Colon Cancer: Gene >> DEGS1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000323699
Start	224189660:224189660(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.166G>A
AA Mutation	p.Gly56Ser(p.G56S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000323699
Start	224190092:224190092(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.598A>G
AA Mutation	p.Ile200Val(p.I200V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000323699
Start	224192470:224192470(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.964C>A
AA Mutation	p.Leu322Met(p.L322M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000323699
Start	224189891:224189891(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.397C>T
AA Mutation	p.Arg133Trp(p.R133W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000323699
Start	224190042:224190042(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs184105229
CDS Mutation	c.548C>T
AA Mutation	p.Thr183Met(p.T183M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> DEGS1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000323699
Start	224189837:224189837(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.343C>T
AA Mutation	p.Pro115Ser(p.P115S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000323699
Start	224190012:224190012(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.518G>A
AA Mutation	p.Arg173Gln(p.R173Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript