Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> CD40

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000372285
Start	46118351:46118351(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.8G>A
AA Mutation	p.Arg3His(p.R3H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000372285
Start	46128148:46128148(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.570T>A
AA Mutation	p.Asp190Glu(p.D190E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000372285
Start	46122233:46122233(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.131G>T
AA Mutation	p.Gly44Val(p.G44V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000372285
Start	46122626:46122626(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.273C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant;splice_region_variant
Transcription ID	ENST00000372285
Start	46128882:46128883(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.682dupC
AA Mutation	p.His228ProfsTer79(p.H228Pfs*79)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> CD40

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000372285
Start	46126647:46126647(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.505A>C
AA Mutation	p.Thr169Pro(p.T169P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000372285
Start	46122754:46122754(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371997367
CDS Mutation	c.401T>C
AA Mutation	p.Ile134Thr(p.I134T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000372285
Start	46123197:46123197(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.475G>A
AA Mutation	p.Glu159Lys(p.E159K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000372285
Start	46128345:46128345(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.662A>C
AA Mutation	p.Lys221Thr(p.K221T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript