Colon Cancer: Gene >> PABPC4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000372857
Start	39572556:39572556(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.224A>G
AA Mutation	p.Asp75Gly(p.D75G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000372857
Start	39572532:39572532(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.248G>A
AA Mutation	p.Arg83His(p.R83H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000372857
Start	39565340:39565340(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1011C>A
AA Mutation	p.Phe337Leu(p.F337L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000372857
Start	39572412:39572412(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.368G>A
AA Mutation	p.Gly123Glu(p.G123E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000372857
Start	39567762:39567762(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.961A>G
AA Mutation	p.Thr321Ala(p.T321A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000372857
Start	39575846:39575846(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.106C>T
AA Mutation	p.Pro36Ser(p.P36S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000372857
Start	39564480:39564480(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1396G>A
AA Mutation	p.Ala466Thr(p.A466T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000372857
Start	39571284:39571284(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376599175
CDS Mutation	c.453C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000372857
Start	39575886:39575886(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201169120
CDS Mutation	c.66C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000372857
Start	39563873:39563873(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1455C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000372857
Start	39567843:39567843(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.880delG
AA Mutation	p.Val294Ter(p.V294*)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> PABPC4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000372857
Start	39568845:39568845(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749537752
CDS Mutation	c.833G>A
AA Mutation	p.Arg278Gln(p.R278Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000372857
Start	39564488:39564488(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139185037
CDS Mutation	c.1388G>A
AA Mutation	p.Arg463His(p.R463H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript