Colon Cancer: Gene >> P4HB

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000331483
Start	81855192:81855192(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.574G>A
AA Mutation	p.Val192Met(p.V192M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000331483
Start	81846626:81846626(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.859C>A
AA Mutation	p.Leu287Met(p.L287M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000331483
Start	81859273:81859273(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.260A>T
AA Mutation	p.Glu87Val(p.E87V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000331483
Start	81845634:81845634(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1286C>T
AA Mutation	p.Ala429Val(p.A429V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000331483
Start	81845616:81845616(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1304T>G
AA Mutation	p.Val435Gly(p.V435G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000331483
Start	81845724:81845724(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1196A>G
AA Mutation	p.His399Arg(p.H399R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000331483
Start	81855273:81855273(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.493G>A
AA Mutation	p.Glu165Lys(p.E165K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000331483
Start	81846534:81846534(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765631122
CDS Mutation	c.951C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000331483
Start	81845654:81845654(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs184374096
CDS Mutation	c.1266C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000331483
Start	81845888:81845888(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs773547908
CDS Mutation	c.1160delA
AA Mutation	p.Asn387ThrfsTer118(p.N387Tfs*118)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000331483
Start	81845143:81845143(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1446+1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> P4HB

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000331483
Start	81855540:81855540(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370423809
CDS Mutation	c.399G>A
Mutation Classification	Silent
Feature Type	Transcript