Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> PPP1R7

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000234038
Start	241158526:241158526(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.280T>G
AA Mutation	p.Phe94Val(p.F94V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000234038
Start	241153490:241153490(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777048169
CDS Mutation	c.67G>A
AA Mutation	p.Glu23Lys(p.E23K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000234038
Start	241182728:241182728(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758294774
CDS Mutation	c.988C>T
AA Mutation	p.Arg330Trp(p.R330W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000234038
Start	241163290:241163290(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs545930743
CDS Mutation	c.603C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000234038
Start	241182799:241182799(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775007848
CDS Mutation	c.1059C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000234038
Start	241157842:241157842(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.218delA
AA Mutation	p.Asn73ThrfsTer11(p.N73Tfs*11)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> PPP1R7

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000234038
Start	241163328:241163328(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.641T>G
AA Mutation	p.Phe214Cys(p.F214C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000234038
Start	241160407:241160407(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.510C>A
AA Mutation	p.Phe170Leu(p.F170L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000234038
Start	241153540:241153540(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200351113
CDS Mutation	c.117C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000234038
Start	241160368:241160368(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762600707
CDS Mutation	c.471C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000234038
Start	241182799:241182799(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775007848
CDS Mutation	c.1059C>T
Mutation Classification	Silent
Feature Type	Transcript