Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> ACCS

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000263776
Start	44077311:44077311(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373138553
CDS Mutation	c.589G>A
AA Mutation	p.Ala197Thr(p.A197T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000263776
Start	44083442:44083442(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1273T>G
AA Mutation	p.Phe425Val(p.F425V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000263776
Start	44083490:44083490(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1321C>A
AA Mutation	p.Leu441Met(p.L441M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000263776
Start	44083307:44083307(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1250G>T
AA Mutation	p.Arg417Ile(p.R417I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263776
Start	44075552:44075552(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764847227
CDS Mutation	c.516G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263776
Start	44083492:44083492(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1323G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263776
Start	44071273:44071273(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.306C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> ACCS

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000263776
Start	44079574:44079574(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.877G>A
AA Mutation	p.Val293Met(p.V293M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000263776
Start	44067682:44067682(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.55A>G
AA Mutation	p.Thr19Ala(p.T19A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000263776
Start	44067830:44067830(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.203G>T
AA Mutation	p.Arg68Ile(p.R68I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000263776
Start	44079618:44079618(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.921A>C
AA Mutation	p.Glu307Asp(p.E307D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000263776
Start	44083220:44083220(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1163C>T
AA Mutation	p.Ala388Val(p.A388V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000263776
Start	44074678:44074678(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.486G>T
AA Mutation	p.Glu162Asp(p.E162D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript