Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> PPP1R15A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000200453
Start	48873309:48873309(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.76A>C
AA Mutation	p.Met26Leu(p.M26L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000200453
Start	48874082:48874082(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.849A>T
AA Mutation	p.Glu283Asp(p.E283D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000200453
Start	48873636:48873636(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.403G>A
AA Mutation	p.Ala135Thr(p.A135T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000200453
Start	48873930:48873930(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.697G>A
AA Mutation	p.Glu233Lys(p.E233K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000200453
Start	48874145:48874145(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.912C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_gained
Transcription ID	ENST00000200453
Start	48873945:48873945(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.712G>T
AA Mutation	p.Glu238Ter(p.E238*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> PPP1R15A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000200453
Start	48874596:48874596(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1363G>A
AA Mutation	p.Asp455Asn(p.D455N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000200453
Start	48874758:48874758(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1525G>A
AA Mutation	p.Val509Met(p.V509M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000200453
Start	48874739:48874739(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1506T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	stop_gained
Transcription ID	ENST00000200453
Start	48874105:48874105(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.872C>A
AA Mutation	p.Ser291Ter(p.S291*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript