Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> EXOC8

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000366645
Start	231337069:231337069(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.677G>A
AA Mutation	p.Arg226His(p.R226H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000366645
Start	231336416:231336416(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1330C>T
AA Mutation	p.Arg444Cys(p.R444C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000366645
Start	231336175:231336175(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1571T>C
AA Mutation	p.Val524Ala(p.V524A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000366645
Start	231336511:231336511(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1235G>A
AA Mutation	p.Arg412His(p.R412H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000366645
Start	231337168:231337168(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.578A>G
AA Mutation	p.Asp193Gly(p.D193G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_gained
Transcription ID	ENST00000366645
Start	231336584:231336584(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1162C>T
AA Mutation	p.Arg388Ter(p.R388*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> EXOC8

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000366645
Start	231335970:231335970(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1776G>C
AA Mutation	p.Glu592Asp(p.E592D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000366645
Start	231336519:231336519(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1227G>T
AA Mutation	p.Lys409Asn(p.K409N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000366645
Start	231336314:231336314(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1432T>G
AA Mutation	p.Phe478Val(p.F478V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	stop_gained
Transcription ID	ENST00000366645
Start	231336584:231336584(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1162C>T
AA Mutation	p.Arg388Ter(p.R388*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	stop_gained
Transcription ID	ENST00000366645
Start	231336881:231336881(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.865C>T
AA Mutation	p.Arg289Ter(p.R289*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript