Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> TRIB2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000155926
Start	12740702:12740702(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376273712
CDS Mutation	c.940G>A
AA Mutation	p.Val314Ile(p.V314I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000155926
Start	12740770:12740770(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1008G>T
AA Mutation	p.Glu336Asp(p.E336D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000155926
Start	12740393:12740393(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.631G>A
AA Mutation	p.Asp211Asn(p.D211N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000155926
Start	12723524:12723524(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.535C>T
AA Mutation	p.Arg179Trp(p.R179W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000155926
Start	12723337:12723337(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.348C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000155926
Start	12723544:12723544(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144779580
CDS Mutation	c.555C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000155926
Start	12740749:12740749(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373997699
CDS Mutation	c.987G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000155926
Start	12740707:12740707(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369596172
CDS Mutation	c.945G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000155926
Start	12740596:12740596(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767201347
CDS Mutation	c.834G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> TRIB2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000155926
Start	12740513:12740513(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs186204534
CDS Mutation	c.751C>T
AA Mutation	p.Arg251Trp(p.R251W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000155926
Start	12740714:12740714(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.952G>A
AA Mutation	p.Ala318Thr(p.A318T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000155926
Start	12723545:12723545(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs546825227
CDS Mutation	c.556G>A
AA Mutation	p.Glu186Lys(p.E186K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000155926
Start	12740468:12740468(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.706G>A
AA Mutation	p.Asp236Asn(p.D236N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000155926
Start	12718536:12718536(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.229C>T
AA Mutation	p.Arg77Cys(p.R77C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000155926
Start	12723493:12723493(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs542940298
CDS Mutation	c.504C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000155926
Start	12740707:12740707(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369596172
CDS Mutation	c.945G>A
Mutation Classification	Silent
Feature Type	Transcript