Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> BIRC3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000263464
Start	102325341:102325341(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.832A>C
AA Mutation	p.Ser278Arg(p.S278R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000263464
Start	102336055:102336055(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145025961
CDS Mutation	c.1414G>A
AA Mutation	p.Gly472Arg(p.G472R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000263464
Start	102324739:102324739(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.230A>G
AA Mutation	p.Lys77Arg(p.K77R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000263464
Start	102325144:102325144(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.635T>C
AA Mutation	p.Leu212Ser(p.L212S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000263464
Start	102336769:102336769(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1589A>G
AA Mutation	p.Asp530Gly(p.D530G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000263464
Start	102325014:102325014(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.505G>A
AA Mutation	p.Glu169Lys(p.E169K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000263464
Start	102324852:102324852(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.343T>G
AA Mutation	p.Ser115Ala(p.S115A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	stop_gained
Transcription ID	ENST00000263464
Start	102336977:102336977(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1690G>T
AA Mutation	p.Glu564Ter(p.E564*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> BIRC3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000263464
Start	102324664:102324664(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762397304
CDS Mutation	c.155G>A
AA Mutation	p.Arg52His(p.R52H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000263464
Start	102324529:102324529(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.20G>T
AA Mutation	p.Ser7Ile(p.S7I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000263464
Start	102325024:102325024(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.515G>T
AA Mutation	p.Arg172Ile(p.R172I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000263464
Start	102325110:102325110(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.601G>T
AA Mutation	p.Asp201Tyr(p.D201Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	stop_gained
Transcription ID	ENST00000263464
Start	102336121:102336121(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1480G>T
AA Mutation	p.Glu494Ter(p.E494*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_gained
Transcription ID	ENST00000263464
Start	102337098:102337098(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1811C>A
AA Mutation	p.Ser604Ter(p.S604*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	stop_gained
Transcription ID	ENST00000263464
Start	102331019:102331019(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1102G>T
AA Mutation	p.Glu368Ter(p.E368*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript