Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> BUB1B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000287598
Start	40220594:40220594(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2988C>A
AA Mutation	p.Phe996Leu(p.F996L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000287598
Start	40185336:40185336(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.923T>C
AA Mutation	p.Leu308Pro(p.L308P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000287598
Start	40165058:40165058(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.41C>T
AA Mutation	p.Ala14Val(p.A14V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000287598
Start	40210176:40210176(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142705245
CDS Mutation	c.2351C>T
AA Mutation	p.Ala784Val(p.A784V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000287598
Start	40196732:40196732(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1246C>T
AA Mutation	p.Arg416Trp(p.R416W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000287598
Start	40220718:40220718(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3112G>A
AA Mutation	p.Val1038Ile(p.V1038I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000287598
Start	40218495:40218495(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2890T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000287598
Start	40170624:40170624(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.327A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000287598
Start	40210192:40210192(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2367A>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000287598
Start	40206213:40206213(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759148358
CDS Mutation	c.1764C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> BUB1B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000287598
Start	40196673:40196673(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1187T>G
AA Mutation	p.Met396Arg(p.M396R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000287598
Start	40212601:40212601(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2488G>T
AA Mutation	p.Asp830Tyr(p.D830Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000287598
Start	40220594:40220594(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2988C>A
AA Mutation	p.Phe996Leu(p.F996L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000287598
Start	40170638:40170638(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.341G>A
AA Mutation	p.Arg114Gln(p.R114Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript