Colon Cancer: Gene >> EIF3D

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000216190
Start	36520661:36520661(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771870770
CDS Mutation	c.493C>T
AA Mutation	p.Arg165Cys(p.R165C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000216190
Start	36516721:36516721(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771000513
CDS Mutation	c.1060G>A
AA Mutation	p.Ala354Thr(p.A354T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000216190
Start	36511767:36511767(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774999741
CDS Mutation	c.1369G>A
AA Mutation	p.Val457Met(p.V457M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000216190
Start	36523228:36523228(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.446A>T
AA Mutation	p.Lys149Ile(p.K149I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000216190
Start	36517363:36517363(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745920273
CDS Mutation	c.928C>T
AA Mutation	p.Arg310Cys(p.R310C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000216190
Start	36516770:36516770(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376900932
CDS Mutation	c.1011C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000216190
Start	36526101:36526101(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776873893
CDS Mutation	c.21C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000216190
Start	36519483:36519483(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765560023
CDS Mutation	c.633G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	stop_gained
Transcription ID	ENST00000216190
Start	36523271:36523271(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.403C>T
AA Mutation	p.Arg135Ter(p.R135*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	stop_gained
Transcription ID	ENST00000216190
Start	36524613:36524613(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.289C>T
AA Mutation	p.Arg97Ter(p.R97*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> EIF3D

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000216190
Start	36512527:36512527(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1282A>G
AA Mutation	p.Asn428Asp(p.N428D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript