Colon Cancer: Gene >> LDLRAP1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000374338
Start	25553934:25553934(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.101A>G
AA Mutation	p.Asn34Ser(p.N34S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000374338
Start	25554000:25554000(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752849346
CDS Mutation	c.167C>T
AA Mutation	p.Thr56Met(p.T56M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000374338
Start	25565200:25565200(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.775T>C
AA Mutation	p.Phe259Leu(p.F259L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374338
Start	25563719:25563719(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.675G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000374338
Start	25563141:25563141(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.604delT
AA Mutation	p.Ser202ProfsTer2(p.S202Pfs*2)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000374338
Start	25563718:25563718(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.674delC
AA Mutation	p.Thr225ArgfsTer18(p.T225Rfs*18)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> LDLRAP1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000374338
Start	25562697:25562697(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.513T>G
AA Mutation	p.Phe171Leu(p.F171L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374338
Start	25566959:25566959(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747886166
CDS Mutation	c.894C>T
Mutation Classification	Silent
Feature Type	Transcript