Colon Cancer: Gene >> AKR1C3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000380554
Start	5097453:5097453(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782497370
CDS Mutation	c.272G>A
AA Mutation	p.Arg91Gln(p.R91Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000380554
Start	5094469:5094469(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.25A>C
AA Mutation	p.Lys9Gln(p.K9Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000380554
Start	5099335:5099335(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.456G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	stop_gained
Transcription ID	ENST00000380554
Start	5096521:5096521(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782405598
CDS Mutation	c.196C>T
AA Mutation	p.Arg66Ter(p.R66*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> AKR1C3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000380554
Start	5096570:5096570(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.245C>A
AA Mutation	p.Thr82Asn(p.T82N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000380554
Start	5094476:5094476(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.32A>C
AA Mutation	p.Asn11Thr(p.N11T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000380554
Start	5105627:5105627(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs1804059
CDS Mutation	c.879G>T
AA Mutation	p.Met293Ile(p.M293I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript