Colon Cancer: Gene >> ADH1A

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000209668
Start	99284399:99284399(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.567G>T
AA Mutation	p.Lys189Asn(p.K189N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000209668
Start	99280251:99280251(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.857C>T
AA Mutation	p.Ala286Val(p.A286V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000209668
Start	99280171:99280171(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764209859
CDS Mutation	c.937C>T
AA Mutation	p.Arg313Cys(p.R313C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000209668
Start	99282606:99282606(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.568G>A
AA Mutation	p.Val190Ile(p.V190I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000209668
Start	99286952:99286952(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.157G>A
AA Mutation	p.Val53Met(p.V53M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000209668
Start	99282541:99282541(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772534129
CDS Mutation	c.633C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000209668
Start	99282508:99282508(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs61732104
CDS Mutation	c.666G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000209668
Start	99279566:99279566(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.965-2A>C
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> ADH1A

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000209668
Start	99287565:99287565(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.119A>T
AA Mutation	p.Lys40Met(p.K40M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript