Colon Cancer: Gene >> FOXA2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000377115
Start	22582515:22582515(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760812511
CDS Mutation	c.709C>T
AA Mutation	p.Pro237Ser(p.P237S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000377115
Start	22582824:22582824(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.400A>C
AA Mutation	p.Ser134Arg(p.S134R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000377115
Start	22583138:22583138(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.86G>T
AA Mutation	p.Ser29Ile(p.S29I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000377115
Start	22582679:22582679(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.545T>A
AA Mutation	p.Leu182Gln(p.L182Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000377115
Start	22582634:22582634(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372773557
CDS Mutation	c.590G>A
AA Mutation	p.Arg197Gln(p.R197Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000377115
Start	22581873:22581873(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1351C>T
AA Mutation	p.Arg451Trp(p.R451W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> FOXA2

Mutation ID	1
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000377115
Start	22583155:22583155(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.70-1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript