Colon Cancer: Gene >> GLT1D1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000442111
Start	128899246:128899246(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768702559
CDS Mutation	c.334G>A
AA Mutation	p.Ala112Thr(p.A112T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000442111
Start	128947408:128947408(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759619312
CDS Mutation	c.730G>A
AA Mutation	p.Ala244Thr(p.A244T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000442111
Start	128899262:128899262(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.350T>C
AA Mutation	p.Met117Thr(p.M117T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	stop_gained
Transcription ID	ENST00000442111
Start	128947351:128947351(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.673C>T
AA Mutation	p.Arg225Ter(p.R225*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> GLT1D1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000442111
Start	128888681:128888681(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.260T>C
AA Mutation	p.Val87Ala(p.V87A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	stop_gained
Transcription ID	ENST00000442111
Start	128947375:128947375(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.697G>T
AA Mutation	p.Glu233Ter(p.E233*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript