Colon Cancer: Gene >> PPIG

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000260970
Start	169630942:169630942(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200547187
CDS Mutation	c.716G>A
AA Mutation	p.Arg239Gln(p.R239Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000260970
Start	169636838:169636838(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1580G>A
AA Mutation	p.Ser527Asn(p.S527N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000260970
Start	169608757:169608757(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.376A>G
AA Mutation	p.Ile126Val(p.I126V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000260970
Start	169636705:169636705(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1447A>C
AA Mutation	p.Lys483Gln(p.K483Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000260970
Start	169604067:169604067(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.26G>A
AA Mutation	p.Arg9Gln(p.R9Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000260970
Start	169636535:169636535(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1277T>G
AA Mutation	p.Val426Gly(p.V426G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000260970
Start	169636569:169636569(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1311C>G
AA Mutation	p.Asp437Glu(p.D437E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000260970
Start	169636542:169636542(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1284C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000260970
Start	169636512:169636512(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1259delA
AA Mutation	p.Asn420MetfsTer33(p.N420Mfs*33)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000260970
Start	169604071:169604071(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.36delT
AA Mutation	p.Phe12LeufsTer115(p.F12Lfs*115)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> PPIG

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000260970
Start	169636952:169636952(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746155807
CDS Mutation	c.1694G>A
AA Mutation	p.Arg565Gln(p.R565Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000260970
Start	169630947:169630947(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.721C>A
AA Mutation	p.His241Asn(p.H241N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript