Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> ARMC8

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000469044
Start	138209836:138209836(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.65G>A
AA Mutation	p.Arg22His(p.R22H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000469044
Start	138235054:138235054(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.549T>G
AA Mutation	p.Ile183Met(p.I183M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000469044
Start	138245127:138245127(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1078G>A
AA Mutation	p.Ala360Thr(p.A360T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000469044
Start	138223650:138223650(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.352G>T
AA Mutation	p.Asp118Tyr(p.D118Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000469044
Start	138223686:138223686(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.388C>T
AA Mutation	p.Arg130Cys(p.R130C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000469044
Start	138284456:138284456(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1751C>T
AA Mutation	p.Ala584Val(p.A584V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000469044
Start	138241896:138241896(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765855548
CDS Mutation	c.951C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> ARMC8

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000469044
Start	138264169:138264169(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1256G>A
AA Mutation	p.Arg419Gln(p.R419Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	stop_gained
Transcription ID	ENST00000469044
Start	138264168:138264168(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1255C>T
AA Mutation	p.Arg419Ter(p.R419*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000469044
Start	138241984:138241984(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1038+1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript