Colon Cancer: Gene >> PEX12

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000225873
Start	35576049:35576049(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.813A>C
AA Mutation	p.Glu271Asp(p.E271D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000225873
Start	35577366:35577366(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773708442
CDS Mutation	c.352A>G
AA Mutation	p.Met118Val(p.M118V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000225873
Start	35576040:35576040(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.822G>T
AA Mutation	p.Lys274Asn(p.K274N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000225873
Start	35577179:35577179(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745420734
CDS Mutation	c.539G>A
AA Mutation	p.Arg180Gln(p.R180Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000225873
Start	35576124:35576124(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.738C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000225873
Start	35576025:35576025(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.837G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000225873
Start	35577296:35577297(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.421dupG
AA Mutation	p.Asp141GlyfsTer2(p.D141Gfs*2)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000225873
Start	35576039:35576040(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.822_823insAACAGTA
AA Mutation	p.Ser275AsnfsTer19(p.S275Nfs*19)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> PEX12

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000225873
Start	35577179:35577179(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745420734
CDS Mutation	c.539G>A
AA Mutation	p.Arg180Gln(p.R180Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000225873
Start	35577446:35577446(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.272G>T
AA Mutation	p.Arg91Ile(p.R91I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript