Colon Cancer: Gene >> GFI1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000294702
Start	92482873:92482873(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771344042
CDS Mutation	c.289G>A
AA Mutation	p.Ala97Thr(p.A97T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000294702
Start	92476201:92476201(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1097A>T
AA Mutation	p.Lys366Met(p.K366M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000294702
Start	92478689:92478689(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.989A>C
AA Mutation	p.His330Pro(p.H330P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000294702
Start	92483427:92483427(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.61C>A
AA Mutation	p.Pro21Thr(p.P21T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000294702
Start	92476048:92476048(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777241871
CDS Mutation	c.1250C>T
AA Mutation	p.Thr417Met(p.T417M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000294702
Start	92476047:92476047(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757855720
CDS Mutation	c.1251G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> GFI1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000294702
Start	92481056:92481056(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.331G>A
AA Mutation	p.Glu111Lys(p.E111K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000294702
Start	92483047:92483047(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.116-1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript