Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> TNFSF13B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000375887
Start	108270076:108270076(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.181C>A
AA Mutation	p.Leu61Ile(p.L61I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000375887
Start	108269929:108269932(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.37_40delACTT
AA Mutation	p.Thr13LeufsTer9(p.T13Lfs*9)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000375887
Start	108303348:108303348(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.582delT
AA Mutation	p.Phe194LeufsTer18(p.F194Lfs*18)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	stop_gained
Transcription ID	ENST00000375887
Start	108303526:108303526(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.667G>T
AA Mutation	p.Glu223Ter(p.E223*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	stop_gained
Transcription ID	ENST00000375887
Start	108303550:108303550(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.691C>T
AA Mutation	p.Arg231Ter(p.R231*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_gained
Transcription ID	ENST00000375887
Start	108270418:108270418(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.418G>T
AA Mutation	p.Glu140Ter(p.E140*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> TNFSF13B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000375887
Start	108286855:108286855(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.477A>C
AA Mutation	p.Gln159His(p.Q159H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000375887
Start	108269975:108269975(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.80G>A
AA Mutation	p.Cys27Tyr(p.C27Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000375887
Start	108269957:108269957(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.62A>G
AA Mutation	p.Glu21Gly(p.E21G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000375887
Start	108303357:108303357(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.586T>C
AA Mutation	p.Tyr196His(p.Y196H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	stop_gained
Transcription ID	ENST00000375887
Start	108306876:108306876(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.796G>T
AA Mutation	p.Glu266Ter(p.E266*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript