Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> PEG10

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000482108
Start	94663903:94663903(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.347T>C
AA Mutation	p.Val116Ala(p.V116A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000482108
Start	94663690:94663690(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.134G>A
AA Mutation	p.Arg45Gln(p.R45Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000482108
Start	94663939:94663939(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.383G>A
AA Mutation	p.Arg128His(p.R128H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000482108
Start	94664225:94664225(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.669C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000482108
Start	94664312:94664312(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775882612
CDS Mutation	c.756G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000482108
Start	94664402:94664402(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769024582
CDS Mutation	c.846G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	stop_gained
Transcription ID	ENST00000482108
Start	94663566:94663566(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.10C>T
AA Mutation	p.Arg4Ter(p.R4*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> PEG10

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000482108
Start	94664080:94664080(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.524G>A
AA Mutation	p.Arg175His(p.R175H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000482108
Start	94664074:94664074(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774623837
CDS Mutation	c.518G>A
AA Mutation	p.Arg173His(p.R173H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000482108
Start	94664395:94664395(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs556674678
CDS Mutation	c.839G>A
AA Mutation	p.Arg280His(p.R280H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript