Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> CYP2U1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000332884
Start	107945402:107945402(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.923C>A
AA Mutation	p.Ser308Tyr(p.S308Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000332884
Start	107945059:107945059(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.580A>C
AA Mutation	p.Ser194Arg(p.S194R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000332884
Start	107945595:107945595(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373823906
CDS Mutation	c.1116C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000332884
Start	107945351:107945351(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.875delA
AA Mutation	p.Lys292ArgfsTer3(p.K292Rfs*3)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000332884
Start	107945487:107945487(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1011delT
AA Mutation	p.Phe337LeufsTer34(p.F337Lfs*34)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> CYP2U1

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000332884
Start	107932054:107932054(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.411C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000332884
Start	107945325:107945325(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.846A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000332884
Start	107949487:107949487(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1431delA
AA Mutation	p.Glu478LysfsTer8(p.E478Kfs*8)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript