Colon Cancer: Gene >> FOXF1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000262426
Start	86510778:86510778(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs568384890
CDS Mutation	c.209C>T
AA Mutation	p.Thr70Met(p.T70M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000262426
Start	86511093:86511093(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.524C>T
AA Mutation	p.Ser175Leu(p.S175L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000262426
Start	86510690:86510690(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.121G>A
AA Mutation	p.Ala41Thr(p.A41T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262426
Start	86510995:86510995(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.426C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262426
Start	86512950:86512950(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754997103
CDS Mutation	c.1005G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262426
Start	86510884:86510884(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.315C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262426
Start	86513046:86513046(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1101G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> FOXF1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000262426
Start	86510981:86510981(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.412C>T
AA Mutation	p.Arg138Trp(p.R138W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript