Colon Cancer: Gene >> PON2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000222572
Start	95407021:95407021(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.743A>G
AA Mutation	p.Glu248Gly(p.E248G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000222572
Start	95409977:95409977(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.619T>C
AA Mutation	p.Tyr207His(p.Y207H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000222572
Start	95412418:95412418(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.261G>T
AA Mutation	p.Met87Ile(p.M87I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000222572
Start	95406165:95406165(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.860G>A
AA Mutation	p.Gly287Asp(p.G287D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000222572
Start	95405423:95405423(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.972G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000222572
Start	95411658:95411658(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs546665604
CDS Mutation	c.489T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000222572
Start	95405462:95405465(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.930_933delATCT
AA Mutation	p.Ser311ArgfsTer5(p.S311Rfs*5)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000222572
Start	95416248:95416248(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.195delT
AA Mutation	p.Phe65LeufsTer5(p.F65Lfs*5)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	stop_gained
Transcription ID	ENST00000222572
Start	95409993:95409993(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.603G>A
AA Mutation	p.Trp201Ter(p.W201*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> PON2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000222572
Start	95411705:95411705(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.442G>A
AA Mutation	p.Ala148Thr(p.A148T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	stop_gained
Transcription ID	ENST00000222572
Start	95409965:95409965(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.631G>T
AA Mutation	p.Glu211Ter(p.E211*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript