Colon Cancer: Gene >> CELA1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000293636
Start	51342635:51342635(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.266A>G
AA Mutation	p.Tyr89Cys(p.Y89C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000293636
Start	51341327:51341327(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.380T>G
AA Mutation	p.Val127Gly(p.V127G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000293636
Start	51342684:51342684(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.217G>C
AA Mutation	p.Val73Leu(p.V73L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000293636
Start	51343760:51343760(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778795147
CDS Mutation	c.193G>A
AA Mutation	p.Val65Met(p.V65M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000293636
Start	51329750:51329750(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.693C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000293636
Start	51329820:51329820(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.623delG
AA Mutation	p.Gly208AlafsTer7(p.G208Afs*7)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> CELA1

No Mutation Annotation!