Colon Cancer: Gene >> ALDH2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000261733
Start	111790444:111790444(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.563C>A
AA Mutation	p.Pro188Gln(p.P188Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000261733
Start	111791364:111791364(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.740C>T
AA Mutation	p.Ala247Val(p.A247V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000261733
Start	111790533:111790533(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377123780
CDS Mutation	c.652G>A
AA Mutation	p.Ala218Thr(p.A218T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000261733
Start	111790452:111790452(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.571A>G
AA Mutation	p.Met191Val(p.M191V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000261733
Start	111785320:111785320(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.414T>G
AA Mutation	p.Asp138Glu(p.D138E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000261733
Start	111790512:111790512(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.631G>A
AA Mutation	p.Ala211Thr(p.A211T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> ALDH2

No Mutation Annotation!