Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> TNFSF4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000281834
Start	173186667:173186667(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.401C>T
AA Mutation	p.Ser134Phe(p.S134F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000281834
Start	173188536:173188536(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.187A>C
AA Mutation	p.Lys63Gln(p.K63Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000281834
Start	173188550:173188550(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368338886
CDS Mutation	c.173G>A
AA Mutation	p.Arg58Gln(p.R58Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000281834
Start	173186645:173186645(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.423C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000281834
Start	173186831:173186831(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.237C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000281834
Start	173186552:173186552(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.516T>C
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> TNFSF4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000281834
Start	173188550:173188550(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368338886
CDS Mutation	c.173G>A
AA Mutation	p.Arg58Gln(p.R58Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000281834
Start	173188521:173188521(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.202G>A
AA Mutation	p.Glu68Lys(p.E68K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000281834
Start	173207169:173207169(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.8G>A
AA Mutation	p.Arg3Lys(p.R3K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000281834
Start	173186730:173186730(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.338T>G
AA Mutation	p.Val113Gly(p.V113G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000281834
Start	173186780:173186780(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.288C>A
AA Mutation	p.Asn96Lys(p.N96K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript