Colon Cancer: Gene >> TM4SF5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000270560
Start	4782894:4782894(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.436G>A
AA Mutation	p.Glu146Lys(p.E146K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000270560
Start	4782979:4782979(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.521G>T
AA Mutation	p.Gly174Val(p.G174V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000270560
Start	4782988:4782988(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199806115
CDS Mutation	c.530T>C
AA Mutation	p.Leu177Pro(p.L177P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000270560
Start	4783016:4783016(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.558C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000270560
Start	4780812:4780812(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781396189
CDS Mutation	c.201C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000270560
Start	4782610:4782610(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.366C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000270560
Start	4782532:4782532(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.288C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000270560
Start	4782607:4782607(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756181828
CDS Mutation	c.363C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000270560
Start	4783028:4783029(version: GRCh38)
Mutation Type	INS
dbSNP_RS	rs780191120
CDS Mutation	c.576dupA
AA Mutation	p.Gln193ThrfsTer10(p.Q193Tfs*10)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> TM4SF5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000270560
Start	4782582:4782582(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.338G>A
AA Mutation	p.Arg113Gln(p.R113Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript