Colon Cancer: Gene >> AMELX

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000380714
Start	11298782:11298782(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.379T>C
AA Mutation	p.Tyr127His(p.Y127H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000380714
Start	11298862:11298862(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201127558
CDS Mutation	c.459G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000380714
Start	11298899:11298899(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.499delC
AA Mutation	p.Leu167CysfsTer8(p.L167Cfs*8)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000380714
Start	11298788:11298788(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.388delC
AA Mutation	p.Gln130SerfsTer45(p.Q130Sfs*45)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> AMELX

No Mutation Annotation!