Colon Cancer: Gene >> PPP1R18

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000274853
Start	30685523:30685523(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.496C>A
AA Mutation	p.Pro166Thr(p.P166T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000274853
Start	30685130:30685130(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753123312
CDS Mutation	c.889G>A
AA Mutation	p.Glu297Lys(p.E297K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000274853
Start	30685651:30685651(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.368G>A
AA Mutation	p.Arg123Lys(p.R123K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000274853
Start	30685930:30685930(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200269206
CDS Mutation	c.89G>A
AA Mutation	p.Arg30Gln(p.R30Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000274853
Start	30685732:30685732(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775362882
CDS Mutation	c.287A>G
AA Mutation	p.Gln96Arg(p.Q96R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000274853
Start	30685735:30685735(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.284G>A
AA Mutation	p.Arg95Gln(p.R95Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000274853
Start	30684425:30684425(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs555488215
CDS Mutation	c.1594G>A
AA Mutation	p.Glu532Lys(p.E532K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000274853
Start	30684468:30684468(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1551C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000274853
Start	30679213:30679213(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1788C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000274853
Start	30684642:30684642(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1377G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	stop_gained
Transcription ID	ENST00000274853
Start	30679212:30679212(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1789C>T
AA Mutation	p.Gln597Ter(p.Q597*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> PPP1R18

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000274853
Start	30685111:30685111(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.908C>T
AA Mutation	p.Ala303Val(p.A303V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000274853
Start	30685554:30685554(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.465G>T
Mutation Classification	Silent
Feature Type	Transcript