Colon Cancer: Gene >> PABPC1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000318607
Start	100712695:100712695(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.833G>A
AA Mutation	p.Arg278His(p.R278H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000318607
Start	100712390:100712390(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.944C>T
AA Mutation	p.Ser315Phe(p.S315F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000318607
Start	100706767:100706767(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1486G>A
AA Mutation	p.Ala496Thr(p.A496T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000318607
Start	100704996:100704996(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1748G>A
AA Mutation	p.Gly583Asp(p.G583D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000318607
Start	100712705:100712705(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.823G>A
AA Mutation	p.Glu275Lys(p.E275K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000318607
Start	100718227:100718227(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.247C>T
AA Mutation	p.Arg83Cys(p.R83C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000318607
Start	100721518:100721518(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.66G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000318607
Start	100704980:100704980(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1764T>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	stop_gained
Transcription ID	ENST00000318607
Start	100715540:100715540(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.565G>T
AA Mutation	p.Glu189Ter(p.E189*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	stop_gained;protein_altering_variant
Transcription ID	ENST00000318607
Start	100705032:100705033(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1711_1712insCATAAA
AA Mutation	p.Gln571delinsProTerLys(p.Q571delinsP*K)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> PABPC1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000318607
Start	100717779:100717779(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.497G>A
AA Mutation	p.Arg166His(p.R166H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	stop_gained
Transcription ID	ENST00000318607
Start	100715540:100715540(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.565G>T
AA Mutation	p.Glu189Ter(p.E189*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript