Colon Cancer: Gene >> DEGS2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000305631
Start	100149356:100149356(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.437C>G
AA Mutation	p.Thr146Arg(p.T146R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000305631
Start	100149668:100149668(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.125G>A
AA Mutation	p.Arg42His(p.R42H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000305631
Start	100149116:100149116(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765100971
CDS Mutation	c.677C>T
AA Mutation	p.Ser226Leu(p.S226L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000305631
Start	100159549:100159549(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.39C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000305631
Start	100149142:100149142(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.651C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000305631
Start	100148971:100148971(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374265570
CDS Mutation	c.822G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> DEGS2

No Mutation Annotation!