Colon Cancer: Gene >> APIP

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000395787
Start	34895014:34895014(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.154C>T
AA Mutation	p.His52Tyr(p.H52Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000395787
Start	34888759:34888759(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.318A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000395787
Start	34883369:34883369(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.597G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000395787
Start	34888794:34888794(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs768283418
CDS Mutation	c.283delA
AA Mutation	p.Ser95AlafsTer8(p.S95Afs*8)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000395787
Start	34883359:34883359(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.607delA
AA Mutation	p.Thr203HisfsTer22(p.T203Hfs*22)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> APIP

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000395787
Start	34883394:34883394(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.572T>A
AA Mutation	p.Leu191Gln(p.L191Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript