Colon Cancer: Gene >> PI15

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000260113
Start	74845403:74845403(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145048888
CDS Mutation	c.547C>T
AA Mutation	p.Arg183Trp(p.R183W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000260113
Start	74845442:74845442(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.586G>A
AA Mutation	p.Val196Ile(p.V196I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000260113
Start	74825437:74825437(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs192682386
CDS Mutation	c.188C>T
AA Mutation	p.Ser63Leu(p.S63L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000260113
Start	74844090:74844090(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200713288
CDS Mutation	c.383G>A
AA Mutation	p.Arg128His(p.R128H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000260113
Start	74825428:74825428(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.179G>A
AA Mutation	p.Arg60His(p.R60H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000260113
Start	74844072:74844072(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.365G>T
AA Mutation	p.Gly122Val(p.G122V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000260113
Start	74849152:74849152(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.676G>T
AA Mutation	p.Gly226Trp(p.G226W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	inframe_insertion
Transcription ID	ENST00000260113
Start	74849236:74849237(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.760_761insCATTTTTTAAAAGTAGAT
AA Mutation	p.Tyr253_Leu254insProPhePheLysSerArg(p.Y253_L254insPFFKSR)
Mutation Classification	In_Frame_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> PI15

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000260113
Start	74825316:74825316(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs529529830
CDS Mutation	c.67G>A
AA Mutation	p.Val23Ile(p.V23I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000260113
Start	74845226:74845226(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.491G>T
AA Mutation	p.Arg164Ile(p.R164I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000260113
Start	74825481:74825481(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.232C>T
AA Mutation	p.Arg78Trp(p.R78W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000260113
Start	74844085:74844085(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.378T>A
Mutation Classification	Silent
Feature Type	Transcript