Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> RAP1GAP

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000374765
Start	21617413:21617413(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.184G>A
AA Mutation	p.Glu62Lys(p.E62K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000374765
Start	21598049:21598049(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1895C>A
AA Mutation	p.Pro632His(p.P632H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000374765
Start	21606103:21606103(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201567525
CDS Mutation	c.1391C>T
AA Mutation	p.Ala464Val(p.A464V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000374765
Start	21599607:21599607(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150869374
CDS Mutation	c.1663G>A
AA Mutation	p.Ala555Thr(p.A555T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000374765
Start	21602856:21602856(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1486C>T
AA Mutation	p.Arg496Cys(p.R496C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374765
Start	21608925:21608925(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1083C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374765
Start	21608321:21608321(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1188G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> RAP1GAP

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000374765
Start	21617443:21617443(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.154G>A
AA Mutation	p.Gly52Arg(p.G52R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000374765
Start	21608228:21608228(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1281C>A
AA Mutation	p.Phe427Leu(p.F427L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000374765
Start	21608917:21608917(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1091T>G
AA Mutation	p.Phe364Cys(p.F364C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	stop_gained
Transcription ID	ENST00000374765
Start	21611756:21611756(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.673G>T
AA Mutation	p.Glu225Ter(p.E225*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript