Colon Cancer: Gene >> TMED2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000262225
Start	123596716:123596716(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746703169
CDS Mutation	c.593G>A
AA Mutation	p.Arg198Gln(p.R198Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000262225
Start	123586885:123586885(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.319A>T
AA Mutation	p.Met107Leu(p.M107L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	stop_gained
Transcription ID	ENST00000262225
Start	123584727:123584727(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.91G>T
AA Mutation	p.Glu31Ter(p.E31*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	start_lost
Transcription ID	ENST00000262225
Start	123584639:123584639(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3G>T
AA Mutation	p.Met1?(p.M1?)
Mutation Classification	Translation_Start_Site
Feature Type	Transcript

Rectum Cancer: Gene >> TMED2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000262225
Start	123584767:123584767(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.131G>A
AA Mutation	p.Gly44Asp(p.G44D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000262225
Start	123586745:123586745(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.181-2A>G
Mutation Classification	Splice_Site
Feature Type	Transcript