Colon Cancer: Gene >> ALDH6A1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000553458
Start	74072289:74072289(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374367200
CDS Mutation	c.262C>T
AA Mutation	p.Arg88Cys(p.R88C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000553458
Start	74065329:74065329(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1256T>C
AA Mutation	p.Phe419Ser(p.F419S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000553458
Start	74072222:74072222(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.329A>C
AA Mutation	p.Gln110Pro(p.Q110P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000553458
Start	74071445:74071445(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.480G>T
AA Mutation	p.Met160Ile(p.M160I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000553458
Start	74071899:74071899(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.424C>A
AA Mutation	p.Leu142Ile(p.L142I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> ALDH6A1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000553458
Start	74067514:74067514(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376852895
CDS Mutation	c.908A>G
AA Mutation	p.Asn303Ser(p.N303S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000553458
Start	74068905:74068905(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.807C>A
Mutation Classification	Silent
Feature Type	Transcript