Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> TM9SF4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000398022
Start	32150825:32150825(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750795353
CDS Mutation	c.1195C>T
AA Mutation	p.Arg399Cys(p.R399C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000398022
Start	32157908:32157908(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1444C>T
AA Mutation	p.Arg482Cys(p.R482C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000398022
Start	32155157:32155157(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1300T>C
AA Mutation	p.Phe434Leu(p.F434L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000398022
Start	32155128:32155128(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1275delT
AA Mutation	p.Phe425LeufsTer7(p.F425Lfs*7)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> TM9SF4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000398022
Start	32165427:32165427(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777279514
CDS Mutation	c.1912G>A
AA Mutation	p.Ala638Thr(p.A638T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000398022
Start	32141517:32141517(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.250C>T
AA Mutation	p.Arg84Trp(p.R84W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000398022
Start	32165386:32165386(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1871G>T
AA Mutation	p.Gly624Val(p.G624V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000398022
Start	32141796:32141796(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.429G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000398022
Start	32157853:32157853(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746687547
CDS Mutation	c.1389C>T
Mutation Classification	Silent
Feature Type	Transcript