Colon Cancer: Gene >> CAPN1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000279247
Start	65209358:65209358(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1765T>C
AA Mutation	p.Ser589Pro(p.S589P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000279247
Start	65186262:65186262(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748491783
CDS Mutation	c.683G>A
AA Mutation	p.Arg228His(p.R228H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000279247
Start	65209364:65209364(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750102134
CDS Mutation	c.1771C>T
AA Mutation	p.Arg591Cys(p.R591C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000279247
Start	65204728:65204728(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769161725
CDS Mutation	c.1211C>T
AA Mutation	p.Thr404Met(p.T404M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000279247
Start	65186255:65186255(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.676G>A
AA Mutation	p.Glu226Lys(p.E226K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000279247
Start	65204819:65204819(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1302C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000279247
Start	65206516:65206516(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745365536
CDS Mutation	c.1407G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000279247
Start	65183134:65183134(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.274C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000279247
Start	65210056:65210056(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1902C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> CAPN1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000279247
Start	65210849:65210849(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2095G>T
AA Mutation	p.Val699Phe(p.V699F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000279247
Start	65187223:65187223(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs534960869
CDS Mutation	c.768C>T
Mutation Classification	Silent
Feature Type	Transcript