Colon Cancer: Gene >> CYTL1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000307746
Start	5019327:5019327(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.119G>A
AA Mutation	p.Arg40His(p.R40H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000307746
Start	5015176:5015176(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200085707
CDS Mutation	c.386C>T
AA Mutation	p.Thr129Met(p.T129M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000307746
Start	5016869:5016869(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.294G>T
AA Mutation	p.Lys98Asn(p.K98N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000307746
Start	5019383:5019383(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.63G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000307746
Start	5019341:5019341(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.105C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_gained
Transcription ID	ENST00000307746
Start	5016959:5016959(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.204C>A
AA Mutation	p.Tyr68Ter(p.Y68*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> CYTL1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000307746
Start	5017142:5017142(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.191A>G
AA Mutation	p.Asp64Gly(p.D64G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript