Colon Cancer: Gene >> SUCLG1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000393868
Start	84441073:84441073(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.563G>A
AA Mutation	p.Gly188Asp(p.G188D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000393868
Start	84425525:84425525(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.904G>A
AA Mutation	p.Ala302Thr(p.A302T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000393868
Start	84459257:84459257(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.13C>A
AA Mutation	p.Leu5Ile(p.L5I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> SUCLG1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000393868
Start	84431612:84431612(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145106503
CDS Mutation	c.721G>A
AA Mutation	p.Glu241Lys(p.E241K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000393868
Start	84431514:84431514(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.819T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000393868
Start	84425424:84425424(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371224605
CDS Mutation	c.1005G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	stop_gained
Transcription ID	ENST00000393868
Start	84431585:84431585(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.748G>T
AA Mutation	p.Glu250Ter(p.E250*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript