Colon Cancer: Gene >> ACPP

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000336375
Start	132337541:132337541(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.542T>C
AA Mutation	p.Leu181Pro(p.L181P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000336375
Start	132332202:132332202(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777654881
CDS Mutation	c.314G>A
AA Mutation	p.Arg105Gln(p.R105Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000336375
Start	132345011:132345011(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.733T>C
AA Mutation	p.Ser245Pro(p.S245P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000351273
Start	132367765:132367765(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1200G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000336375
Start	132352800:132352800(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.945G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000336375
Start	132352767:132352767(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376964687
CDS Mutation	c.912C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	inframe_insertion
Transcription ID	ENST00000336375
Start	132331724:132331725(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.294_295insTCACACTAT
AA Mutation	p.Lys98_His99insSerHisTyr(p.K98_H99insSHY)
Mutation Classification	In_Frame_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> ACPP

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000336375
Start	132352774:132352774(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.919C>T
AA Mutation	p.Leu307Phe(p.L307F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	stop_gained
Transcription ID	ENST00000336375
Start	132344987:132344987(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.709G>T
AA Mutation	p.Glu237Ter(p.E237*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	stop_gained
Transcription ID	ENST00000336375
Start	132332201:132332201(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758538660
CDS Mutation	c.313C>T
AA Mutation	p.Arg105Ter(p.R105*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	stop_gained
Transcription ID	ENST00000351273
Start	132367802:132367802(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1237G>T
AA Mutation	p.Glu413Ter(p.E413*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript