Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> TNFSF18

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000404377
Start	173050746:173050746(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.217T>A
AA Mutation	p.Leu73Ile(p.L73I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000404377
Start	173050844:173050844(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.119G>A
AA Mutation	p.Gly40Glu(p.G40E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000404377
Start	173050821:173050821(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.142C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000404377
Start	173041667:173041667(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375329121
CDS Mutation	c.300C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000404377
Start	173041419:173041419(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.548delA
AA Mutation	p.Asn183IlefsTer10(p.N183Ifs*10)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> TNFSF18

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000404377
Start	173041555:173041555(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370771974
CDS Mutation	c.412C>T
AA Mutation	p.Arg138Trp(p.R138W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000404377
Start	173050853:173050853(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.110G>T
AA Mutation	p.Arg37Ile(p.R37I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000404377
Start	173041419:173041419(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.548delA
AA Mutation	p.Asn183IlefsTer10(p.N183Ifs*10)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript