Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> TNFRSF10B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000276431
Start	23027278:23027278(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.791G>A
AA Mutation	p.Arg264Gln(p.R264Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000276431
Start	23022805:23022805(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1189G>A
AA Mutation	p.Ala397Thr(p.A397T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000276431
Start	23030779:23030779(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs529765232
CDS Mutation	c.344G>A
AA Mutation	p.Arg115His(p.R115H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000276431
Start	23028533:23028536(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.543_546delAGAA
AA Mutation	p.Lys181AsnfsTer17(p.K181Nfs*17)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	stop_gained
Transcription ID	ENST00000276431
Start	23028535:23028535(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.544G>T
AA Mutation	p.Glu182Ter(p.E182*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> TNFRSF10B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000276431
Start	23029623:23029623(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.463A>G
AA Mutation	p.Lys155Glu(p.K155E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000276431
Start	23028550:23028550(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139403599
CDS Mutation	c.529G>A
AA Mutation	p.Glu177Lys(p.E177K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000276431
Start	23029668:23029668(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761287157
CDS Mutation	c.418G>A
AA Mutation	p.Glu140Lys(p.E140K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	stop_gained
Transcription ID	ENST00000276431
Start	23027249:23027249(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.820G>T
AA Mutation	p.Glu274Ter(p.E274*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript