Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> BAMBI

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000375533
Start	28682287:28682287(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.669G>T
AA Mutation	p.Glu223Asp(p.E223D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000375533
Start	28681294:28681294(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.113T>C
AA Mutation	p.Val38Ala(p.V38A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000375533
Start	28681347:28681347(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375455762
CDS Mutation	c.166C>A
AA Mutation	p.Leu56Ile(p.L56I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000375533
Start	28682076:28682076(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776749607
CDS Mutation	c.458C>T
AA Mutation	p.Ala153Val(p.A153V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000375533
Start	28682148:28682148(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369743386
CDS Mutation	c.530G>A
AA Mutation	p.Arg177Gln(p.R177Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_gained
Transcription ID	ENST00000375533
Start	28681437:28681437(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772888888
CDS Mutation	c.256C>T
AA Mutation	p.Arg86Ter(p.R86*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> BAMBI

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000375533
Start	28682148:28682148(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369743386
CDS Mutation	c.530G>A
AA Mutation	p.Arg177Gln(p.R177Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000375533
Start	28681315:28681315(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.134A>C
AA Mutation	p.Lys45Thr(p.K45T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	stop_gained
Transcription ID	ENST00000375533
Start	28682147:28682147(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.529C>T
AA Mutation	p.Arg177Ter(p.R177*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript