Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> CA8

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000317995
Start	60222677:60222677(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs387906598
CDS Mutation	c.710G>A
AA Mutation	p.Arg237Gln(p.R237Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000317995
Start	60279790:60279790(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.191C>T
AA Mutation	p.Ser64Leu(p.S64L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000317995
Start	60266028:60266028(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.314C>A
AA Mutation	p.Pro105His(p.P105H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000317995
Start	60232307:60232307(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746839542
CDS Mutation	c.490G>A
AA Mutation	p.Ala164Thr(p.A164T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000317995
Start	60208883:60208883(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.775G>A
AA Mutation	p.Gly259Arg(p.G259R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000317995
Start	60266002:60266002(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201131573
CDS Mutation	c.340G>A
AA Mutation	p.Glu114Lys(p.E114K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000317995
Start	60208834:60208834(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.824G>A
AA Mutation	p.Arg275Gln(p.R275Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000317995
Start	60266042:60266042(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749173414
CDS Mutation	c.300G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> CA8

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000317995
Start	60222677:60222677(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs387906598
CDS Mutation	c.710G>A
AA Mutation	p.Arg237Gln(p.R237Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000317995
Start	60265968:60265968(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200882621
CDS Mutation	c.374G>A
AA Mutation	p.Arg125His(p.R125H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript