Colon Cancer: Gene >> AKR1B1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000285930
Start	134445288:134445288(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.858G>T
AA Mutation	p.Met286Ile(p.M286I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000285930
Start	134448009:134448009(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770279911
CDS Mutation	c.712G>A
AA Mutation	p.Ala238Thr(p.A238T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000285930
Start	134451698:134451698(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.122G>A
AA Mutation	p.Arg41His(p.R41H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000285930
Start	134445247:134445247(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755184764
CDS Mutation	c.899C>T
AA Mutation	p.Ala300Val(p.A300V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000285930
Start	134459034:134459034(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs577826776
CDS Mutation	c.29G>A
AA Mutation	p.Gly10Asp(p.G10D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000285930
Start	134447342:134447342(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.781A>T
AA Mutation	p.Ile261Phe(p.I261F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000285930
Start	134447317:134447317(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.806G>A
AA Mutation	p.Arg269His(p.R269H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000285930
Start	134449018:134449018(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778492841
CDS Mutation	c.531G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000285930
Start	134448431:134448431(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs188664638
CDS Mutation	c.615C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> AKR1B1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000285930
Start	134449775:134449775(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.374T>C
AA Mutation	p.Leu125Ser(p.L125S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000285930
Start	134449743:134449743(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.406A>T
AA Mutation	p.Thr136Ser(p.T136S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000285930
Start	134442752:134442752(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.927T>G
AA Mutation	p.Asp309Glu(p.D309E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000285930
Start	134447307:134447307(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.816G>T
AA Mutation	p.Glu272Asp(p.E272D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000285930
Start	134451709:134451709(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758567690
CDS Mutation	c.111C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_gained
Transcription ID	ENST00000285930
Start	134448459:134448459(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.587T>G
AA Mutation	p.Leu196Ter(p.L196*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript