Colon Cancer: Gene >> GLIPR1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000266659
Start	75482045:75482045(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139100030
CDS Mutation	c.386G>A
AA Mutation	p.Arg129Gln(p.R129Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000266659
Start	75481862:75481862(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.203C>T
AA Mutation	p.Ala68Val(p.A68V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000266659
Start	75481040:75481040(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.160G>T
AA Mutation	p.Asp54Tyr(p.D54Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000266659
Start	75480918:75480918(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773209636
CDS Mutation	c.38C>A
AA Mutation	p.Ser13Tyr(p.S13Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000266659
Start	75498721:75498721(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760377605
CDS Mutation	c.646+1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> GLIPR1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000266659
Start	75480965:75480965(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760375651
CDS Mutation	c.85G>A
AA Mutation	p.Glu29Lys(p.E29K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000266659
Start	75490511:75490511(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.526G>A
AA Mutation	p.Gly176Arg(p.G176R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000266659
Start	75480918:75480918(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773209636
CDS Mutation	c.38C>A
AA Mutation	p.Ser13Tyr(p.S13Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000266659
Start	75490438:75490438(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759292590
CDS Mutation	c.453C>T
Mutation Classification	Silent
Feature Type	Transcript