Colon Cancer: Gene >> CAPN9

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000271971
Start	230779074:230779074(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145226005
CDS Mutation	c.1055C>T
AA Mutation	p.Thr352Met(p.T352M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000271971
Start	230772024:230772024(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375897039
CDS Mutation	c.800G>A
AA Mutation	p.Arg267Gln(p.R267Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000271971
Start	230792913:230792913(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1855G>A
AA Mutation	p.Ala619Thr(p.A619T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000271971
Start	230791921:230791921(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1715T>C
AA Mutation	p.Leu572Pro(p.L572P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000271971
Start	230769233:230769233(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.759T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000271971
Start	230779112:230779112(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1097delG
AA Mutation	p.Gly366AlafsTer15(p.G366Afs*15)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000271971
Start	230755345:230755346(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.227dupA
AA Mutation	p.Asn76LysfsTer13(p.N76Kfs*13)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> CAPN9

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000271971
Start	230792430:230792430(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1727G>A
AA Mutation	p.Ser576Asn(p.S576N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript