Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> MTA3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000405094
Start	42579153:42579153(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766940790
CDS Mutation	c.143G>A
AA Mutation	p.Arg48Gln(p.R48Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000405094
Start	42570461:42570461(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.53C>A
AA Mutation	p.Ser18Tyr(p.S18Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000405094
Start	42682407:42682407(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.709G>A
AA Mutation	p.Ala237Thr(p.A237T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000405094
Start	42656279:42656279(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.579T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000405094
Start	42704251:42704251(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1083T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000405094
Start	42682549:42682549(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.855delA
AA Mutation	p.Lys285AsnfsTer19(p.K285Nfs*19)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000405094
Start	42708935:42708936(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1364_1365insATTACTG
AA Mutation	p.Gly456LeufsTer48(p.G456Lfs*48)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> MTA3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000405094
Start	42704207:42704207(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1039C>T
AA Mutation	p.Pro347Ser(p.P347S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000405094
Start	42708885:42708885(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1314T>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000405094
Start	42609540:42609540(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.273C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000405094
Start	42695791:42695792(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.919dupA
AA Mutation	p.Ile307AsnfsTer2(p.I307Nfs*2)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript