Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> PPP1R2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000618156
Start	195523751:195523751(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751525820
CDS Mutation	c.344G>A
AA Mutation	p.Arg115Gln(p.R115Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000618156
Start	195524873:195524873(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.254C>T
AA Mutation	p.Ala85Val(p.A85V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000618156
Start	195524840:195524840(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.287C>T
AA Mutation	p.Ala96Val(p.A96V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000618156
Start	195529859:195529859(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs115915080
CDS Mutation	c.165G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000618156
Start	195519179:195519179(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.410delA
AA Mutation	p.Lys137SerfsTer6(p.K137Sfs*6)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_gained
Transcription ID	ENST00000618156
Start	195519177:195519177(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.412C>T
AA Mutation	p.Arg138Ter(p.R138*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> PPP1R2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000618156
Start	195523707:195523707(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.388T>A
AA Mutation	p.Ser130Thr(p.S130T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000618156
Start	195519108:195519108(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.481A>C
AA Mutation	p.Ile161Leu(p.I161L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000618156
Start	195519096:195519096(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.493C>A
AA Mutation	p.Leu165Ile(p.L165I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript