Colon Cancer: Gene >> GLIS2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000262366
Start	4337072:4337072(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779142808
CDS Mutation	c.1123G>C
AA Mutation	p.Ala375Pro(p.A375P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000262366
Start	4336970:4336970(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1021G>A
AA Mutation	p.Ala341Thr(p.A341T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262366
Start	4337494:4337494(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762142916
CDS Mutation	c.1545G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262366
Start	4337299:4337299(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150464446
CDS Mutation	c.1350G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262366
Start	4335386:4335386(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149145163
CDS Mutation	c.768G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262366
Start	4337071:4337071(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1122G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262366
Start	4336915:4336915(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.966C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000262366
Start	4334870:4334870(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.421delG
AA Mutation	p.Ala141ProfsTer110(p.A141Pfs*110)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000262366
Start	4337132:4337132(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1190delG
AA Mutation	p.Gly397AlafsTer127(p.G397Afs*127)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> GLIS2

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262366
Start	4337509:4337509(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759274279
CDS Mutation	c.1560G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000262366
Start	4334870:4334870(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.421delG
AA Mutation	p.Ala141ProfsTer110(p.A141Pfs*110)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript