Colon Cancer: Gene >> TMEM25

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000313236
Start	118533133:118533133(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377765778
CDS Mutation	c.599G>A
AA Mutation	p.Arg200His(p.R200H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000313236
Start	118532303:118532303(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.224G>A
AA Mutation	p.Ser75Asn(p.S75N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000313236
Start	118533452:118533452(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.706C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000313236
Start	118533454:118533454(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.708G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000313236
Start	118534562:118534562(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1083T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000313236
Start	118532245:118532245(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.171delG
AA Mutation	p.Pro58LeufsTer23(p.P58Lfs*23)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000313236
Start	118532152:118532153(version: GRCh38)
Mutation Type	INS
dbSNP_RS	rs782404272
CDS Mutation	c.79dupG
AA Mutation	p.Glu27GlyfsTer13(p.E27Gfs*13)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> TMEM25

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000313236
Start	118532992:118532992(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs75184401
CDS Mutation	c.458C>T
AA Mutation	p.Ala153Val(p.A153V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript