Colon Cancer: Gene >> PON3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000265627
Start	95372285:95372285(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.255C>G
AA Mutation	p.Ile85Met(p.I85M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000265627
Start	95360125:95360125(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.913C>T
AA Mutation	p.Arg305Cys(p.R305C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000265627
Start	95363974:95363974(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.584T>C
AA Mutation	p.Met195Thr(p.M195T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000265627
Start	95362825:95362825(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.712G>T
AA Mutation	p.Asp238Tyr(p.D238Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000265627
Start	95372322:95372322(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.218G>A
AA Mutation	p.Gly73Asp(p.G73D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000265627
Start	95396344:95396344(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.7A>G
AA Mutation	p.Lys3Glu(p.K3E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000265627
Start	95362451:95362451(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748765744
CDS Mutation	c.817G>A
AA Mutation	p.Asp273Asn(p.D273N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000265627
Start	95372220:95372220(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.320A>G
AA Mutation	p.Asp107Gly(p.D107G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000265627
Start	95363935:95363935(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749309125
CDS Mutation	c.623G>A
AA Mutation	p.Ser208Asn(p.S208N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000265627
Start	95362403:95362403(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.865A>G
AA Mutation	p.Lys289Glu(p.K289E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265627
Start	95390172:95390172(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778287055
CDS Mutation	c.183G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265627
Start	95372306:95372306(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377390399
CDS Mutation	c.234G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000265627
Start	95372340:95372340(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.202-2delA
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> PON3

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265627
Start	95362835:95362835(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.702C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265627
Start	95372180:95372180(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779151483
CDS Mutation	c.360C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000265627
Start	95372171:95372171(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.367+2T>C
Mutation Classification	Splice_Site
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	inframe_insertion
Transcription ID	ENST00000265627
Start	95372275:95372276(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.264_265insAATCTGAAT
AA Mutation	p.Met88_Asp89insAsnLeuAsn(p.M88_D89insNLN)
Mutation Classification	In_Frame_Ins
Feature Type	Transcript