Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> BIRC2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000227758
Start	102349916:102349916(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.62T>C
AA Mutation	p.Ile21Thr(p.I21T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000227758
Start	102350665:102350665(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.811G>A
AA Mutation	p.Ala271Thr(p.A271T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000227758
Start	102350612:102350612(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.758C>A
AA Mutation	p.Ser253Tyr(p.S253Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000227758
Start	102350928:102350928(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.980C>T
AA Mutation	p.Ala327Val(p.A327V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000227758
Start	102350308:102350308(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.454T>C
AA Mutation	p.Ser152Pro(p.S152P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> BIRC2

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000227758
Start	102377857:102377857(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1622T>C
AA Mutation	p.Val541Ala(p.V541A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000227758
Start	102378163:102378163(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1837G>A
AA Mutation	p.Val613Ile(p.V613I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000227758
Start	102377513:102377513(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779124253
CDS Mutation	c.1384C>T
AA Mutation	p.Arg462Trp(p.R462W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000227758
Start	102368505:102368505(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1323A>C
AA Mutation	p.Lys441Asn(p.K441N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript