Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> RUNDC3A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000426726
Start	44316696:44316696(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1169C>T
AA Mutation	p.Thr390Met(p.T390M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000426726
Start	44314978:44314978(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754541765
CDS Mutation	c.598G>A
AA Mutation	p.Asp200Asn(p.D200N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000426726
Start	44315306:44315306(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.781G>A
AA Mutation	p.Val261Ile(p.V261I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000426726
Start	44316637:44316637(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1110G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000426726
Start	44312625:44312625(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.153C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000426726
Start	44315191:44315191(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.666C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	start_lost
Transcription ID	ENST00000426726
Start	44308835:44308835(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3G>A
AA Mutation	p.Met1?(p.M1?)
Mutation Classification	Translation_Start_Site
Feature Type	Transcript

Rectum Cancer: Gene >> RUNDC3A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000426726
Start	44315581:44315581(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.925G>T
AA Mutation	p.Gly309Cys(p.G309C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000426726
Start	44316420:44316420(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.989C>T
AA Mutation	p.Ala330Val(p.A330V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000426726
Start	44312637:44312637(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200736626
CDS Mutation	c.165G>A
Mutation Classification	Silent
Feature Type	Transcript