Colon Cancer: Gene >> GLUD1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000277865
Start	87068112:87068112(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.692G>A
AA Mutation	p.Arg231Gln(p.R231Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000277865
Start	87053353:87053353(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1546C>T
AA Mutation	p.Arg516Cys(p.R516C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000277865
Start	87060708:87060708(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1177G>A
AA Mutation	p.Ala393Thr(p.A393T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000277865
Start	87094578:87094578(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.192C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000277865
Start	87059202:87059202(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1350C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000277865
Start	87076008:87076008(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.542delG
AA Mutation	p.Gly181ValfsTer29(p.G181Vfs*29)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000277865
Start	87060727:87060728(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1157_1158insCTGTATGGTATGT
AA Mutation	p.Lys386AsnfsTer22(p.K386Nfs*22)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> GLUD1

No Mutation Annotation!