Colon Cancer: Gene >> ECI1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000301729
Start	2243145:2243145(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.643G>A
AA Mutation	p.Ala215Thr(p.A215T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000301729
Start	2243214:2243214(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.574A>G
AA Mutation	p.Thr192Ala(p.T192A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000301729
Start	2243104:2243104(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs562082375
CDS Mutation	c.684G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000301729
Start	2243146:2243146(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776709883
CDS Mutation	c.642G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000301729
Start	2240102:2240102(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201856225
CDS Mutation	c.786G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000301729
Start	2244450:2244450(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.397C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	stop_gained
Transcription ID	ENST00000301729
Start	2240113:2240113(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746451005
CDS Mutation	c.775C>T
AA Mutation	p.Arg259Ter(p.R259*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> ECI1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000301729
Start	2239988:2239988(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.900A>C
AA Mutation	p.Glu300Asp(p.E300D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000301729
Start	2243350:2243350(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.531T>C
Mutation Classification	Silent
Feature Type	Transcript