Colon Cancer: Gene >> PON1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000222381
Start	95315345:95315345(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.347G>T
AA Mutation	p.Gly116Val(p.G116V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000222381
Start	95308050:95308050(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.659T>C
AA Mutation	p.Phe220Ser(p.F220S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000222381
Start	95308018:95308018(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs564064745
CDS Mutation	c.691G>A
AA Mutation	p.Asp231Asn(p.D231N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000222381
Start	95302244:95302244(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.870A>C
AA Mutation	p.Lys290Asn(p.K290N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000222381
Start	95306341:95306341(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.724G>A
AA Mutation	p.Ala242Thr(p.A242T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000222381
Start	95299095:95299095(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749649413
CDS Mutation	c.917G>A
AA Mutation	p.Arg306Gln(p.R306Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000222381
Start	95306319:95306319(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.746A>G
AA Mutation	p.Glu249Gly(p.E249G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000222381
Start	95311492:95311492(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770941938
CDS Mutation	c.456G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000222381
Start	95324470:95324470(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753471724
CDS Mutation	c.6G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000222381
Start	95315439:95315439(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.253delA
AA Mutation	p.Ile85TyrfsTer3(p.I85Yfs*3)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	stop_gained
Transcription ID	ENST00000222381
Start	95308069:95308069(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.640C>T
AA Mutation	p.Arg214Ter(p.R214*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	stop_gained
Transcription ID	ENST00000222381
Start	95318389:95318389(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs565598241
CDS Mutation	c.79C>T
AA Mutation	p.Arg27Ter(p.R27*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000222381
Start	95311457:95311459(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.489_491delTCT
AA Mutation	p.Leu164del(p.L164del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript

Rectum Cancer: Gene >> PON1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000222381
Start	95299095:95299095(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749649413
CDS Mutation	c.917G>A
AA Mutation	p.Arg306Gln(p.R306Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000222381
Start	95308018:95308018(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs564064745
CDS Mutation	c.691G>A
AA Mutation	p.Asp231Asn(p.D231N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript