Colon Cancer: Gene >> FOXA1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000250448
Start	37591946:37591946(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.838A>G
AA Mutation	p.Ser280Gly(p.S280G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000250448
Start	37592260:37592260(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.524A>G
AA Mutation	p.Tyr175Cys(p.Y175C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000250448
Start	37591973:37591973(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.811C>A
AA Mutation	p.Gln271Lys(p.Q271K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000250448
Start	37592673:37592673(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.111C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000250448
Start	37592686:37592687(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.97_98insTAGG
AA Mutation	p.Asn33IlefsTer195(p.N33Ifs*195)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> FOXA1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000250448
Start	37592510:37592510(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.274G>A
AA Mutation	p.Ala92Thr(p.A92T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000250448
Start	37592427:37592427(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.357G>A
Mutation Classification	Silent
Feature Type	Transcript