Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> PPP6C

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000373547
Start	125153650:125153650(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.552A>C
AA Mutation	p.Glu184Asp(p.E184D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000373547
Start	125189644:125189644(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.75G>C
AA Mutation	p.Lys25Asn(p.K25N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000373547
Start	125149891:125149891(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.700T>G
AA Mutation	p.Cys234Gly(p.C234G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000373547
Start	125189663:125189663(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.56T>G
AA Mutation	p.Leu19Arg(p.L19R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000373547
Start	125153609:125153609(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.593A>C
AA Mutation	p.Asp198Ala(p.D198A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373547
Start	125149688:125149688(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749555521
CDS Mutation	c.903G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> PPP6C

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000373547
Start	125149867:125149867(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.724G>A
AA Mutation	p.Glu242Lys(p.E242K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000373547
Start	125153664:125153664(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781486938
CDS Mutation	c.538G>A
AA Mutation	p.Glu180Lys(p.E180K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000373547
Start	125149857:125149857(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.734A>C
AA Mutation	p.Lys245Thr(p.K245T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	stop_gained
Transcription ID	ENST00000373547
Start	125153673:125153673(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.529C>T
AA Mutation	p.Arg177Ter(p.R177*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript