Colon Cancer: Gene >> ADH1C

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000515683
Start	99347040:99347040(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.225A>C
AA Mutation	p.Glu75Asp(p.E75D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000515683
Start	99344884:99344884(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.545G>A
AA Mutation	p.Gly182Glu(p.G182E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000515683
Start	99342989:99342989(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.634T>A
AA Mutation	p.Cys212Ser(p.C212S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000515683
Start	99342887:99342887(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.736G>T
AA Mutation	p.Asp246Tyr(p.D246Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000515683
Start	99342877:99342877(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.746A>T
AA Mutation	p.Lys249Ile(p.K249I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000515683
Start	99340587:99340587(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.952G>A
AA Mutation	p.Ala318Thr(p.A318T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	inframe_insertion
Transcription ID	ENST00000515683
Start	99343041:99343042(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.581_582insCTT
AA Mutation	p.Ser194_Thr195insPhe(p.S194_T195insF)
Mutation Classification	In_Frame_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> ADH1C

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000515683
Start	99342937:99342937(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.686A>C
AA Mutation	p.Lys229Thr(p.K229T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000515683
Start	99347808:99347808(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.57G>T
AA Mutation	p.Lys19Asn(p.K19N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript