Colon Cancer: Gene >> CPQ

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000220763
Start	96879896:96879896(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.740C>A
AA Mutation	p.Ser247Tyr(p.S247Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000220763
Start	96785195:96785195(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.298C>G
AA Mutation	p.Leu100Val(p.L100V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000220763
Start	97143054:97143054(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1290C>A
AA Mutation	p.Phe430Leu(p.F430L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000220763
Start	97029457:97029457(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1016G>A
AA Mutation	p.Gly339Asp(p.G339D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000220763
Start	96966002:96966002(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.917G>A
AA Mutation	p.Gly306Glu(p.G306E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000220763
Start	97029408:97029408(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753340797
CDS Mutation	c.967C>T
AA Mutation	p.Arg323Cys(p.R323C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000220763
Start	96834981:96834981(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767885584
CDS Mutation	c.442G>A
AA Mutation	p.Ala148Thr(p.A148T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000220763
Start	96784916:96784916(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs183172032
CDS Mutation	c.19G>A
AA Mutation	p.Ala7Thr(p.A7T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000220763
Start	97066138:97066138(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1183C>T
AA Mutation	p.Leu395Phe(p.L395F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000220763
Start	96785200:96785200(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.303G>T
AA Mutation	p.Glu101Asp(p.E101D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000220763
Start	96879860:96879860(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139595101
CDS Mutation	c.704C>T
AA Mutation	p.Thr235Met(p.T235M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000220763
Start	97029483:97029483(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1042C>A
AA Mutation	p.Gln348Lys(p.Q348K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000220763
Start	97143044:97143044(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1280A>G
AA Mutation	p.Tyr427Cys(p.Y427C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000220763
Start	96879901:96879901(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.745G>T
AA Mutation	p.Gly249Trp(p.G249W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000220763
Start	96835018:96835018(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.479A>G
AA Mutation	p.Gln160Arg(p.Q160R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000220763
Start	96784924:96784924(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746815323
CDS Mutation	c.27C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	stop_gained
Transcription ID	ENST00000220763
Start	97143160:97143160(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1396G>T
AA Mutation	p.Glu466Ter(p.E466*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> CPQ

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000220763
Start	96785042:96785042(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.145G>A
AA Mutation	p.Ala49Thr(p.A49T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000220763
Start	97143054:97143054(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1290C>A
AA Mutation	p.Phe430Leu(p.F430L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000220763
Start	96784983:96784983(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.86C>A
AA Mutation	p.Ser29Tyr(p.S29Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000220763
Start	96784989:96784989(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.92G>T
AA Mutation	p.Arg31Met(p.R31M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000220763
Start	97143054:97143054(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1290C>T
Mutation Classification	Silent
Feature Type	Transcript