350:233618350(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.643G>A
AA Mutation	p.Glu215Lys(p.E215K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000373450
Start	233618248:233618248(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.541G>A
AA Mutation	p.Ala181Thr(p.A181T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373450
Start	233618208:233618208(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.501C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373450
Start	233617785:233617785(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.78G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000373450
Start	233617859:233617859(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.156delG
AA Mutation	p.His53MetfsTer5(p.H53Mfs*5)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000373450
Start	233618052:233618052(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.351delT
AA Mutation	p.Phe117LeufsTer17(p.F117Lfs*17)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	stop_gained
Transcription ID	ENST00000373450
Start	233618014:233618014(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.307C>T
AA Mutation	p.Arg103Ter(p.R103*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> UGT1A8

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000373450
Start	233618191:233618191(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.484T>G
AA Mutation	p.Ser162Ala(p.S162A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000373450
Start	233618051:233618051(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.344G>T
AA Mutation	p.Gly115Val(p.G115V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373450
Start	233618076:233618076(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.369T>C
Mutation Classification	Silent
Feature Type	Transcript