Colon Cancer: Gene >> HMGCL

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374490
Start	23820561:23820561(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.93G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374490
Start	23808291:23808291(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139799938
CDS Mutation	c.594C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374490
Start	23817524:23817524(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.204C>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> HMGCL

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000374490
Start	23820532:23820532(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs121964997
CDS Mutation	c.122G>A
AA Mutation	p.Arg41Gln(p.R41Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000374490
Start	23808229:23808229(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.656C>A
AA Mutation	p.Ser219Tyr(p.S219Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374490
Start	23816711:23816711(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.312A>G
Mutation Classification	Silent
Feature Type	Transcript