Colon Cancer: Gene >> PRELP

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000343110
Start	203483491:203483491(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs571164341
CDS Mutation	c.307C>T
AA Mutation	p.Arg103Cys(p.R103C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000343110
Start	203484125:203484125(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.941A>G
AA Mutation	p.Glu314Gly(p.E314G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000343110
Start	203483617:203483617(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.433G>A
AA Mutation	p.Val145Met(p.V145M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000343110
Start	203483696:203483696(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749884978
CDS Mutation	c.512G>A
AA Mutation	p.Arg171Gln(p.R171Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000343110
Start	203484005:203484005(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.821A>G
AA Mutation	p.Asn274Ser(p.N274S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000343110
Start	203483268:203483268(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs562945346
CDS Mutation	c.84C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000343110
Start	203483829:203483829(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149672468
CDS Mutation	c.645C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000343110
Start	203486800:203486800(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1068G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000343110
Start	203483961:203483961(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370979066
CDS Mutation	c.777C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000343110
Start	203484102:203484102(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.918G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000343110
Start	203483421:203483421(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.242delC
AA Mutation	p.Pro81LeufsTer61(p.P81Lfs*61)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> PRELP

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000343110
Start	203483584:203483584(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.400G>T
AA Mutation	p.Asp134Tyr(p.D134Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000343110
Start	203486705:203486705(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.974-1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript