Colon Cancer: Gene >> BFAR

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000261658
Start	14667813:14667813(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1339A>G
AA Mutation	p.Thr447Ala(p.T447A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000261658
Start	14664951:14664951(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1040T>A
AA Mutation	p.Phe347Tyr(p.F347Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000261658
Start	14649882:14649882(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.547A>G
AA Mutation	p.Thr183Ala(p.T183A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000261658
Start	14667801:14667801(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777625063
CDS Mutation	c.1327C>T
AA Mutation	p.Arg443Trp(p.R443W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000261658
Start	14655083:14655083(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.656C>A
AA Mutation	p.Thr219Lys(p.T219K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261658
Start	14648541:14648541(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.417G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261658
Start	14661981:14661981(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.873C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261658
Start	14665021:14665021(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1110A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000261658
Start	14667688:14667688(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1218delT
AA Mutation	p.Phe406LeufsTer52(p.F406Lfs*52)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000261658
Start	14655184:14655184(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.763delC
AA Mutation	p.Gln255ArgfsTer9(p.Q255Rfs*9)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> BFAR

No Mutation Annotation!