Colon Cancer: Gene >> TFE3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000315869
Start	49038304:49038304(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.673G>A
AA Mutation	p.Ala225Thr(p.A225T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000315869
Start	49039267:49039267(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782500227
CDS Mutation	c.374C>T
AA Mutation	p.Ala125Val(p.A125V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000315869
Start	49039207:49039207(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.434C>A
AA Mutation	p.Pro145His(p.P145H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000315869
Start	49038415:49038415(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.562C>T
AA Mutation	p.Arg188Cys(p.R188C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000315869
Start	49030223:49030223(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1663G>A
AA Mutation	p.Val555Met(p.V555M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000315869
Start	49031503:49031503(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1178T>C
AA Mutation	p.Val393Ala(p.V393A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000315869
Start	49039228:49039228(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.413C>T
AA Mutation	p.Ala138Val(p.A138V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000315869
Start	49038323:49038323(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373899230
CDS Mutation	c.654A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000315869
Start	49030270:49030270(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1616delG
AA Mutation	p.Gly539ValfsTer209(p.G539Vfs*209)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> TFE3

No Mutation Annotation!