Colon Cancer: Gene >> ALDH8A1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000265605
Start	134950038:134950038(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150345681
CDS Mutation	c.16G>A
AA Mutation	p.Ala6Thr(p.A6T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000265605
Start	134950003:134950003(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.51A>C
AA Mutation	p.Lys17Asn(p.K17N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000265605
Start	134918466:134918466(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1413G>T
AA Mutation	p.Lys471Asn(p.K471N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000265605
Start	134943904:134943904(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.201G>T
AA Mutation	p.Gln67His(p.Q67H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000265605
Start	134929129:134929129(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.936A>T
AA Mutation	p.Arg312Ser(p.R312S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000265605
Start	134942451:134942451(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.400C>A
AA Mutation	p.Leu134Met(p.L134M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000265605
Start	134932901:134932901(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.724C>A
AA Mutation	p.Leu242Met(p.L242M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000265605
Start	134942456:134942456(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.395A>T
AA Mutation	p.Asp132Val(p.D132V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265605
Start	134943874:134943874(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs568113669
CDS Mutation	c.231G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> ALDH8A1

No Mutation Annotation!