Colon Cancer: Gene >> ZMPSTE24

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000372759
Start	40267870:40267870(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.355G>A
AA Mutation	p.Glu119Lys(p.E119K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000372759
Start	40292476:40292476(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs555007253
CDS Mutation	c.1235G>A
AA Mutation	p.Arg412His(p.R412H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000372759
Start	40260968:40260968(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.253T>G
AA Mutation	p.Ser85Ala(p.S85A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000372759
Start	40290861:40290861(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1067C>A
AA Mutation	p.Ser356Tyr(p.S356Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000372759
Start	40260852:40260852(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763658936
CDS Mutation	c.137A>C
AA Mutation	p.Lys46Thr(p.K46T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000372759
Start	40268464:40268464(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.403G>A
AA Mutation	p.Ala135Thr(p.A135T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000372759
Start	40281485:40281485(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.912T>C
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> ZMPSTE24

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000372759
Start	40270007:40270007(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.507G>T
AA Mutation	p.Lys169Asn(p.K169N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	stop_gained
Transcription ID	ENST00000372759
Start	40281507:40281507(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.934G>T
AA Mutation	p.Glu312Ter(p.E312*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript